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Novartis AG

Novartis bietet innovative medizinische Lösungen an, um damit auf die sich verändernden Bedürfnisse von Patienten und Gesellschaften einzugehen. Novartis, mit Hauptsitz in Basel (Schweiz), verfügt über ein diversifiziertes Portfolio, um diese Bedürfnisse so gut wie möglich zu erfüllen: mit innovativen Arzneimitteln, Produkten für die Augenheilkunde und kostengünstigen generischen Medikamenten. Novartis ist das einzige Unternehmen mit weltweit führenden Positionen in diesen Bereichen.

Novartis AG

Fabrikstrasse 2
4056Basel

08.08.2020

Novartis AG

Postdoctoral Scholar position Digital Endpoints in Neuroscience

  • Novartis AG

  • 4051Basel

  • 08.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID298395BRPosition TitlePostdoctoral Scholar position: Digital Endpoints in NeuroscienceApply to Job Job Description The Novartis Institutes for BioMedical Research (NIBR) is the innovation engine of Novartis. We collaborate across scientific and organizational boundaries, with a focus on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. The Quantitative Sciences and Innovation Group (link to mentor profile, if applicable) is seeking a strong candidate interested in sensor technologies, signal processing, data science and the brain. Development of digital endpoints is an important innovation effort at Novartis, because digital technologies provide unique opportunities for modernizing clinical research. In Neuroscience, the clinical outcome measures to assess functioning of CNS (central nervous system) are still based on pen and paper rating scales. These scales provide limited information, are highly variable and subject to rater bias. Consequently, there is a strong need for developing better, more accurate and robust measures of efficacy for CNS clinical trials. Digital endpoints are objective, quantifiable physiological and behavioral data that are collected and measured by means of digital devices such as portables, wearables, implantables or digestibles. Novartis is collecting huge amounts of digital biomarker data and we are searching for a candidate enthusiastic to dive into the sensor data and help us develop more sensitive measures of CNS function. The successful candidate will join a vibrant scientific community and collaborate with other postdoctoral fellows mentored by a range of scientists across disciplines and platforms, including chemistry, structural biology, molecular biology, functional genomics, neurophysiology and translational medicine. Postdoctoral scholars at NIBR have a unique opportunity to conduct innovative, interdisciplinary research and are expected to publish their results in leading journals. The postdoctoral term is up to 4 years. #PDX Minimum requirements Qualifications:  PhD in biomedical engineering, signal processing, computer science, data science or statistics (PhD students in the last year of their thesis work, are eligible to apply)  Strong communication skills  Strong publication record  Excellent analytical, communication and organizational skills  Candidates must be able to work independently as well as with interdisciplinary teams For more information about our postdoctoral program, please visit https://www.novartis.com/our-science/postdoc-program. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionNIBRBusiness UnitTranslational MedicineLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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08.08.2020

Novartis AG

Global Head IP Litigation

  • Novartis AG

  • 4040Basel

  • 08.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID298363BRPosition TitleGlobal Head IP LitigationApply to Job Job Description 500! With over 500 active IP litigation in more than 50 countries, the Global Head IP Litigation for Novartis Group has the unique opportunity to coordinate, manage, and influence important patent and trademark matters around the world. This position facilitates collaboration and best practices for our team of dedicated and experienced litigators who design and implement the IP strategies needed for Novartis innovative medicine and generic products, all for the ultimate benefit of patients and society. The Global Head IP Litigation ensures a thoughtful balance of litigation with a respect for valid IP right so that Novartis advances as a reputational leader among pharmaceutical companies. As our Global Head IP Litigation, you will lead all IP and related activities within a large global business unit or functional area(s) across the franchises. You will act as a strategic partner for business leaders in the BU or Division on IP activities and strategy and be accountable for delivering the highest quality IP and related strategies. You will manage other managers and a large team of IP, Patent, Trademark and Operational associates and support staff. In addition, you will contribute significantly to the development of own Division and cross-divisional IP operational and strategic objectives. Your responsibilities will include: • Oversee, coordinate, and drive the strategy for significant complex IP disputes (including patent and trademark litigations, arbitrations, and investigations) throughout the Novartis Group, supporting the Divisions/Units in their IP disputes and analyze, by developing and delivering IP litigation and dispute resolution strategies (including settlement negotiations) in significant cases in line with business requirements. • Develop and drive the IP and regulatory litigation governance framework, establish appropriate tools and processes, and lead high-visibility, complex global IP and regulatory (EMA/FDA) litigation projects. • Advise the Global Head IP as well as senior business leaders on IP disputes and risk exposure, including strategies for minimizing adverse consequences from such disputes. • Coordinate the group-wide IP litigation SOX and internal reporting and public disclosures, including work with Investor Relations, and ensure quality and consistency of reporting. • Improve exchange of information and know-how cross-divisionally and provide training, with the goal that in-house lawyers take a consistent and proactive approach in effectively dealing with IP disputes. • Track and report on legislative developments and trends in the IP area, and use that insight to shape/influence policy and governance objectives, and to assist management to understand IP and regulatory litigation de Minimum requirements What you’ll bring to the role: • Law school graduate (Common or Civil Law), Common Law preferred. Patent attorney qualification preferred. • Fluency in English required; good knowledge of other main European language is an asset. • 15+ years (at least 5 years leading associates) proven litigation experience, with at least some exposure to US as well as EU and other ROW litigations. External litigation experience required. • Sound knowledge of related following disciplines: Regulatory, Antitrust. • Good basic understanding of related disciplines such as M&A, BD&L, Corporate, Tax. • Ability to analyze complex legal issues. • Strong verbal & written communication skills, together with a high ability to influence and negotiate. Proven ability to deal positively when working within tight time pressures and demanding clients. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionCORPORATEBusiness UnitGROUP LEGALLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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07.08.2020

Novartis AG

DataCenter Network Engineering Expert (80 -100%)

  • Novartis AG

  • 4040Basel

  • 07.08.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID298930BRPosition TitleDataCenter Network Engineering Expert (80 -100%)Apply to Job Job Description DataCenter Network Engineering Expert (80 -100%) 1 Tbps ! The core IT network here in Basel with around one Tera bit per second throughput and around 20,000 network ports is waiting for the right Person to continue its journey into our future of digital. This role is key for the future of our digital journey. Our datacenter network plays a key role for Novartis and is the base for all application on top of it. Continued stable Operations and implementation of new future capabilities will be a key part of the role. Your responsibilities include, but not limited to: • Design, implement and maintain security/infrastructure requirements for development / testing environment, OR design, implement and keep technology stack of relevant products for development • Work in close collaboration with Architecture and Operations to integrate new solutions, ensuring timely and cost-effective delivery of solutions required for new projects and high integration of components • Develop and enhance automated processes to release new solutions into the live environment or create reusable and automation frameworks. • Ensure controls are in place for all configuration items and only authorized changes are made for all assets within enterprise IT environment • Participate in after-hours upgrades, troubleshooting, and/or on-call availability as needed. Provides end-to-end analytical support to ensure the delivery of Service related requests. . • Can be asked to assist with the handling of major incidents and identifying their root causes. • Level 4 support for problems identified with systems and Network. Act as an escalation for Level 3 Managed Services support technicians. • Provide recommendations to internal Engineering team to increase effectiveness of technology solutions (CSI, continuous service improvement) Minimum requirements What you’ll bring to the role: • German IT Incident & Problem Management IT Service Acceptance IT Configuration & Asset Management Release & Deployment • University degree level education or comparable education in Computer Science or Engineering Science (technical background) • 10+ years of experience in the area of network engineering. • Desirable: ITIL v3 experience or foundation certification,Project Management experience or foundation certification CCNP, CCDP (highly desirable) o CCIE certifications (plus but not needed) • Operations Management and Execution Collaborating across boundaries • Complexity Influencing without authority Ambiguity Why Novartis 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis!DivisionNBSBusiness UnitIT NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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07.08.2020

Novartis AG

Senior Expert Data Scientist in Biopharmaceutics - Technical Research

  • Novartis AG

  • 4051Basel

  • 07.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID299552BRPosition TitleSenior Expert Data Scientist in Biopharmaceutics – Technical ResearchApply to Job Job Description 90! The number of New Molecular Entities currently in clinics awaiting to be transformed into successful high quality innovative medicines. Analytical R&D (ARD) sits within the Global Technical R&D department of Global Drug Development. ARD plays an essential role in the characterization and analysis of small molecule drug substances and drug products from the time they leave the discovery laboratory until they are transferred to commercial production. We are looking for a highly motivated Senior Expert Data Scientist with a strong background and experience in biopharmaceutics assessments. Your responsibilities include but are not limited to: • Lead and execute biopharmaceutics assessments for oral and parenteral dosage forms • Establish Physiologically Based Pharmacokinetic (PBPK) models in the early and late phase of pharmaceutical development • Operate within internal networks of experts and participate in external research initiatives • Accountable to meet quality, timelines and budget for assigned deliverables • Support and guide the design of experimental work and interact with lab scientists • Ensures the distribution of lessons learned and scientific know-how within and across units • Strong contribution to advanced science, technology and innovation within ARD Minimum requirements What you’ll bring to the role: • BS / MS in pharmaceutical sciences or in analytical chemistry with minimum 1-3 years’ experience in industry focusing on biopharmaceutics, or PhD in biopharmaceutics or equivalent desirable • Proven experience and profound scientific knowledge in the drug physico-chemical characterization and the biorelevant dissolution testing of conventional and enabling formulations • Profound scientific knowledge in the formulation behavior following oral and parenteral drug administration and proven experience in PBPK absorption models (e.g. GastroPlus and Simcyp) • Knowledge in dissolution rate and related analytical technologies • Strong scientific focus • Fluent in English (oral and in writing) • Ability to perform in a highly dynamic environment Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaData & DigitalJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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07.08.2020

Novartis AG

Principal Scientist/Senior Principal Scientist, PK Sciences (80-100% )

  • Novartis AG

  • 4040Basel

  • 07.08.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID299530BRPosition TitlePrincipal Scientist/Senior Principal Scientist, PK Sciences (80-100%*)Apply to Job Job Description 48! That’s the number of projects Novartis Translational Medicine PK Sciences support in the Therapeutic Area of Autoimmune, Transplantation and Inflammation (ATI). PK Sciences provides PK and PKPD strategies from early discovery all the way through to registration and beyond. About half of the ATI portfolio represents biologics projects spanning from classical monoclonal antibodies to complex biologics constructs. We are looking for a new experienced team member who can join the PK Sciences team in our global mission to reimagine medicine. As a project team member you will provide PK expertise on biologics projects. Your Responsibilities will include but are not limited to: • Independently representing PK Sciences as a member of discovery, translational medicine and global project teams and leading PKS sub-teams to define PKS strategies for compound progression and development • Analyzing and interpreting PK//PD/IG data generated during discovery, early and full development; presenting results to the program • Proactively identifying potential project hurdles, providing solutions, and contributing to contingency plans • Authoring and preparing key clinical and regulatory documents including clinical study protocols, clinical study reports, modeling reports, investigator brochures, IND / IMPDs and NDAs while meeting all timescale and regulatory requirements • Publishing internally or externally as a main contributor to enhance the visibility of Novartis and PK Sciences Minimum requirements What you’ll bring to the role: • PhD, MD or PharmD in life sciences/healthcare with a focus on biologics therapies • Credible background and in depth knowledge of clinical pharmacology with significant drug discovery & development experience for biological drug candidates • Up-to-date background on state-of-the-art scientific and regulatory aspects of biologics drug development • Experience with standard PK analysis software (Phoenix) alongside understanding of applications of M&S techniques • Used to working in and adapting in line with the ever changing scientific and regulatory environment • A curious mind and strong interpersonal skills Desirable: • Previous experience in working in a cross-functional project team environment Why consider Novartis? 799 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionNIBRBusiness UnitTranslational MedicineLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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07.08.2020

Novartis AG

Quantitative Systems Pharmacologist-Snr/Principal Scientist (80-100% )

  • Novartis AG

  • 4051Basel

  • 07.08.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID299542BRPosition TitleQuantitative Systems Pharmacologist-Snr/Principal Scientist (80-100%*)Apply to Job Job Description 7! The number of sites globally where NIBR associates contribute to Novartis’ mission to reimagine medicine. NIBR is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Translational Medicine (TM) is the clinical research arm of NIBR, and includes about 1000 associates globally. TM plays a pivotal role in bringing innovative medicines to patients, by building on research advances to develop new therapies, and bridging drug discovery and clinical application. PK Sciences (PKS) partners across both NIBR and Global Drug Development organizations to advance the scientific knowledge of pharmacokinetics, metabolism and clinical pharmacology, and bring it to bear on drug discovery and development challenges throughout R&D. We are looking for a motivated individual to join PK Sciences as a Quantitative Systems Pharmacologist. The Modeling & Simulation function is embedded within PK Sciences and Translational Medicine. Our main objective is to enable quantitative and rigorous decision making at each stage of the process from target identification through to first-in-human studies. As a Quantitative systems pharmacologist you will always be looking for innovative ways modeling and simulation can be applied to drug discovery. Additionally you will understand experimental design, be a great communicator, a strong collaborator and highly self-motivated. As PK Sciences support all therapeutic modalities and therapeutic areas there are a lot of novel and exciting scientific questions to address. If you would like to help in shaping our function – come and join us! Responsibilities will include but are not limited to: • Identify high-impact research questions • Develop and apply a range of (innovative) modeling and simulation approaches to support and influence critical decisions in drug discovery and development across disease areas • Analyze, interpret, integrate, and report preclinical and clinical PK/PD data • Build multi-scale quantitative systems pharmacology models to address project questions and provide scenarios to the project team to guide decision making e.g. identify molecule design criteria based on early PK/PD understanding, biomarkers, influence combination strategies and optimize dose and dosing schedules. • Collaborate with colleagues from different quantitative disciplines • Participate in PKS and project sub-teams to define PKS strategy and experimental design to support compound progression and development. • Identify potential project hurdles, suggest solutions and contribute to contingency plans. • Publish or present internally or externally as a contributor to enhance Novartis and M&S visibility. Minimum requirements What you’ll bring to the role: • PhD in BioEngineering, Pharmaceutical Sciences, Mathematics, Physics or closely related field. Fluent in English. • Good understanding of cell biology and physiology • Experience working with large and/or complex datasets • Proficient in a scripting language (e.g. MATLAB, R, Python) and statistical software (JMP, R, etc.). Skilled in parameter estimation, mathematical problem solving, data analysis & visualization • Demonstrated ability to communicate modeling results to non-experts to facilitate strategy and decision-making • Demonstrated success in working cross-functional team in a highly dynamic, matrixed, project-team environment Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. *This role can be hired at Senior Scientist or Principal level dependent on relevant industry experience Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionNIBRBusiness UnitTranslational MedicineLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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06.08.2020

Novartis AG

Scientific Associate/Scientist, Cell Biology and Immunology (80-100 )

  • Novartis AG

  • 4051Basel

  • 06.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID298854BRPosition TitleScientific Associate/Scientist, Cell Biology and Immunology (80-100*)Apply to Job Job Description 6500! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. The Neuroscience (NS) Department at Novartis Institutes for Biomedical Research (NIBR) in Basel, Switzerland, is seeking a Scientific Associate or Scientist with Molecular and Cell Biology skills to join a lab focusing on neuroscience. The specific focus of the team is to modulate neuroinflammation to ameliorate or halt pathology in neurodegenerative diseases. As part of a multidisciplinary, highly collaborative team, you will independently plan, execute and analyze experiments and interpret data aiming at the discovery and characterization of new therapeutic targets and drug leads. The group is using complex primary cell culture models, but also establishing cellular high and medium throughput assays to assess therapeutic efficacy of antisense oligonucleotides, antibodies or low molecular weight compound under relevant physiological conditions. On top of a solid neurobiological background, good knowledge of and experience with immunological methods (FACS, cytokine assays, ELISA, histology) would be an asset. You will present data in meetings within the department and to contribute to writing of research documents and publications. Furthermore, you will interact with multiple groups within our department as well as with other groups and external colleagues and have the opportunity to represent the lab in project team meetings. Minimum requirements What you’ll bring to the role: • BSc or MSc in Neurobiology / Immunology or another relevant Life Science discipline, as well as Proficiency in English. Several years of work experience in industry or academia in drug discovery or related laboratory research • Proficiency in Molecular and Cell Biology techniques, comprising but not restricted to cultivation and manipulation of cell lines and primary mouse and human cell cultures, biochemical assays (e.g. cytokine assays, second messenger assays) and high content cellular imaging technologies • Hands on experience in immunological methods e.g. flow cytometry, ELISA, immune cell isolation, antibody characterization •In vivo license and working experience is beneficial, as well as proven experience with complex cellular models, in particular with primary human myogenic cells, and confocal microscopy is advantageous • Highly motivated team player with refined collaboration skills, excellent communication and interpersonal skills Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionNIBRBusiness UnitNEUROSCIENCELocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

05.08.2020

Novartis AG

Novartis Digital (data42) - Are YOU curious?

  • Novartis AG

  • 4040Basel

  • 05.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID284677BRPosition TitleNovartis Digital (data42) - Are YOU curious?Apply to JobSourcing Statement You are applying to be part of the Novartis Talent Pool. We are not currently recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV. Job Description Are you curious? Do you look for an opportunity where YOU can have an impact on people’s lives? Novartis is driving scientific innovation by applying Artificial Intelligence (AI) in pharma R&D to generate new insights and new therapies for patients. Are YOU ready to help re-imagining medicines? We are looking for you! data42 is a key pillar of the Novartis strategy to go big on data and digital. This transformative initiative aims to harness the power of our Research and Development (R&D) data to produce analytics that generate insights about diseases, patient data, and potentially new indications or treatments like never before. Using artificial intelligence (AI) and machine learning, data42 is striving to unlock the full potential of data to enable data scientists to interrogate 2 million years of patient, clinical and research data. We are seeking innovative, curious and agile AI/tech pioneers with business acumen, preferably with experience gained in the pharmaceutical industry and drug development, to help drive & revolutionize the way we develop medicines. Researchers, scientists, data engineers, development & technology leads, agile scrum masters & coaches; we need you. A plus would be experience in digital and strategy. Beyond your knowledge and experience, you will have gravitas, passion and resilience to identify, frame and lead initiatives to embed digital into drug development whilst leading internal/ external partnerships. Novartis can be flexible on location with main digital presence currently located in Basel, Cambridge(US), Dublin and Prague. EEO Statement The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Minimum requirements If You Are... • a Product Owner and Product Manager experienced working with digital products serving Medical and Scientific communities • a Data Scientist and Data Engineer with experience in both omics and clinical data pipeline building plus analysis via machine learning algorithms • a Scientific Lead with experience in clinical trial development and scientific data interpretation (Clinical and Omics) (Knowledge in Immunology, Cardiovascular or Oncology fields a plus) • a User Experience (UX) and Community Engagement Professional experienced working with Medical Scientists ... we are looking for you! Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous, and collaborative people like you are brought together in an inspiring environment, where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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05.08.2020

Novartis AG

Program Manager - Content Journey

  • Novartis AG

  • 4051Basel

  • 05.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID298293BRPosition TitleProgram Manager – Content JourneyApply to Job Job Description Creating a world-class content supply chain, we continually drive unique and relevant customer experiences for millions of Healthcare providers and patients around the world. One of the biggest networks of content studios in the world, with significant investment in internal capability build, translating and trans-creating content to a scale to meet the needs of audiences worldwide, and deliver experiences through more than 1,000 optimized Omni channel campaigns per day! Marketing Content is key to the success of our brands and our ability to realize our mission of improving and extending patients’ lives. The Content Journey Program Manager will lead and direct delivery of large, complex IT projects and programs on time, within budget, with high quality while meeting desired business objectives across the end to end Digital Asset Management (DAM) process. This role will partner with cross functional stakeholders in order to manage the delivery of highly complex global and cross divisional projects. The successful program manager will manage multiple aspects of programs/projects in the areas of business process optimization, technology architecture, support organization structure, and governance structure to be put in place to best manage end to end Digital Asset Management at the enterprise level at Novartis. This would include support for the business processes for Content Creation, Content Referencing, Content Approval, Content Distribution, Content Channel Publishing, and Content Retirement as well as impact to and interfacing with other solutions/platforms as appropriate. Key roles for collaboration and engagement within IT would include the Business Process Expert, Solution Design Manager, Solution Delivery Manager, Domain Architect, and Solution Architect. Come equipped with strong program management expertise and knowledge in the area of Digital Asset Management The program includes investments in fit-for-purpose shared technology that enables efficient delivery of content at scale. Creating an enterprise-wide Medical Legal Review and unified Digital Asset Management platform and processes supported by a global content taxonomy and data model. The processes are enhanced with modular content review/ automation; digital rights management to drive down cost and remain compliant, automation of transcreation aligned to content guidelines for speed and integration of all our digital channels e.g. CRM, web, mobile etc. The objectives and scope includes data democratisation and self-service, ability to measure content process efficiency, content reuse and content performance in channels. Your responsibilities will include: - Direct the delivery of strategic or large programs through active sponsorship, leadership and involvement in specific initiatives to ensure they meet time, cost and quality requirements - Direct outputs of a large project team across divisions and geographical boundaries - Create project plans and initiate program mobilization by confirming scope, estimate, resources, roles and responsibilities - Provide leadership and decision making support by establishing program governance - Monitor and control execution of program though all phases - Ensure overall program success and effective use of resources - Provide program reporting including overall performance of the program and program completion documentation - Drive organizational change - Ensure the overall user experience is taken into account when designing and deploying new solutions and services - Ensure appropriate use of project management methods and tools - Act as mentor in the area of Project Management and influence the personal development of mentees - Take accountability to ensure adherence with Security and Compliance policies and procedures within Program scope Minimum requirements What you’ll bring to the role: - >= 12 years of business and IT experience - Expert knowledge of Project Management methodology, internal IT standards, functional area, technology standards and finance processes. Proven leadership skills with the ability to manage teams. Understanding of organizational change - Business fluent in English (written and spoken) - Knowledge and experience with the pharmaceutical industry and specifically with the commercial / marketing function. Understanding in the area of digital asset management and digital technologies and communication channels deployed to support the marketing function such as websites & portals, social media, email campaigns, marketing automation, CRM, etc. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNBSBusiness UnitIT NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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05.08.2020

Novartis AG

HSE System & Compliance Manager

  • Novartis AG

  • 4040Basel

  • 05.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID298398BRPosition TitleHSE System & Compliance ManagerApply to Job Job Description The HSE System & Compliance Manager will be in charge of the supervision and continuous improvement of the HSE & BC management system of all Swiss R&D and CommOps sites as well as Basel sites functions supported by HSE CH Moreover he will have an overview of the cross-divisional and cross-functional lead of adaption of the HSE & BC management system to the Global HSE requirements and implementation of the Global HSE GOPs. You will be responsible but not limited to: • Ensure alignment among the sites on the global standards and strategic direction related to HSE management system, HSE audits and compliance management • Develop, promote, coordinate and monitor an effective HSE management system for HSE Switzerland and all supported Swiss R&D and CommOps sites • Reporting & data management, supervise timely data entry by regular information on responsibilities and feedback on late or missing data for region Switzerland, conduct periodic monitoring and reporting of the deployment and implementation status across respective sites • Implementation and further development of the HSE process and audit framework to confirm contractor/third party compliance at Basel sites • Oversee management and effective follow-up of audits and conformance reviews lead by Global HSE as well as inspections by authorities incl. management and coordination of corrective and preventive actions (CAPAs) • Manage compliance with national HSE legislations and internal HSE requirements • Ensure compliance disposal of narcotics and precursors with cantonal authorities Minimum requirements • Degree from a university/university of applied sciences in Natural Science, certification as Quality System Manager with respect to Occupational Health & Safety and/or Environment, MAS in Occupational Health, CAS in Integrated Systems & Compliance, certification as External Auditor • Written and spoken German and English, every other language is an advantage • At least 8 years’ experience in the HSE area, industrial experience, preferably in the chemical pharmaceuticals industry, good understanding of the business and operations, auditing and training experience, profound knowledge of HSE management systems • Expertise in the field of HSE Management Systems and auditing Sound knowledge of relevant best practices • Good knowledge of relevant legal and internal HSE regulations WHY CONSIDER NOVARTIS? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis!DivisionNBSBusiness UnitREFS NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaFacilities & AdministrationJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

05.08.2020

Novartis AG

Proteomics - Senior Scientist / Principal Scientist (80-100%)

  • Novartis AG

  • 4040Basel

  • 05.08.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID299407BRPosition TitleProteomics - Senior Scientist / Principal Scientist (80-100%)*Apply to Job Job Description 200+ products in development for nine different disease areas! We are here to serve people affected by diseases, their caregivers and communities. By reimagining medicine, at Novartis we will continue to transform the lives of millions. This is our purpose, driven by a strong sense of curiosity and urgency, which every day inspires and challenges us to never give up. The goal of the NIBR-ASI department is to unleash the power of analytical sciences to enable transformative therapies. For our global proteomics team, we are seeking a highly motivated Senior Scientist / Principal Scientist with profound expertise and broad experience in quantitative LC/MS-based proteomics (analysis of proteins and peptides), and with a passion for solving challenging questions in an interdisciplinary team to enable break-through therapeutic innovations in drug discovery. Depending on your background and experience, this position could be at a Senior Scientist II or at a Principal Scientist I level. What you’ll be doing: You will work in a highly collaborative matrix team environment, developing LC/MS-based proteomics workflows and perform experiments to answer key scientific questions of drug discovery projects. Your responsibilities will include but will not be limited to: • Evaluate and establish quantitative proteomics workflows (diaPASEF, DIA, PRM, TMT) and transfer methods across sites. • Design and execute experiments including sample preparation, LC/MS analysis of proteins and peptides, data interpretation and presentation of results to project partners • Assess and implement new analytical approaches, developed either internally or externally, to further strengthen the group’s technology portfolio • Initiate new project collaborations to answer key scientific questions and advance drug discovery projects with decision-making data. • Mentor junior associates and share experiences broadly throughout the NIBR analytical science network. Minimum requirements What you will bring to the role: • Doctoral degree in systems biology, biochemistry, analytical chemistry or related field OR a Master’s degree with 5+ years of experience in pharma/biotech • Hands-on experience in mass spectrometry instrumentation and proteomics sample preparation workflows (quantitative analysis of proteins and peptides using LC/MS is a must!). • Knowledge of commercial and academic software tools for the analysis of large proteomics data sets as well as basic programming skills (e.g. Python, R). • Demonstrated track record of publications in peer-reviewed scientific journals and ability to translate scientific questions into analytical strategies. • Strong interpersonal communication skills and ability to work in a dynamic working environment with shifting priorities and timelines. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionNIBRBusiness UnitBIOTHERAPEUTIC AND ANALYTICAL TECHNOLOGIES - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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05.08.2020

Novartis AG

Clinical Development Medical Director, Respiratory (80-100% )

  • Novartis AG

  • 4051Basel

  • 05.08.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID299639BRPosition TitleClinical Development Medical Director, Respiratory (80-100%*)Apply to Job Job Description 1st! Novartis is developing the first inhaled biologic treatment for respiratory diseases, with the ambition to transform the lives of patients with asthma and COPD across the globe. As a Clinical Development Medical Director within the Respiratory Franchise, you will oversee the strategy planning, execution, and interpretation of clinical data for a specific indication. Your responsibilities will include but are not limited to: • Acting as a clinical global leader for the assigned indication driving medical strategy implementation and operational deliverables • Providing clinical leadership and strategic guidance for all clinical deliverables in the assigned section of the clinical program • Ensuring effective cross-functional communications to align with global strategy • Leading development of clinical sections of trial and program level regulatory documents • Driving execution of the section of the clinical program in partnership with global line functions • Supporting the clinical research leaders by providing medical input into IDP and CTP reviews and contributing/driving development of disease clinical standards for new disease areas • Acting as the medical expert, engaging with external stakeholders (e.g., regulatory authorities, key opinion leaders, data monitoring committees, advisory boards etc.) and internal Novartis stakeholders Minimum requirements What you’ll bring to the role: • A medical degree is required • Advanced knowledge and clinical training in a medical/scientific area (e.g., respiratory medicine or internal medicine) required, with Medical Board Certification •≥ 5 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV; • Advanced knowledge of assigned therapeutic area • Proven ability to establish strong scientific partnership with key stakeholders • Thorough knowledge of GCP, clinical trial design, statistical analysis methodology, and regulatory/ clinical development process • People management experience preferred, this may include management in a matrix environment. Global people management experience desirable *Some restrictions on flexible working models may apply and will be discussed during interview if applicable Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitCD&A GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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04.08.2020

Novartis AG

Nephrology research Therapeutic Area Head (Associate Director)

  • Novartis AG

  • 4051Basel

  • 04.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID297924BRPosition TitleNephrology research Therapeutic Area Head (Associate Director)Apply to Job Job Description Over 2 million! That’s the number of people worldwide who currently rely on dialysis or kidney transplant to survive. This number may represent less than 10% of the actual number requiring treatment for kidney related illnesses. Novartis is committed to cutting-edge translational research to discover and develop new therapeutics for patients with acute and chronic kidney disease. The Nephrology research group currently explores primary glomerular diseases, gene therapies for monogenic kidney diseases, and new approaches to treat polycystic kidney disease. As the Nephrology Therapeutic Area Head for Disease Area X (DAx), you will contribute to NIBR’s mission to advance the “new science of therapeutics” through innovation in therapeutic target and lead discovery, and enabling clinical progression of new therapeutic opportunities for kidney indications. You will lead a team of interdisciplinary scientists in Basel (Switzerland) and Cambridge MA (USA) tasked with 1. driving innovation and the discovery of novel targets and therapeutic leads in kidney disease 2. preclinical to clinical progression of innovative therapeutic leads in kidney disease 3. coordination of cross-functional, cross-site kidney disease activities and catalyze cross-DA/FA collaboration around translational research, drug discovery, and early clinical development. Your key responsibilities: • Lead a matrixed research group of 11 scientists (3 PhD direct reports who have 8 scientists reporting to them), and indirect reporting scientific collaborators (~30 scientists), to drive innovation in therapeutic target and lead discovery. • Collaborate with Translational Medicine colleagues to define new clinical opportunities in kidney disease and recommends potential drug candidates for evaluation in those new indications • Scientific partner to business development colleagues to evaluate external biotech and academic collaborations, to advance science, drug discovery and translational research • Responsible for portfolio maturation and collaboration with the Portfolio Strategy Director to drive strategic planning, resourcing, and budget management • Coordinate the Nephrology Strategic Working Group, an internal scientific advisory board including Novartis specialists in renal diseases, drug hunting, and clinical development • Member of the DAx leadership team, helping to define the strategic direction of DAx; representing DAx in reviews, internal and external meetings • Responsible for team development and talent management, fostering cross-functional collaborations and synergies to increase team work and time to impact Your Key Performance Indicators will be innovation in target and therapeutic leads; preclinical to clinical progression of novel therapeutic leads, and advance in matrix science Minimum requirements • PhD, or MD with PhD-level research • A completed postdoc and recognized achievements in kidney research including credible publications in international journals • Significant relevant research experience (i.e. 10 years+) and publications after your PhD/postdoc from within biotech/pharma, including experience of line and project managing research scientists and having budget responsibilities. Ideally you have experience of line managing those who themselves are line managers • Advanced project and people Leadership skills and experience, successfully influencing matrix/stakeholder management and teams in an interdisciplinary global environment • Strong capabilities from having defined strategy and effective execution; strong operational, results and change agility • Business-level / Fluent English; German advantageous This position is written for Associate Director. For much stronger applicants, suitable adjustments may be possible for Director. International family relocation is supported. The position will be in Basel or Cambridge: please confirm in your application letter if you wish to be considered for both locations. About Disease Area X (DAx) NIBR's DAx focuses on potentially transformative therapeutics that are outside the remit of other NIBR disease areas and has ~100 scientists and physicians working in Basel and Cambridge MA. The group's current research is on liver diseases, kidney diseases, and non-malignant blood diseases with teams working on each, plus exploratory Translational Profiling for disease characterization, target finding and biomarker discovery; Discovery and Translational Pharmacology developing and running preclinical disease models, and Project and Portfolio Management for team excellence, strategy and governance. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network: https://talentnetwork.novartis.com/networkDivisionNIBRBusiness UnitCBT - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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04.08.2020

Novartis AG

Service Delivery Expert Patient Services

  • Novartis AG

  • 4040Basel

  • 04.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID295213BRPosition TitleService Delivery Expert Patient ServicesApply to Job Job Description 125,000 unique individuals work at Novartis, all with different needs and aspirations, aligned to a single inspirational purpose: to Reimagine Medicine for millions of patients around the world. Come and join the team. Act as the primary point of contact for the Patient Services business - for existing and new services to ensure that agreed services are being delivered to requirements and business user expectations and satisfaction levels are met. Responsible for demand shaping, stakeholder management and oversight on project execution. Point of escalation for business and IT teams, responsible for ensuring project completion to required scope and handover to internal IT support teams as per CIT guidelines. Patient Support Programs at Novartis help enable patient engagement and improve outcomes by helping patients get on-boarded to Novartis therapies in a timely manner. You will have an opportunity to directly affect the patient journey during their treatment and ongoing care. • Act as the primary connection between Service Delivery and the business for a given capability • Ensure IT services are aligned with business strategy, business objectives, business requirements, standards and regulations • Understand the processes, plans, objectives, drivers, and issues related to the business capability, as well as the appropriate external policies and regulations. • Identify and qualify new demand with overall responsibility for steering proposals through the early phases of approval • Participate in establishment of budgets and investment proposals and obtain sponsorship and funding • Ensure the introduction of new / modified services happens in a planned, controlled and timely manner to minimize disruption and maximize benefit • Provide IT consulting to the capability stakeholders, educate them on IT processes and methodologies and drive adoption of global solutions • Ensure service adherence with quality, compliance and security standards and delivery of associated corrective service actions • Provide a uniform approach to the way in which customer feedback is handled and resolved • Ensure technology impact analysis is provided to business • Facilitates project kick-offs contributing to the success of a project team • Take accountability to ensure adherence with Security and Compliance policies and procedures within Service Delivery scope Minimum requirements • 8+ years IT experience with least 3 years’ experience in business facing roles • 6+ years business area exposure (Pharma experience a plus) • Business fluent in English (written and spoken) • Additional languages a plus • Superior customer relationship & consulting skills; Sound knowledge of IT business processes and ability to transform business requirements into consistent and reliable IT solutions, processes and services • Demonstrated strategic thinking and application of product/portfolio roadmaps • Expert understanding of digital solutions / technology for patient services area preferableDivisionNBSBusiness UnitIT NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

04.08.2020

Novartis AG

Lab Head, Immune Nephrology - Principal Scientist (80-100% )

  • Novartis AG

  • 4040Basel

  • 04.08.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID289457BRPosition TitleLab Head, Immune Nephrology - Principal Scientist (80-100%*)Apply to Job Job Description 105,000! The number of unique individuals that work at Novartis, all with different needs and aspirations, aligned to a single inspirational purpose: to Reimagine Medicine for millions of patients around the world! The department for Autoimmunity, Transplantation and Inflammation (ATI) within the Novartis Institutes for Biomedical Research is investigating the discovery of innovative and transformative therapies to improve the lives of patients suffering from autoimmune and inflammatory diseases. We are currently seeking an experienced and highly motivated individual to initiate and guide research and drug discovery projects in the area of immune nephrology. Your responsibilities will include but are not limited to: • Lead a state-of-the-art laboratory of BSc/MSc level scientists to discover and develop novel therapies for vascular and autoimmune renal diseases • Contribute to and/or lead early drug discovery projects within multidisciplinary teams up to clinical proof-of-concept studies in patients • Define and execute on innovative scientific strategies, test novel hypotheses and develop transformative therapies • Closely collaborate with scientists, clinicians, and technology experts across different departments in the global organization • Contribute scientific findings resulting in impactful publications in peer-reviewed journals Minimum requirements What you’ll bring to the role: • A PhD degree with several years of postdoctoral experience with a strong background in immunology combined with nephrology, vascular inflammation or renal autoimmunity. Areas of interest include (i) autoantibody-driven renal diseases, (ii) end stage renal disease associated inflammatory and vascular changes, (iii) sepsis associated acute kidney injury • Significant scientific accomplishments and successful collaborations documented by publications in high-impact journals • Strong technical and theoretical background/expertise in immunology and vascular biology • Proven track record of leadership, strategic thinking, creativity, and risk taking • Excellent communication, presentation and analytical skills Desirable requirements: • Experience as an independent research scientist in an academic setting and/or in the pharmaceutical/biotech sector • Proven success in independently initiating and leading projects Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionNIBRBusiness UnitAUTO/TRANS/INFL - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.08.2020

Novartis AG

Bioinformatics Software Engineer

  • Novartis AG

  • 4051Basel

  • 03.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID297150BRPosition TitleBioinformatics Software EngineerApply to Job Job Description 71…We have 71 drugs in the Novartis Global Pipeline for Oncology, these are 71 new potentially life-saving treatments for cancer patients. We are seeking a software engineer to contribute to applications for data processing, harmonization and visualization. Your work will be challenging, impactful, and relevant to the core mission of NIBR Oncology, and will directly accelerate research which brings new, life-saving products to the clinic. The Oncology Data Science (OncDS) group in NIBR Oncology seeks to advance biological understanding and improve the lives of patients with cancer. The group generates sequencing data from thousands of oncology clinical samples, which are analyzed with internal bioinformatics pipelines. Your projects will focus on preclinical and clinical applications including marshalling, transforming, and integrating internal and publicly available data to facilitate the generation of new scientific hypotheses. These tools will leverage a wide range of existing services and require strong collaboration with associates across the group to understand and improve our services. You will work in a dynamic multi-cultural environment, where we are keen to embrace new ideas and technologies to deliver innovative solutions for our emerging challenges in data science. You will be joining a tightly-knit global software engineering team located in two different locations and time zones. You will be responsible but not limited to: • Write clean code, employing good software engineering principles, e.g. SOLID. • Use modern tools such as Jira, Confluence, Jenkins, and Bitbucket to implement best practices in documentation, TDD, CI / CD, code review, and iterative development. • Actively participate in an agile environment to efficiently produce high quality software, to contribute to meetings, and to achieve team goals. Minimum requirements • Education: B.S., M.S., or equivalent experience in computer science. • 1-3 years experience would be ideal • Knowledge and experience of software development. • Knowledge and experience of biological sciences or desire to learn about genetics & genomics. • Fluency in English as a business language. • Good software development programming skills in Java 12+, JavaScript, and Python 3+. • Experience with front-end and back-end technologies, e.g. Spring 5, React 16 and FastAPI. WHY CONSIDER NOVARTIS? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis!DivisionNIBRBusiness UnitOncology NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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03.08.2020

Novartis AG

Service Operations Expert - Finance & Procurement Analytics

  • Novartis AG

  • 4040Basel

  • 03.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID297308BRPosition TitleService Operations Expert - Finance & Procurement AnalyticsApply to Job Job Description 60! That is the size of applications portfolio utilized for Finance & Procurement analytics. Purpose of the position is to contribute to the day-to-day management of a set of systems, tools or applications in the Finance and Procurement area, ensuring their stability and integrity, while meeting customer service levels. This role is specific to Crown Jewels, SOX and SOCA (Security & Operationally Critical applications) delivering critical Services to CH based and Global Finance and Procurement Business areas. Your key responsibilities: Your responsibilities include, but are not limited to: • Supervise the delivery of an assigned portfolio of applications and ensure their stability, integrity and business continuity. • Ensure services are delivered to the agreed SLA, periodically reviewing supplier performance based on the agreed SLAs and critical metrics • Handle customer critical issues and communications for BI community in responsible area. • Ensure reduction/containment of high impact incidents. • Address problems by driving identification of root causes and prevention of recurrences in collaboration with vendor command centers. • Ensure that an up-to-date asset inventory is maintained and only authorized components are used; coordinate configuration management database changes and/or ensure that configuration items are identified, accounted, reported, verified and audited. • Ensure accurate user and access management and regular user access review procedures are followed. • Ensure alignment to detailed operational procedures and quality standards, and that appropriate operational service documentation is built and accepted by partners. • Collaborates with the rest of IT functions to ensure quality services are seamlessly delivered to the business partners as per agreed own and other IT Units service descriptions • Maintain and ensure all application data are consistent across repositories. • Provide improvement suggestions and follow them to the closure • Take accountability to ensure alignment with Security and Compliance policies and procedures for the applications in scope. Minimum requirements What you’ll bring to the role: • Bachelor’s degree in computer Science or equivalent education/experience. • Total 8+ years’ IT experience 5+ years BI experience, validated skills & experience in Service management and/or business analyst and consulting. • Experience in working in an operational BI and Analytics environment • Good level of expertise in BI and Analytics Technologies • Prior experience and functional knowledge in the areas of Finance and Procurement preferred. • Solid grasp of IT service management processes and experience in improving processes. Preferably, ITIL Intermediate certified. • Good communication and partner engagement skills • Experience in working and collaborating with global multi-functional teams and managing relationships with business customers • Experienced in vendor management and working with 3rd parties onshore & offshore. • Ability to work efficient and collaboratively in a complex matrix organization •Ability to understand and influence partners within and across the function, building trust and change agenda demonstrating both the formal and the informal elements of the organization Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Novartis are an equal opportunities employer and welcome applications from all suitably qualified persons.DivisionNBSBusiness UnitIT NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.08.2020

Novartis AG

Lab Head, In vivo Pharmacology & Molecular Imaging (80-100% )

  • Novartis AG

  • 4040Basel

  • 03.08.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID294506BRPosition TitleLab Head, In vivo Pharmacology & Molecular Imaging (80-100%*)Apply to Job Job Description 6500! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. The Laboratory Head position in Oncology Research that will carry out cutting-edge research in the areas of in vivo pharmacology and molecular imaging together with leading basic research groups within NIBR. The candidate will be responsible for leading a team of pharmacology associates performing drug discovery pharmacology activities within oncology biologics, small molecule and other therapeutic modalities. We seek an experienced, motivated and ambitious scientist wishing to continue a successful scientific career in a fast-paced drug discovery environment. The position is based at the Novartis Institutes of BioMedical Research in Basel, Switzerland. The ideal candidate should have a proven ability to conduct multidisciplinary research in a competitive field and an excellent record of achievements and a strong scientific and industry background with expert knowledge in performing all aspects of pre-clinical pharmacology in rodents from target identification to early clinical development. Hands-on experience in various in-life molecular imaging techniques including uCT, ultrasound and flourescent imaging is required. The successful candidate will have solid expertise with rodent in vivo cancer models and is expected to play a key role in the establishment of novel rodent models in the field of cancer. Responsibilities will include but are not limited to: • Lead a pharmacology laboratory with expertise in innovative imaging modalities • Perform efficacy studies with associated PK/PD read-outs and metabolites analysis ex vivo • Engage in independent research that will lead to innovative findings and novel fundamental insights within the portfolio • Lead and manage cross-functional projects and external collaborations. Drive the project decision-making process, conceptualize and drive research projects to completion Minimum requirements What you’ll bring to the role: • Ph.D. in pharmacology, bioengineering, biotechnology or related field • At least 5 years of industry-relevant experience in drug discovery • Meticulous, independent and self-motivated personality with a drive to learn new techniques, expand knowledge and take on responsibilities • The position requires excellent communication skills in English and the motivation to work independently within a global team Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionNIBRBusiness UnitOncology NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.08.2020

Novartis AG

Senior Legal Counsel NTO Transactions

  • Novartis AG

  • 4040Basel

  • 03.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID298724BRPosition TitleSenior Legal Counsel NTO TransactionsApply to Job Job Description 70+ billion! That’s the number of units Novartis Technical Operations (NTO) supplied to over 150 countries in 2019. Our 26,000+ associates from 100 different countries are working hard to build an inspired, curious and unbossed culture in which everyone is enabled to be their best. We are unleashing the power of our people and putting data and digital at the heart of a transformation that is enabling us to reach more patients, more quickly, all across the world. To support the Novartis aspiration of becoming the leading medicines company in the world, we are reimagining manufacturing, aligning our capacity and capabilities with the changing needs of the Novartis portfolio. As our evolution continues, we are proud to provide the manufacturing technology on which many of our innovative new treatments rely and to be the organization that provides our patients with the medicines they need to live longer, healthier lives. As our Senior Legal Counsel NTO Transactions, you will support the Head Legal NTO Transactions in any strategic projects and act as lead lawyer for NTO in assigned global transactions / projects in the area of Network Transformation, M&A and BD&L; ensure strategic legal advice, robust risk assessment, and effective and efficient legal support during all stages of the relevant transactions / projects, in accordance with NTO strategy, and in compliance with all relevant laws and regulations Your responsibilities will include: • Acts as a pro-active, business-minded legal partner to the Network Transformation, M&A and/or BD&L NTO global support teams during planning, negotiation, execution and implementation of the relevant transactions / projects, and ensures the execution of projects in accordance with the project plan, NTO strategy and in compliance with all relevant laws and regulations. • Represents NTO Legal as lead lawyer in all assigned projects in the area of Network Transformation, M&A and/or BD&L, and, as required, prepares / conducts due diligences, drafts, negotiates and reviews all related agreements, and any related internal or external communication to management, employees, authorities, interested parties, suppliers or any other third party. • Is an acknowledged expert resource for the entire NTO function in their field, and plays a key coordination role for all relevant legal and other functional experts’ input to any transaction or implementation documentation. • Manages and works with outside counsel and, when and as necessary, closely monitors and controls related legal spend. • Manages potential disputes and dispute resolution relating to the assigned transactions / projects. • Supports the establishment, design and implementation of clear guidelines and processes to provide optimal and timely NTO legal support for transactions / projects, while ensuring their execution and implementation in accordance with NTO strategy and in compliance with all relevant laws and regulations. • Advises and determines appropriate actions regarding legal and compliance issues in relation to transactions / projects, including the training of lawyers and clients Minimum requirements What you’ll bring to the role: • Experience representing the organization Law School Graduate & Bar member. Additional qualifications in related fields (e.g. finance, tax, regulatory, etc.) are a plus. • Acknowledged as an expert and a resource for the legal function in the manufacturing, regulatory and transactional field with the ability to: analyze complex legal issues; lead contract negotiations of several complex projects independently; and play a key coordination role with lawyers and other functional experts, with a minimum of: • 8 years post-Bar experience, ideally gained within an healthcare / pharmaceutical environment or, alternatively, with a top-tier law firm representing healthcare clients, of which 5 years of that experience in leading complex legal transactions, restructuring and outsourcing projects. • Able to set priorities and to manage a wide-ranging workload under time and organizational pressure, often involving multiple projects simultaneously. • Excellent team player with strong verbal and written communication Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionNovartis Technical OperationsBusiness UnitNTO LEGALLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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03.08.2020

Novartis AG

Internship Support Services for Live Magazine

  • Novartis AG

  • 4051Basel

  • 03.08.2020

  • Praktikumsstelle

Back to Previous Page Job ID299907BRPosition TitleInternship Support Services for Live MagazineApply to Job Job Description The Live Magazine is the external story-telling platform of Novartis. The media-rich platform highlights some of the biggest breakthroughs at Novartis. Supporting the platform to maintain its high-quality output helps Novartis build trust and reputation with third party and internal stakeholders. Your responsibilities: Your responsibilities include, but are not limited to: • Support the live magazine team, preparing copy for the online version, including writing and editing abstracts • Collecting model releases and building an online residue for legal checks • Help preparing the publication for social media assets, i.e. collecting pictures for digital promotion Minimum requirements What you’ll bring to the role: • Current Master student in Communications, digital Communications, Media, Social media, Journalism or similar is a must • Fluent English (written & spoken), additional language is a plus • Very good knowledge in editing an writing • First internship experience in a similar role preferred Timing: as soon as possible Duration: Until December 31, 2020 Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionCORPORATEBusiness UnitCorporate CommunicationsLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.08.2020

Novartis AG

Master Student

  • Novartis AG

  • 4040Basel

  • 03.08.2020

  • Praktikumsstelle

Back to Previous Page Job ID292093BRPosition TitleMaster StudentApply to Job Job Description 6000! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. We are looking for a highly motivated and committed student to join our protein structure and biophysics research team in Basel. This internship position requires application of bioNMR techniques for characterisation of protein-ligand and protein-protein complexes in combination with other biophysical methods to drive drug discovery projects, especially at early stages of pharmacological target validation, hit generation, hit to lead optimisation and drug candidate discovery. Minimum requirements • University or TH student in biochemistry, chemistry or life sciences, with or without bachelor’s degree. • Practical experience in biochemistry and biophysics is essential. Skills in protein purification, protein crystallisation, biophysical or biochemical techniques would be advantageous. • Experience with NMR is considered a significant advantage, although training will be provided in the job. • Open communication, and an independent and precise way of working are important. • Ability to work in a team and interact with colleagues in a multicultural environment. • Good knowledge of spoken and written English is required. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionNIBRBusiness UnitCBT - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

02.08.2020

Novartis AG

Principal IP Counsel-Head European Patent Oppositions

  • Novartis AG

  • 4040Basel

  • 02.08.2020

  • Vollzeitstelle

Back to Previous Page Job ID296329BRPosition TitlePrincipal IP Counsel-Head European Patent OppositionsApply to Job Job Description 300! That’s the number of active European patent oppositions pending at the Novartis Group, with more than 50 added each year. The Head of EP Oppositions will lead our cross-functional working group and interact with our excellent European patent attorneys in their divisions to ensure that every opposition is best positioned for success. Manage Novartis Group approach to European Patent Office oppositions, including superior knowledge and use of EPO best practices for success in defensive and offensive oppositions, training and coaching in-house attorneys, as well as law firm management; participate in litigation review processes as a highly contributing member of Group IP Litigation team. Your responsibilities will include: • Lead functional group-wide EP opposition team, collaborating with divisional opposition team members and colleagues to develop best-in-class strategies, cross-divisional alignment, and substantive arguments for key oppositions. • Provide initial and on-going strategy review of EP oppositions with Divisional IP litigation teams, as well as second opinion on key EP opposition strategy and arguments, also in due diligence situations; operational or day-to-day management of some EP oppositions. • Lead development of and/or develop critical trainings, mock hearings, and workshops for Legal and IP stakeholders regarding EP oppositions (including litigators and patent prosecutors), and coach and mentor internal European Patent Attorneys in preparing and arguing oppositions, and monitor and audit of overall opposition performance. • Develop and manage top tier external counsel support for all oppositions, including selection of counsel, budgeting, and performance assessment. • Interface with IP leaders and team members for US IPRs/PGRs and opposition-style proceedings in other jurisdictions, to coordinate for consistency across proceedings and to share key learnings. • Participate in Group Litigation Review processes, including review and comment on divisional litigation proposals and related external opinions. • Work with IP leadership (including Global Head IP Litigation, Global Head IP Policy, and Global Head IP Strategy) on special projects, including preparation of IP papers, positions, and comments to new policy and other IP initiatives. • Member of Group IP and Global Litigation teams. • Advocate internally and externally for NVS positions, including relationship building with EPO; support other Group functions as needed and directed. Minimum requirements What you’ll bring to the role: • EQE, and national patent attorney qualification or legal equivalent; • Scientific degree BA, BSc, Masters, or PhD in a science relevant to biopharmaceutical patent practice Fluency in English • At least 12 years post-bar/EQE experience required, including at least 10 years of active participation in and argument of European Patent oppositions • Significant exposure to and participation in litigation proceedings outside of the European Patent Office, preferably in European countries and the United States • Demonstrated writing abilities and oral advocacy experience Optional: Law school graduate and qualified attorney-at-law (Bar member) in common law jurisdiction, with legal doctorate (J.D. or equivalent). Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionCORPORATEBusiness UnitGROUP LEGALLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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02.08.2020

Novartis AG

Senior Pharmacovigilance Process Manager (80-100% )

  • Novartis AG

  • 4051Basel

  • 02.08.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID297161BRPosition TitleSenior Pharmacovigilance Process Manager (80-100%*)Apply to Job Job Description 250! As Senior PV Process Manager, you will improve the daily work of 250 Novartis associates by ensuring a smooth and efficient process for preparation of aggregate reports. You will develop, monitor and optimize pharmacovigilance processes and associated metrics for preparation of aggregate reports to drive performance and quality, and ensure compliance with the worldwide regulatory requirements. In this role, you will act as the functional lead and process owner for aggregate reporting processes (DSUR, PSUR, US Periodic Reports, or similar) within a diverse and globally distributed team of 6 – 7 process managers. Your responsibilities will include: • Lead the development and maintenance of procedural documents • Drive continuous process optimization and simplification, develop training and communication strategies • Ensure ongoing compliance to global regulatory requirements • Establish clear processes for tracking regulatory compliance as well as compliance to internal requirements; work jointly with other Novartis functions to perform metrics trend analyses, generate knowledge and mitigate any identified risks. • In case of incompliance to process or regulations, ensure investigation into the root cause and implementation of corrective and preventative actions is performed and the effectiveness of the actions measured. • Support Pharmacovigilance Process Excellence management with developing and implementing objectives and group operational strategy • Acting as subject matter expert during audits and inspections; lead the preparation of responses to findings and the development and implementation of CAPAs Minimum requirements What you’ll bring to the role: • PharmD, MSc degree or equivalent in life sciences or related subject • Fluency in English (written and oral) • Minimum 7 years of experience in the pharmaceutical industry, particularly pharmacovigilance and aggregate reporting (DSUR, PSUR, US Periodic Reports or similar) • Proven organizational and project management skills with the ability to lead global and cross-functional working groups; dealing and interacting with a wide variety of people at all levels • Strong negotiation and communication skills • Experience of working with and supporting a team; ability to coach and mentor Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitCMO & PATIENT SAFETY GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

31.07.2020

Novartis AG

Global Franchise Public Affairs Lead IHD

  • Novartis AG

  • 4040Basel

  • 31.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID297996BRPosition TitleGlobal Franchise Public Affairs Lead IHDApply to Job Job Description 5! Our portfolio of innovative IHD medicines either in the late stage pipeline or already available to patients. The Global Public Affairs lead for the IHD franchise is a business critical role focused on building trust with society and shaping the environment to help ensure our innovative medicines reach the patients who need them. The Global Public Affairs lead for the IHD franchise is a business critical role focused on building trust with society and shaping the environment to help ensure our innovate medicines reach the patients who need them. With a deep knowledge of the pharmaceutical business model, healthcare systems and political and economic environment in the respective area, you will pro-actively lead the -shaping of the Health Care policy environment across the respective area to ensure sustained access to innovation. You will position Novartis as a trusted partner and policy thought leader -building strong stakeholder relationships and partnerships -as well a strong, effective Public Affairs team across the assigned area, supporting all divisions -delivering political intelligence and advice to all Novartis businesses. •Identify and communicate on key political developments affecting Novartis •Shape public policy and legislation by: prioritization of policy trends/issues in alignment with respective area; •Provide leadership for the development of Novartis positions on key issues and strategic country plans •Execution of the advocacy strategy where applicable and ensure Novartis leadership in key trade associations •Identify and manage key business issues with a political component for assigned area •Design and execute product advocacy where applicable -Functional leadership by managing talent for the assigned area •Guide management and the team in political analysis of external trends and development •Shape and protect sustainable healthcare systems policies (pricing, value & access, regulatory, use of data) to support the Novartis IHD portfolio Partner with the business to prepare favorable market conditions for pioneering treatments with a particular focus on pre-launch support •Ensure economic policies conducive to the Novartis business •Equip internal organization with timely policy issue updates, messaging and capability building Co-create access solutions and HCS shaping/ strengthening with business Minimum requirements • Master degree in Health Policy, Political Science, International Affairs or related; MBA or PhD a plus • Fluency in English; • 10+ years working in global health, program implementation, program design and/or policy, ideally with some field experience; • Preferably 5+ years in industry • Proven ability to work with diverse groups of stakeholders, from high level policy makers to community-based groups • Excellent written, oral communication skills and ability to persuade and influence without power • Excellent organizational management experience operating in an ever-changing environment Why consider Novartis? 817 million. That’s how many lives our products touched in 2018. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionCORPORATEBusiness UnitNOVARTIS CORPORATE AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaCommunications & Public AffairsJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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31.07.2020

Novartis AG

Head of IT Scientific Products, Information Products and Data Sciences

  • Novartis AG

  • 4051Basel

  • 31.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID284546BRPosition TitleHead of IT Scientific Products, Information Products and Data SciencesApply to Job Job Description 6,000 scientists and physicians around the world use our data to reimagine medicine and create therapies that save lives. Our research is focused on discovering innovative new drugs that will change the practice of medicine. Novartis Institutes for BioMedical (NIBR) is the global pharmaceutical research organization of Novartis with a mission to discover innovative medicines that treat disease and human health. To do that, our scientists need cutting-edge, state-of-the-art computing systems and NIBR Informatics (NX) is a strategic investment into informatics capabilities, positioning to deliver the systems and services are critical to the future of drug discovery. The Information Products and Data Sciences (IPDS) group in NX is driven to maximize the impact and value to NIBR of software and data. We deliver powerful, functional, beautiful, and integrated software solutions that create a frictionless user experience. Our organization is here to build and apply excellence in product and data management to further Novartis drug discovery. ---- Novartis Institutes for BioMedical (NIBR) is the global pharmaceutical research organization of Novartis with a mission to discover innovative medicines that treat disease and human health. Our scientists need cutting-edge, state-of-the-art computing systems and NIBR Informatics (NX) is a strategic investment into informatics capabilities and positioning to deliver systems and services that are critical to the future of drug discovery. NX is a global team of ~350 technology scientists and business professionals working across 5 sites, primarily Cambridge MA (USA) and Basel (Switzerland). - Interview with NIBR CIO: https://www.novartis.com/stories/people-and-culture/qa-new-nibr-cio-dimitris-agrafiotis ---- Job Description: As the Head of Scientific Products, you will develop and continually update a vision for the suite of scientific products that support NIBR drug discovery and lead the product management team to the successful realization of that vision. Your vision will inspire the cross-functional product organization to deliver value to our scientists and will sustain our team through challenging times. You will bring together technologies, capabilities and outstanding talent to create products that our users will love. You will define the standard for excellence in product management in our organization and synthesize that with your knowledge of drug discovery to create scientific software that enhances and helps drive NIBR science. The Head of Scientific Products will prioritize product roadmaps, direct development resources to maximize value to NIBR science, and will define how we measure product success and value delivery. You will be responsible for identifying opportunities that lead to the growth of our products through constant improvement and innovation while also providing consistent delivery and stable operation of products. You will use your knowledge of these products to promote their meaningful use by giving product demos, sharing user stories, and showing the connection of our scientific products to drug discovery impact. You will work closely with colleagues in engineering, user research, design, support, training, and data science to empower matrixed product teams that deliver on your vision for our products. This will require you to align and coordinate with other departmental leaders and stakeholders to ensure all operational needs are met including security, stability, usability, and sustainability. Responsibilities include but are not limited to: •Lead, manage and mentor a team of product managers. •Product lifecycle management from concept to launch of the products across all scientific product lines. •Lead, define, represent and communicate product portfolio strategy to all stakeholders and NIBR leadership. •Assess product development progress and enhancement opportunities. •Evaluate product development results. •Evaluate and provide input into strategic plans for each product line. •Drive innovative ideas, solutions and products through leadership and decisive action. •Build incredible teams and processes to deliver products that satisfy the needs of customers. •Become the key evangelist of our products and participate in education activities, conferences, discussions with thought leaders within and outside of Novartis. •Regularly present to stakeholders, NX, and NIBR leadership Minimum requirements What you will bring to this role: •Bachelor, Master or PhD in biology, chemistry, computational biology or computational chemistry (PhD preferred) •Minimum of 10 years of experience in IT product management in complex matrix environments •Five or more years of work experience in a drug discovery environment or a core supporting scientific discipline such as biology, chemistry, or computational sciences •Expertise on the Product Team Model and Agile software development •Strong quantitative skills and the ability to use data and metrics to inform decisions Additional required core skills: •Outstanding interpersonal and communication skills; adept at working with colleagues from diverse disciplines and at all levels of the company. •Proven experience in team building, mentoring, and leadership •Demonstrated strength as a team player •Strong leadership skills with a proven ability to win others to follow a common vision •A clear and visible set values and demonstrated integrity •Proven ability to execute consistently, rapidly, and effectively •Self-motivated •Calm under pressure •Ability to travel 25% Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network: https://talentnetwork.novartis.com/networkDivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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31.07.2020

Novartis AG

Scientific Communication Director Ophthalmology (80-100% )

  • Novartis AG

  • 4051Basel

  • 31.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID296092BRPosition TitleScientific Communication Director Ophthalmology (80-100%*)Apply to Job Job Description 1.5 million! The number of Health Care Professionals that can be reached by just 3 journal publications, led by the scientific communications associates at Novartis. As part of a team driving innovation and excellence in scientific communication and engagement, this is an opportunity to anticipate the future, provide strategic expertise for evidence dissemination and scientific differentiation of our medicines, and deliver operational excellence. Your responsibilities include, but are not limited to: • Lead and drive Scientific Engagement & Communications (publications, scientific events, medical education and stakeholder engagement) strategy for an assigned brand(s), working closely with the cross-functional team • Ensure the execution of strategic scientific communication plans, including KPI setting and measurement • In collaboration with the Medical Affairs team, ensure scientific communications launch readiness as part of early medical launch leadership • Functional line management of Scientific Communications Associate Directors • Lead Medical Society Engagement within the Franchise or assigned disease area with specific focus on medical education and congress collaboration • Be the subject matter expert for scientific communications within the therapy area Minimum requirements What you’ll bring to the role: • An advanced degree in life sciences/healthcare (or clinically-relevant degree). PharmD, PhD desirable. Fluent English (oral and written) • More than 10 years in pharmaceutical or healthcare companies including experience in countries and/or Global organization (departments with focus in Medical Affairs, drug development or marketing) • Experience and proven success in the development of medical affairs or scientific communication strategies in pharmaceutical/healthcare companies, including leveraging of new technologies and digital solutions and strong project management skills • More than 5 years of demonstrated leadership including management in a matrix environment, across functions, regions and countries, with the ability to influence, engage and problem solve • A thorough understanding of internal/external ethical guidelines relevant to the pharmaceutical industry. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionPHARMABusiness UnitGLOBAL MEDICAL AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

31.07.2020

Novartis AG

Medical Director, Dermatology Translational Medicine

  • Novartis AG

  • 4051Basel

  • 31.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID299943BRPosition TitleMedical Director, Dermatology Translational MedicineApply to Job Job Description 350 million! That is the estimated number of patients worldwide suffering of atopic dermatitis or psoriasis. Join Novartis to help find the right drugs to transform and improve patient's lives all around the world. You will provide medical and scientific leadership and expertise in a role that significantly impacts the entire Novartis Dermatology drug development pipeline. • Drive success of early global programs, develop and implement strategies to achieve clinical Proof of Concept • Drive success of late global programs when appropriate by developing and implementing strategies that lead to clinical pharmacology, design of mechanistic studies and profiling packages that meet regulatory requirements and support differentiated and competitive drug labeling • Provide scientific expert assessments and support for in-licensing opportunities, including due diligences Your responsibilities: 1. Translational Medicine / early clinical projects: In collaboration with your Translational Medicine Therapeutic Area Head or other Translational Medicine Experts, develop high value decision-strategies for the Translational Medicine component of drug development projects from Research to clinical Proof of Concept or Proof of Mechanism in a single or multiple indications, including Parallel Indication Expansion-Proof of Concepts • Represent TM and lead global project teams through First in Human and Proof of Concept phase to drive implementation of the Proof of Concept strategy • Convene relevant internal and external leaders together to consider the proposed approach to Proof of Concept • In collaboration with research contribute to the proposal of new targets or indications for existing compounds • Responsible for clinical portions of the Integrated Development Plan, including the Clinical Development Plan and Clinical Pharmacology Plan • In collaboration with research scientists, identify, develop, and implement strategy for preclinical support of clinical program-related scientific objectives. This includes assessment of medical need, proposal of clinical development pathways, and review of preclinical data for clinical implications, and other relevant activities 2. Accountable for compound and disease related biomarker strategies, working closely with Biomarker Experts in implementation 3. Develop and implement study protocols for different types of clinical studies (First in Human, Proof of Concept, mechanistic and safety studies), and other documents such as investigators brochures. 4. Responsible for clinical monitoring and integrated safety data review during and after the live phase of a study 5. Provide medical and scientific leadership and expertise to all line functions on the study team 6. Leadership • Lead study-specific teams/ clinical trial teams • Represent TM or lead NIBR project teams • Lead NIBR-sub-teams on Global Project Teams for late-phase programs • Represent Translational Medicine on global development teams 7. Represent clinical Translational Medicine aspects to Health Authorities and other stakeholders (e.g. payers, patient advocacy groups) 8. Represent clinical Translational Medicine in reviews of external opportunities 9. Oversee publication and external presentation of study results 10. Innovation: Champion and drive new clinical compound characterization opportunities and profiling approaches 11. Contribute to initiatives that drive innovation, quality, and efficiency across Translational Medicine 2. Translational Medicine (late-stage clinical projects): In collaboration with your Translational Medicine Therapeutic Area Head: • Responsible for implementing studies during the Proof of Concept phase by providing medical and scientific leadership and expertise to all line functions on the project team. This may include methodology studies to identify and validate novel endpoints for early decision making in Proof of Concept studies. • Drive analysis of studies and present results to relevant decision boards • Communicate clinical team matters to Global Project Teams, relevant Novartis Institutes of BioMedical Research and Global Drug Development boards, and other Novartis Boards as required. • Evaluate clinical centers and foster communication with crucial collaborating investigators, regulatory authorities, and other stakeholders • Provide support for dose selection, design and other clinical pharmacology matters throughout the development cycle • Responsible for content and authoring of documents needed for submission documents with Translational Medicine input (CO, SCE, SCS, SCP, SBP) of NDAs, sNDAs, MAAs, BLAs from regulatory submission through drug registration, including advisory committee and scientific advice group meetings Key Performance Indicators: • Delivery of proposed Development Candidate and Proof of Concept Plan Approval milestones, and Proof of Concept results, according to timelines • Team leadership skills that create high performing teams and drive efficient conduct of innovative, interpretable clinical results • Strong adherence to and modeling of Novartis values and behaviors • Quality of contribution to disease area strategy discussions and contribution to Clinical Pharmacology plans / Profiling strategy discussions and external collaborations Matrix people responsibility per project: 5-8 cross-functional members from within Translational Medicine plus other line functions per project team Impact of this role? • Design and implementation of early Clinical Development Plan and studies according to the Integrated Development Plan / Clinical Development Plan / Clinical Pharmacology Plan enabling efficient and rational decision-making, high probability of fast drug registration, favorable drug label and high competitiveness of compounds • This role has a key impact on the entire Novartis pipeline, transitioning programs from preclinical through early clinical and ultimately to full development via the Proof of Concept mechanism, and driving the program after Proof of Concept by delivering key Profiling data to support regulatory submissions • Recognized Expert in field, drives project team clinical strategy. Works globally across various Novartis Institutes and Divisions as well as country organizations as appropriate Minimum requirements What you’ll bring to the role: • Medical Degree and additional PhD/post-doctoral equivalent immunology research • Specialized further training (board certification) and / or clinical research experience in dermatology / immunology preferred • Advanced / business-level / fluent English (oral and written) • Recognized for medical expertise: demonstrated excellence and clinical / patient expertise in dermatology / immunology • Recognized for scientific expertise: respected by colleagues internally and externally, you’ve made significant contributions to your field and created / established new concepts; record of high quality publications in international scientific journals. • Previous relevant & significant clinical study experience: either from pharma/biotech leading early phase clinical trials; a senior role within a CRO responsible for leading the medical relationship with Sponsors; from a relevant academic medical center with PI & co-PI clinical trial experience. You are used to working independently and within teams including scientists and non-scientists on study planning and execution, demonstrating competence in a broad range of project and more strategic planning skills • Excellent written and oral communication/presentation skills, used to distilling and effectively conveying significant messages to different audiences Your behavioral characteristics • Demonstrated passion for treating patients and science • Strategic thinker: you have created major innovations, networked with and influenced external medical leaders with your clear and logical presentation of complex strategic issues • Innovation: a curious mind and a natural instinct to seek out new clinical discovery opportunities and clinical study approaches • Results-driven self-starter and decision taker; good planning, prioritization, problem solving and organizational skills; strong cooperative team player, flexible in a changing environment; Resilient, energetic and enthusiastic; responding constructively to challenging new ideas and input This position is written for Director - we can hire Executive Director for those with significant Pharma careers, or Associate Director if you have limited clinical study experience or a less established scientific record but have already demonstrated impactful new thinking and innovative clinical & scientific approaches within your career. ABOUT TRANSLATIONAL MEDICINE: Translational Medicine is a global group of scientists and Physicians working at the pre-clinical and early clinical stage of drug discovery. Our Physician-Scientist Discovery & Profiling group drives innovative and cutting–edge science from Discovery to the market through the selection, profiling and effective global development of successful medicines. The group closes the gap between preclinical research and clinical development and integrates clinical science into the discovery and preclinical development phase. Our Translational Medicine concepts are driven by medical needs of the patient and the concept of personalized medicine, tailoring the drug, its dose and dosing regimen in such way to the patient that the clinical response is optimal in terms of efficacy and safety. We focus from identification of drug targets (molecular pathways relevant to disease) up to the completion of Proof of Concept (Phase IIa studies). Our Translational Medicine Experts are part of preclinical project teams in all drug discovery phases and help design the pathway for First in Human studies (healthy volunteer) that bridge to studies in the patient population. They have the comprehensive responsibility for designing and executing the early clinical drug development phase together with a project team from researcher, biomarkers, biostatistics, modeling and simulation, toxicology, technical experts and the clinical trial teams.DivisionNIBRBusiness UnitTranslational MedicineLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

29.07.2020

Novartis AG

Multi-Therapeutic Area Head / Biomarker Strategy Lead (Director)

  • Novartis AG

  • 4051Basel

  • 29.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID294317BRPosition TitleMulti-Therapeutic Area Head / Biomarker Strategy Lead (Director)Apply to Job Job Description 800 plus biomarker discovery and development projects, across more than 100 clinical studies, which generate 20 petabytes of patient data! All waiting for you to unlock the next breakthrough in medicine. Biomarkers are critical components of translational research, enabling robust therapeutic and mechanistic hypothesis testing in early clinical development, and as precision medicine enablers e.g. defining patient subpopulations, predicting patient responses, and use as diagnostics. As a Therapeutic Area Head (TAH) in NIBR Biomarker Development (BMD) leadership, your responsibilities will include: • Representing Biomarker Development on Hepatology, Renal, Hematology and Tropical Diseases Disease Area Decision Boards to identify, develop, and drive disease and mechanistic biology, translational pharmacology and precision medicine approaches for the portfolio • Leading a dedicated matrixed group of biomarker subject matter experts and project team representatives to develop and oversee clinical project strategies, plans and timelines in partnership with line function leaders • Leading strategic working groups centered on integrating and analyzing large-scale patient “omics” data sets to identify new indications, endpoints, and responsive patient sub-populations • Providing thought leadership with other BMD TAHs to identify synergies and drive innovation across our large and diverse clinical portfolio • Implementing strategies in close collaboration with the BMD global organization which includes over 100 associates with expertise in all aspects of biomarker science i.e. genetics, genomics, molecular and cellular, digital devices, imaging and data sciences This position can be in Basel, Switzerland or Cambridge MA, USA. Please state in your application letter which location you would like to be considered for. Minimum requirements What you’ll bring to the role: • MD degree required, plus additional PhD / postdoc or equivalent level research • Scientific excellence supported by recognised high quality publications; clinical expertise in hepatology, renal, hematology or rare diseases (Board Certified or similar level preferred) • Experience performing similar role within a pharmaceutical/biotechnology research company, clinical research organization or academic medical center • Significant relevant experience after your MD / PhD / postdoc including quantitative expertise in biostatistics, bioinformatics, computer biology, statistical genetics, machine learning, or data science; hands-on analyzing, interpreting and publishing studies consisting of “omics” data e.g. genetics, genomics, proteomics; closely partnering with/leading data scientists • Proven success in leading matrix (global, cross functional) teams including well-developed interpersonal, communication (oral and written) and influencing skills • Creative and innovative leadership with a sharp and objective intellect • Human genetics or clinical imaging experience is desirable • Business-level / fluent English (oral and written) Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network: https://talentnetwork.novartis.com/networkDivisionNIBRBusiness UnitTranslational MedicineLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

29.07.2020

Novartis AG

Lab technician for in vivo PK studies

  • Novartis AG

  • 4040Basel

  • 29.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID299029BRPosition TitleLab technician for in vivo PK studiesApply to Job Job Description 6000! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Your responsibilities include, but are not limited to: • Conducting high-quality routine PK studies in rodents independently, this involves also to record and document experimental details with a high level of integrity, ethics and accuracy. • Executing basic surgery in rodents including anesthesia and analgesia • Complies strictly with Swiss and Novartis-specific Animal Welfare Regulations as well as adopts and applies 3R rules to daily business. • Pro-active and innovative team member • Able to maintain an in vivo experimental laboratory Minimum requirements What you’ll bring to the role: • Completed education as Laboratory Technician in Biology, Biochemistry or related discipline (or alternative professional work experience in a relevant scientific field) • Basic education in animal handling necessary (LTK1 course, Felasa Cat. B or equivalent) • Good skills in animal handling, anatomy, anesthesia, basic surgical knowledge in rodents, a high level of proficiency in various rodent dosing techniques, the preparation of formulations for administration and biological matrices for further analysis. • Fluency in English and German • Good knowledge of MS Office Tools Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitTranslational MedicineLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeTemporaryShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.07.2020

Novartis AG

Global Head HSE Strategy & Innovation

  • Novartis AG

  • 4051Basel

  • 28.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID297843BRPosition TitleGlobal Head HSE Strategy & InnovationApply to Job Job Description 108,000! That’s the number of associates whose lives HSE touches and improves. Join us in our mission to protect our people, patients and planet as part of the Novartis Health, Safety and Environment team. Reporting to the Global Head HSE, you are responsible for HSE strategy and innovation transformation / change across Novartis globally – approximately 109,000 employees across the world in mixed workplace environments including scientific disease research labs, offices and sophisticated manufacturing / production sites. HSE has 300 professionals, and Novartis has permanent HSE presence in 70 countries. Yours is an important leadership position: forward-looking HSE innovation across a large global company, introducing the most advanced HSE strategies that will directly improve the company’s success. --- This position can be in Dublin, Prague, a major US city or Basel: please let us know in your application letter the locations you would like to be considered for. Novartis provides international family relocation --- Your key responsibilities • Partner closely with the Global Head HSE to define the global Novartis HSE strategy & approach to innovation with your inspiring leadership. You are an HSE Thought Leader and fully accountable for global HSE strategy and innovation. You will translate the HSE strategy into functional objectives and activities, evaluate progress against the overall strategy, and identify and initiate special projects whilst ensuring stakeholder involvement throughout. You will drive innovation by how you craft the HSE strategy then refine it through new initiatives and anticipation of internal and external change drivers • Member of the Global HSE Leadership Team (6 members) and the REFS Strategy & Alliances Leadership Team: partnering with peers to achieve the best global HSE strategy, with subject matter experts from across different regional teams (including CBRE and other 3rd party providers) to ensure innovative programs have global success. Facilitates the Global HSE Council to fully integrate HSE strategy into the overall business function plans • Set the global agenda across all types of business partners; key HSE objectives; resource & budget planning, footprint and integration/ engagement planning management with all business groups • Deliver global HSE technology innovation strategies including partnerships with universities and start-ups, advising REFS and global business functions on strategies to maximize HSE innovation in Novartis • Develop a communications and engagement strategy & material with close consideration of the needs of multiple and diverse internal and partners. Develop and lead a global HSE partner network to engage with, establishing closer relationships with NGOs, government entities and other institutions on HSE matters important to Novartis that impact them. These may include advances in understanding and use of big data, machine learning and predictive analytics in HSE; total worker health; also local topics within countries • Lead all aspects of governance to ensure systems are in place that demonstrate and verify compliance with HSE regulations, permits, statutes, local ordinances and other externally driven requirements • Role model a leadership style that is inclusive, proactive, respectful, change agile, innovation/creativity, and achieve results with a strong customer service focus • Strengthen the operational aspect of HSE; delivering an approach to reducing functions process/organizational complexity that provides better transparency • Implementation responsibilities: HSE strategy, innovation, governance, communications and engagement, operational execution of strategic programs, alliances and key partnerships to deliver global HSE services contract; COVID-19 has accelerated the significance of the wide range of strategic Novartis HSE change programs already underway globally, including moving from defined technical procedures and regulations towards a people-focused approach enabling employees to take care of their HSE. The health & safety of our employees is of primary importance and your expertise and leadership will us ensure this. Minimum requirements What you'll bring to the role: • • University degree in safety engineering, safety management, industrial hygiene, environmental science, occupational health and/or medicine, engineering, or related field: Master’s degree or higher is strongly preferred • Significant HSE expertise from working within multi-national organizations at senior levels. You are known within the professional HSE community for your strategic thinking and innovative approaches that have evolved approaches to HSE. You’ve led strategy and planning for multiple high impact regional / global HSE change programs that included operational efficiency and process improvements, and that achieved demonstrable success modernizing your organization’s HSE and directly benefitting business outcomes • In-depth knowledge of international management system standards for HSE (e.g. OHSAS 18001, ISO 14001, ISO 22301, ISO 31000, ISO 50001). • Very strong people, business leadership and senior stakeholder management experience, used to leading and working with diverse regional teams and remote business relationships. You communicate effectively across organizations with a high level of personal credibility, customer relationship management, and networking: successfully identifying and managing diverse stakeholders thanks to your superior interpersonal / influencing skills. You are skilled at quickly understanding and being successful within an organization’s culture Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network: https://talentnetwork.novartis.com/networkDivisionNBSBusiness UnitREFS NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaFacilities & AdministrationJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.07.2020

Novartis AG

Senior Expert Epidemiologist (80-100% )

  • Novartis AG

  • 4040Basel

  • 28.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID296093BRPosition TitleSenior Expert Epidemiologist (80-100%*)Apply to Job Job Description 80! The Quantitative Safety & Epidemiology team is responsible for 80 Novartis products! We are an interdisciplinary group in the global Patient Safety organization, and we help regulators, physicians and patients to understand the benefits and risks of assigned drugs, by asking the right questions and by applying the most appropriate scientific methods. As Senior Expert Epidemiologist you will shape the epidemiology strategy of one or several drugs within a designated therapeutic area, and across the development life cycle. Responsibilities will include but are not limited to: • Owning the implementation of innovative epidemiology approaches to evaluate the safety and benefit-risk profile of a drug based on data from multiple sources • Designing, executing and reporting epidemiological studies using real-world databases and providing the scientific oversight for other non-interventional studies. • Evaluating published evidence and positioning epidemiology information in context using quantitative methods and data visualizations. • Providing scientific and methodological expertise on relevant data sources, study designs and analysis methods to evaluate safety risks and risk management activities. • Responsibility for epidemiological sections of documents for Health Authorities • Proposing and implementing improvement initiatives internally and externally in collaboration with epidemiology professionals in academia, industry and regulatory agencies Minimum requirements What you'll bring to the role: • Master’s degree or equivalent in epidemiology or related areas (PhD preferred) • Fluent English (oral and written) • 10+ years of experience in positions of growing responsibility in the Pharmaceutical Industry with 6+ years applying epidemiological principles and methodologies to drug development and life cycle management. • Proven experience in leading scientific improvement/ change initiatives / direct reports. Excellent strategic skills. Natural leadership style with the ability to build successful partnerships at all levels • Scientific curiosity combined with strong communication skills bridging scientific and business needs over different expertise areas • Experience in designing, conducting, analyzing and interpreting epidemiological studies and working with large electronic health records databases. Computing ability, including knowledge of specialized epidemiological/statistical packages (advanced level, SAS or R experience desirable). *Some restrictions on flexible working may apply and will be discussed at interview if applicable Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitCMO & PATIENT SAFETY GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.07.2020

Novartis AG

Head Advanced Analytics Solutions, Data & Digital Oncology

  • Novartis AG

  • 4051Basel

  • 28.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID297273BRPosition TitleHead Advanced Analytics Solutions, Data & Digital OncologyApply to Job Job Description 1 of Novartis 4 strategic priorities. Join the new Global Oncology Data & Digital team that will drive the digital transformation across countries and help with our bold vision to cure cancer! The Head Advanced Analytics Solutions demonstrates his/her strong business leadership experience across functions to identify use-cases and convince functional and operational leadership to develop and implement advanced analytics solutions ultimately redefining the way we operate. He/she is responsible for effectively expanding new and existing sophisticated analytics use-cases that drive insights and empowers effective, data driven decision-making for the Oncology Business Unit (OBU). This position plays a critical role in analytics governance, in the alignment with data and digital teams and effective coordination of high impact deliverables in line with OBU strategy and priorities. Your responsibilities: Your responsibilities include, but are not limited to: • Develop, prioritize, accelerate and support Advanced Analytics (AA) use-cases in close collaboration with Global, Regional and key-Country business partners and the Novartis Group Center of Excellence (CoE) for Data Science and Artificial Intelligence (DSAI) • Work collaboratively with Global functional leadership (e.g. Medical and Commercial Franchise Heads, Real-World Evidence (RWE), Business Excellence, Insights, OBU Data Science CoE as well as with key markets to identify and prioritize use-cases for the development and application of AA/Data Science • Drive portfolio use-cases in close collaboration of Group DSAI CoE, functional and country teams with scaling of prioritized initiatives in mind • Lead AA enablement strategy and build capabilities for AA and Data Science among business users across the organization in close collaboration with DSAI CoE, OBU Data Science CoE and OBU capabilities teams • Demonstrate broad functional understanding of operating models, including but not restricted to Brand Management, Sales Management, Business Excellence, Medical Affairs, Insights, RWE, BD&L, Competitive Intelligence and Finance to work optimally in a matrix organization • Perform effective leadership and transformational management, demonstrating high skills in organizational change, persevering to overcome issues, balance risks, building robust teams and building trust among partners • Utilize and build positive relationships to coordinate with other analytics functions and Data Science teams across Novartis • Work together with the Global Data & Digital team to ensure that the OBU utilizes the acquired data efficiently and optimally to drive governance and prioritization of projects and AA enablement in order to continuously meet business goals and answer business questions from senior leadership Minimum requirements What you’ll bring to the role: • Strong experience as operational and cross-functional business leader in pharma industry, ideally as General Manager, Franchise Head and/or in Business Excellence • Strong demonstration of experience and/or education in analytics and data science and/or decision sciences supporting and prioritizing business s questions and recommendations • Proven track record to manage multiple projects, to be accountable for individual & team results and drive change across multiple countries and functions • Broad functional understanding of operating model will be essential, including but not restricted to Brand Management, Sales Management, Business Excellence, Medical Affairs, Insights, RWE, BD&L, Competitive Intelligence and Finance • Minimum 10 years of healthcare experience required, incl. leadership experience managing, mentoring and growing teams • Ability to establish relationships, collaborate and influence across a multi-country and multifunctional matrix organization; • Demonstrated prioritization, organizational, analytical and research skills as well as the ability to conceptualize more sophisticated issues and work on complex processes, procedures or solutions Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Novartis are an equal opportunities employer and welcome applications from all suitably qualified persons Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

27.07.2020

Novartis AG

Drug Product Project Leader Parenteral Dosage Forms (80-100% )

  • Novartis AG

  • 4040Basel

  • 27.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID296994BRPosition TitleDrug Product Project Leader Parenteral Dosage Forms (80-100%*)Apply to Job Job Description ~350! This is the number of associates in Global Pharmaceutical Development around the globe, working tirelessly on innovative and patient centric pharmaceutical dosage forms for oral, parenteral, topical and inhaled administration routes. For the Development of our small molecule parenteral projects, we are looking for a Drug Product Project Leader. As a member of Pharmaceutical Development (PHAD), you will represent PHAD in global project teams and define the global Formulation and Process Development strategy of the assigned project(s). With your energy, you will shape the future of the Novartis small molecule portfolio and bring our molecules to our patients! Your responsibilities will include but are not limited to: • Lead and manage Formulation & Process development activities, including process optimization, scale up and validation applying QbD principles in line with the overall project strategy of the global project team with a focus on RNA and oligonucleotides related projects. Experience in late phase development for sterile products, e.g. Ophthalmics, is advantageous. • Seek alignment with departments and functions in and outside of own department (e.g. Analytical Research and Development, Clinical Supply, QA), and proactively communicate the overall project strategy, key issues and other critical topics in a timely manner to the appropriate management level, customer and stakeholders. • Drive the resolution of technical challenges in a timely fashion. • Lead the Drug Product team(s) in a complex international matrix organization and in line with the culture, values and behaviors of Novartis • Be accountable to meet quality, timelines and budget for assigned projects. • Manage interactions with internal and external stakeholders. Minimum requirements What you will bring to the role: • Education: Ph.D. in pharmaceutical technology or related science. Language: Excellent English required (oral & written). Local language advantageous. • Minimum of 7+ years of experience within the pharmaceutical industry, preferably in late phase development for sterile products and oligonucleotides. • Excellent knowledge of the Pharmaceutical Development (formulation and process development) is required. • Proven 5+ years of leadership experience in managing complex development projects, ideally in a global matrix environment. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

27.07.2020

Novartis AG

Senior Principal/ Principal Statistical Consultant (80-100%)

  • Novartis AG

  • 4040Basel

  • 27.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID298853BRPosition TitleSenior Principal/ Principal Statistical Consultant (80-100%)*Apply to Job Job Description 20+ world-class experts in the fields of statistical methodology and modelling & data science! We work as internal consultants to support our entire drug development portfolio and collaborate at the scientific interface with other external partners across industry, academia and regulatory agencies. As a Senior Principal/ Principal Statistical Consultant you will work in collaboration with Biostatisticians, Pharmacometricians, Global Project Teams and senior Advanced Methodology & Data Science (AMDS) colleagues to ensure the use of state-of-the-art statistical methods, models and machine learning are used at the trial and project level. You will contribute towards the professional development of Biostatistics and Pharmacometrics group members. Your responsibilities will include: Project level: • Provide trial and sometimes project support requiring hands-on expertise in novel quantitative approaches. This could include: innovative clinical trial design, quantitative decision making, incorporating evidence from sources of big data (e.g. biomarkers, digital technology and real world evidence) • Support the implementation and communication of innovative quantitative methods to support regulatory submissions and health authority meetings Scientific Innovation and Training: • Help developing new quantitative methods with the aim of improving drug development at Novartis in multiple projects. The focus includes clinical trial design, modeling, visualization and machine learning • Support evaluating the need of technology and novel scientific software, visualization tools and new approaches to computation to increase efficiency and quality of Novartis drug development practices External Engagement: • Publish in peer reviewed journals, participate in professional conferences and contribute towards cross-industry work streams in external scientific working groups Minimum requirements What you’ll bring to the role: • Ph.D. in statistics, biostatistics, data science, computational biology or another related field • Fluent English oral and written • At the Principal level you will have at least 1 year of experience with application of innovative quantitative methods in drug development setting and at the Senior Principal level at least 3 years of experience. • Knowledge in relevant quantitative approaches • Ideally some experience in facilitating and optimizing the (early/full) clinical development strategy by using expertise in design, modeling or analytics • Proven interpersonal and communication skills (verbal and written) bridging scientific and business needs. • At the Senior Principal level, scientific publications and training courses given in the area of quantitative science • Good business ethics, communication and presentation skills Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitCD&A GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

27.07.2020

Novartis AG

Senior Strategy & Technology Leader-Downstream

  • Novartis AG

  • 4051Basel

  • 27.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID294243BRPosition TitleSenior Strategy & Technology Leader-DownstreamApply to Job Job Description 1st! Novartis is industry leading in the area of continuous manufacturing and integrated bio-manufacturing. We are well recognized for leading the development and implementation of continuous manufacturing for small molecules and are also leading in the implementation of the first commercial integrated and continuous processes for large-molecule biologic. Your role will drive the leading edge development of Integrated and Continuous manufacturing for Novartis Biologics. You will be joining a dynamic team of forward-thinking scientific leaders, leading the development and implementation of the next-generation of biopharmaceutical process technology. In this role, you will lead and manage an Innovative Process Technology team with the purpose of defining and implementing the “next generation” bioprocess development program and manufacturing technologies, within Novartis Biologics. Apply scientific/technical expertise to drive cross-functional and cross-departmental alignment and further evolve the Drug Substance development, manufacturing, and control strategy of Biologics at Novartis Pharma AG. You will develop long term scientific and technology strategies to support high productivity, high throughput biologics processing and manufacturing. Your responsibilities will include: • Responsible to lead a sub-team charged with developing disruptive technologies and designing a strategic paradigm shift in the development of biologic drug substance processing, to enable fastest delivery to the market. • Set strategic priorities for the functional sub-team, aligned to deliver the overall global strategic initiative goals. • Lead a program to set the direction and foundation for all future drug substance development activities within TRD. • As a core team member of a global strategic initiative, develop strategies, novel technologies and drug substance manufacturing processes for the clinical and commercial production. • Work closely with the NTO manufacturing sites to drive value through the implementation of impactful technology across modalities and formats. • Ensure the alignment of cross-departmental functions to ensure global implementation, including integration with drug product processes. • Indirect management and mentoring of several associates and function leaders. • Understand resource constraints and identify/lead cost saving opportunities. • Support technology evaluations and proactively identify/realize opportunities for Intellectual Property in the product portfolio and technology projects. Minimum requirements What you’ll bring to the role: • PhD or equivalent education in Biology, Biochemistry, Chemistry, Chemical Engineering or a related discipline • Fluent English required (oral & written); good skills in German as local site language (oral), desired • At least 10 years of experience in the development of downstream processes for biopharmaceuticals (DS process development & manufacturing process); experience in late phase development and commercialization is highly desirable. • Hands-on experience in high productivity harvest, capture, and purification process design for biopharmaceuticals is required. Previous experience with integration of new technologies into a manufacturing environment is advantageous. • Experience in filings with health authorities, preferably with BLAs/MAAs • Understanding of quality control (cGMP) including production aspects • Experience in design of experiment (DoE) and use of statistical programs • Demonstrated ability to work in interdisciplinary technical teams • Excellent communication skills and organizational skills • Propensity for scientific and entrepreneurial think Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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26.07.2020

Novartis AG

Global Trial Program Head

  • Novartis AG

  • 4051Basel

  • 26.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID299522BRPosition TitleGlobal Trial Program HeadApply to Job Job Description With over 400 active trials in 5 hub countries, Novartis GDO Trial Management feels privileged to bring together and manage all aspects of clinical trial operations reaching around 50 000 patients worldwide. We are a proactive learning organization and we place a lot of emphasis on collaboration and individual development. As part of this we are very committed to evaluating the latest digital technologies, always looking to transform trials and improve lives. TM is in search of those who are passionate about applying their experience to reimagine clinical trial operations and ultimately improve the lives of our team, our organization and our patients. We are Novartis. Join us and help us reimagine medicine. The Global Trial Program Head leads planning and management of the assigned clinical program(s) from an end-to-end trial management perspective to achieve Global Program Team (GPT), Global Clinical Team (GCT) and GDO-TM objectives. Complete oversight of budget and resource allocation within assigned clinical program(s) – including broader review of resources across programs. Acts as GDO representative on GPT. Drives operational excellence through process improvement and knowledge sharing across clinical programs within franchise. Enables an empowered organization, which can navigate in a matrix environment and adjust quickly to business needs. Point of escalation for resolution of trial management operational issues within assigned program(s). Your responsibilities include, but are not limited to: 1. Build best talent and an inspired, curious and unbossed culture to foster high performance in a matrix environment. • Responsible for overall management of trial management associates working on assigned program(s) including hiring, trainings, coaching, performance management and career development; • Drive functional excellence in education, implementation and compliance to best practices and share lessons learned for trial management. 2) Resource and Budget Management: • Ensures optimal resourcing across trials within assigned program(s) to meet business needs according to portfolio prioritization. Collaborates with Franchise Head TM including coordination of headcount requests and resource alignment with other line functions; • Oversee life cycle budget including forecast, year cost targets, and annual cost targets for all trials within assign program(s). Full accountability for clinical work package pre-GTD assignment. 3) Program level planning and execution: • Key contributor to operational strategy within assigned program(s); provide global clinical operational input into Integrated Development Plans (IDP) for assigned program(s); • Drives timely and efficient program execution according to the approved IDP; • Establishes program and trial priorities in alignment with Franchise/GPT/GCT priorities ; • Develop and implement operational program-specific standards as required to enhance consistency across trials. 4) Core member of the Global Clinical Team (GCT). GDO representative on GPT (extended member). Acts as liaison between GPT and Trial Management/GDO – including point of escalation for resolution of trial management operational issues within assigned program(s). 5) Identify and build center of excellence in clinical trial execution by developing process standards and tools to achieve excellence in trial management. Drive process improvement in collaboration with the Global Head Center of Excellence for Trial Management, other Global Trial Program Heads and Trial Management Franchise Head. 6) Provide oversight on quality and compliance for assigned clinical program(s) in conjunction with the Head of Process Control Managers. Minimum requirements What you’ll bring to the role: • Bachelor’s Degree required and Advanced Degree is preferred • A minimum of 10 years of pharmaceutical clinical research experience is required • A minimum of 5 years people management and development experience is required; this may include management in a matrix environment • Demonstrated leadership and accomplishment in all aspects of conducting global clinical trials and programs • Extensive knowledge of clinical development process, GCP and clinical project management • Organizational awareness, including significant experience working cross-functionally and in global teams Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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26.07.2020

Novartis AG

Global Head, Digital Health Solutions Oncology

  • Novartis AG

  • 4051Basel

  • 26.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID297274BRPosition TitleGlobal Head, Digital Health Solutions: OncologyApply to Job Job Description 1 of Novartis 4 strategic priorities. Join the new Global Oncology Data & Digital team that will drive the digital transformation across countries and help with our bold vision to cure cancer! The Global Head, Digital Health Solutions: Oncology will be an exciting opportunity to develop and implement our around-medicine, beyond-medicine and digital therapeutics portfolio the Novartis Oncology team, which aligned with our Digital Vision and Strategy. Our Global Head of Digital Health Solutions will be responsible for the development of a team that identifies digital opportunities along our patient journey to enhance strategy and drive implementation of important digital & data initiatives. At the heart of this opportunity lies the development and implementation of digital solutions in multi-functional collaboration. Through your understanding of decision journeys you can address patient needs, improve patient outcomes and have a positive impact. You’ll play a meaningful role in providing innovative solutions across diseases areas and geographies with groups that include patients, physicians and nurses. If you’re a creative problem solver with a passion for all things digital, then why not consider an application to our Global Head of Digital Health Solutions: Oncology role today?! Your responsibilities include, but are not limited to • Identifying, generating, prioritizing, accelerating and aligning DHS platforms that can be scaled across multiple countries and disease areas in the fields of groundbreaking patient support programs, apps and wearables, in coordination with tech industry leaders • Conducting innovation workshops with Global and key-Country disease teams to identify round-medicine, beyond-medicine needs & opportunities, screen and prioritize them • Building cross-country coalitions to drive the end-to-end implementation and scaling of a portfolio of 10-15 DHS, across markets, brands and functions in a complex matrix organization • Driving our team to be a preferred Oncology DHS partner thanks to agile execution and strong partner networking among HealthCare Practitioners, HealthCare Services, patients and digital companies. • Guiding the team’s direction, maintaining overview of planning, progress, quality and budget • Using the power of data, digital/social innovation to inspire and develop cutting edge solutions to our customers that can include elements across multiple platforms, touchpoints, devices, apps, databases and channels • Ensuring interactivity with patient and physician databases and other interfaces as an integral part of our digitalized customer journeys with deeper insights Minimum requirements What you’ll bring to the role • University Degree in related field, MBA or Master's Degree preferred • 10+ years of experience in defining and implementing DHS that address customer needs and build a distinctive customer experience, with a track record in pharma and healthcare sector • Excellent leadership, collaboration and people management skills. • Proven project leadership skills in sophisticated multi-functional and multi-country environment • Ability to build extensive internal and/or external networks to enable digital innovation • Deep practical understanding of digital innovation methodologies • Solid experience in driving multi-functional, cross-country digital projects, with clear measurements, service mentality and solution-orientation • Strong analytical skills • Good interpersonal skills, communication and presentation skills • Good understanding of business and, IT and digital implementation • Curiosity, at ease with uncertainty and ambiguity, ability to work independently and deliver in a global matrix environment, collaborating with a variety of external and internal partners • Strategic mind-set: Ability to speak multiple business languages (strategy, innovation, marketing, technology); excellent planning and strategy development while executing against tight Desirable requirements • Experience in Agile methodologies Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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26.07.2020

Novartis AG

Head of Strategy & Operations, Data & Digital Oncology

  • Novartis AG

  • 4051Basel

  • 26.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID297272BRPosition TitleHead of Strategy & Operations, Data & Digital: OncologyApply to Job Job Description 1 of Novartis 4 strategic priorities. Join the new Global Oncology Data & Digital team that will drive the digital transformation across countries and help with our bold vision to cure cancer! Our Head of Strategy & Operations, Data and Digital Discovery presents an exciting opportunity to have a meaningful positive impact within our Oncology team. In this role, you’ll support the team’s strategic objectives through innovation and exploration of imperatives within the overall Novartis Oncology, Global Digital & Data vision. You’ll navigate through global and regional markets on challenging data and digital topics related to areas that include Data Science, Artificial Intelligence, Omni-channel Engagement and Digital Health Solutions. The Head of Strategy and Operations, Data & Digital will help us to create the future we want, nurturing multiple digital capabilities end to end, from definition to workshops and delivery. As a strategic leader, the long-term roadmap for the Oncology team is in your hands and through collaboration with Senior Leadership, you will help to spread digital excitement across our Novartis community. If you are excited at the prospect of implementing cross-country and cross-functional strategies in digital & data then why not consider an application to our Global Head of Strategy and Operations, Data & Digital: Oncology role today! Your responsibilities include, but are not limited to • Developing a Global Digital & Data strategy in close collaboration with our Oncology strategy department, Novartis Chief Digital Office and Oncology Digital & Data Leadership Team across functions and countries • Drive cross-functional and cross-country projects to implement the strategy in the areas of our operating model, Agile ways of working and other fields related to: Omnichannel Customer Engagement, Digital Health Solutions, Data Science and Artificial Intelligence with commercial and medical teams • Work in close collaboration with the Global Digital and Data leadership Team, People & Organization team and capability building teams to develop and roll-out Digital & Data capabilities across the organization and the implementation of a solid Digital & Data talent mapping and talent development program • Work closely with Digital & Data Leadership Team and internal communications to drive digital engagement and excitement across the organization • Collaborate within Global Head, Oncology Data & Digital and Finance to develop and monitor Global Digital & Data budget allocation • Development and systematic implementation of agile methodologies in relevant functions across the team Minimum requirements What you’ll bring to the role • University Degree with an advanced degree in Science and/or Business preferred (MBA/PhD) • Strong analytical ability, strategy/consulting background with experience in data & digital initiatives strongly preferred • Strong project management skills; experience at driving global cross-functional projects at Business Unit Level preferred • At least 5 years of experience in healthcare discipline, strategy consulting or Oncology company with global understanding of pharma business and healthcare industry, across various disciplines/functions (e.g., commercial/medical, payors, providers and development) • Tech savviness and aptitude to lead and drive innovative marketing and operation initiatives and expansions with a critical focus on performance as well as identification, evaluation and incorporation (where applicable) of emerging technologies and trends into Oncology Business Unit • Ability to communicate effectively with senior management and ability to influence without authority • English: Proficient in oral and written Desirable requirements • Knowledge of Agile methodologies Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

25.07.2020

Novartis AG

R&D Chemist, Oligonucleotides (80-100% )

  • Novartis AG

  • 4051Basel

  • 25.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID294172BRPosition TitleR&D Chemist, Oligonucleotides (80-100%*)Apply to Job Job Description More than 50! synthetic steps look for the future design of a manufacturing process delivering quality oligonucleotide drugs at large scale. As a highly skilled and creative chemist you will take a leading role to ensure long-term supplies to our patients. The position is within the Global Technical R&D department of Global Drug Development. Within this organization Chemical & Analytical Development (CHAD) plays an essential role in the development of processes for manufacturing and analysis of small molecule, semi-synthetic large molecule, peptide and oligonucleotide drug substances. Your responsibilities: • With your strong expertise and creativity in development of manufacturing processes you take a leading role in defining future manufacturing processes and strategies for oligonucleotide projects • In our labs, your experimental designs will be executed and allow you to interpret and report data and results • As a core member of cross functional team, you collaborate closely with our internal and external partners to ensure timely and quality delivery of new oligonucleotide drugs to our patients • Provide relevant process documentation in support of filing of dossiers • Actively participate in scientific exchange groups within Novartis and Academia as well as maintain excellent collaborations with our customers Minimum requirements What you’ll bring to the role: • Scientific curiosity coupled with recognized achievements in the field of oligonucleotide chemistry • Dedicated, thoughtful and flexible team working skills • Good knowledge of English (oral and written) is required, good command of German (spoken/ written) is desirable • Excellent knowledge of laboratory and/or technical tools • Good knowledge of office software and computer tools such as Office package Desirable Requirements: • We are looking for candidates with PhD and PostDoc in Synthetic Chemistry or equivalent with specialization in the field of oligonucleotide synthesis • A minimum of 5+ years relevant professional experience in chemical process development for oligonucleotides is required. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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25.07.2020

Novartis AG

Senior Manager Digital & IT Audit

  • Novartis AG

  • 4040Basel

  • 25.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID280971BRPosition TitleSenior Manager Digital & IT AuditApply to Job Job Description Internal audit aspires to be a trusted assurance and advisory provider, and a talent pool driven by purpose to better support the business in serving our patients. The Digital & IT Audit Role within Internal Audit offers you an opportunity to develop leadership skills, business acumen, and risk awareness through hands-on audit engagements within NBS, NBS IT, CDO and the wider Novartis business. You will benefit from exposure to new areas around business and technology transformation, risk-based decision-making and evaluation of company controls. Furthermore, you will have opportunities to engage with senior leaders across the Novartis organization and develop skills around conducting risk assessments and leading advisory engagements to help the organization meet its objectives. In addition, Internal Audit actively supports your development with training and coaching to enhance your auditing and leadership skills. You will be responsible but not limited to: • Lead effective audit and advisory teams throughout assignments in different divisions and functional areas taking responsibility for the team members • Support members of the team with your knowledge of Digital and IT, including those in other functional and regional groups. • Understand key company policies that IA provides assurance on, including their implementing guidelines and procedures. • Auditing Enterprise Architecture (EA) from conceptualization, design, implementation to adherence. Provide reasonable assurance on conformance and compliance of Technology/Business projects and programs with architect guidelines and standards. Hence confirming that the “Voice of the customer” is at the core of these transformation projects/programs. • Reviewing and evaluating internal technical (IT, Digital, Technical Operation) functions development strategies, processes, programs and recommending improvements • Identify root causes of control issues. Investigate, analyze and test possible solutions or measures for improvement. • Prepare audit and advisory reports, review and agree issues with responsible management. • Establish and maintain key-contact relationships with the management in functional areas of responsibility to support NBAA and Internal Audit in assessing risk and developing the annual audit plan. • Lead the risk-prioritized planning of standard operational audits and support the Head of Digital, NBS and GCF Audit in the planning of complex audits on enterprise risks without pre-defined control frameworks. • Build effective business partnering and advisory relationships with senior management and with managers in the relevant functions, while maintaining the independence and objectivity of self, team and the IA function. Perform special projects and lead advisory initiatives to support the organization. • Coach team members and guest auditors, and provide technical support and feedback. Minimum requirements • Degree in Business Computing, Information Technology, technical or scientific area. Further qualifications in systems architect, development, data science, service delivery, project management. • Fluent in English, other languages desirable. • Experience as Enterprise Architect (technology and business architect) with modern technologies • Work experience in digital projects and transformations, business and IT transformation, IT operations, system development life cycle, IT risk management, information governance and business relationship management. • Experience and ability to act in a complex and rapidly changing business environment, including leadership experience in managing teams and projects. • Strong communication and interpersonal skills. • Willingness to travel (~40%+). WHY CONSIDER NOVARTIS? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis!DivisionCORPORATEBusiness UnitBUSINESS ASSURANCE AND ADVISORYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaAudit & FinanceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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25.07.2020

Novartis AG

Analytical Expert Oligonucleotides (80-100% )

  • Novartis AG

  • 4040Basel

  • 25.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID294171BRPosition TitleAnalytical Expert Oligonucleotides (80-100%*)Apply to Job Job Description More than 50! Sophisticated analytical methods and platforms devices are required ensure successful manufacture high quality drugs at large scale. You will take a leading role defining future standards for analytical control of oligonucleotide drugs ensuring long-term supplies of our patients. The position is within the Global Technical R&D department of Global Drug Development. Within this organization Chemical & Analytical Development (CHAD) plays an essential role in the development of processes for manufacturing and analysis of small molecule, semi-synthetic large molecule, peptide and oligonucleotide drug substances. Your responsibilities: • With your strong expertise and creativity in analytical development, you take a leading role in setting up future analytical control strategies and standards for oligonucleotide projects • In our labs, your experimental designs will be executed and allow you to interpret and report data and results • Coordinate and plan all cGMP related activities for starting materials and intermediates to ensure timely manufacture under GMP within Chemical & Analytical Development • Being a core member of cross-functional team. Collaborate closely with our internal and external partners to ensure timely and quality delivery of new oligonucleotide drugs to our patients • Provide relevant process documentation in support of filing of dossiers • Actively participate in scientific exchange groups within Novartis and Academia as well as maintain excellent collaborations with our customers Minimum requirements What you’ll bring to the role: •Scientific curiosity coupled with recognized achievements in the development of new analytical methods using advanced separation and detection technologies (e.g. UHPLC, SEC, IX, IP, SFC, 2D-LC, CAD, and related hyphenated techniques including high resolution MS • Dedicated, thoughtful and flexible team working skills. •Good knowledge of English (oral and written) is required, good command of German (spoken/ written) is desirable. •Excellent knowledge of laboratory and/or technical tools •Good knowledge of software and computer tools such as Office package Desirable Requirements: • We are looking for candidates with PhD and PostDoc in analytical chemistry with specialization in the field of oligonucleotide analytics. • A minimum of 5 years relevant professional experience in field of analytical development for oligonucleotides is required. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

24.07.2020

Novartis AG

Qualification Expert (80-100%)

  • Novartis AG

  • 4040Basel

  • 24.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID298826BRPosition TitleQualification Expert (80-100%)*Apply to Job Job Description 600! This is the number of instruments you and your colleagues from the Qualification team will take care of to ensure highest quality and compliance to cGMP guidelines of all our analytical equipment used to enable the testing of our biological medicines. In this role, you will be part of the Qualification and Logistics team and together with your team, you will support the qualification of all analytical equipment in Biologics Analytics Operations (e.g. HPLC, CE, KF, pH-Meter). You will work closely with your team members as well as with Scientists of various teams and Quality Assurance. We are a collaborative team, helping each other is a matter of course. Your responsibilities include but are not limited to: • Initiate, support and supervise qualifications of analytical equipment, including Computer System Validation (CSV), in close collaboration with the analytical laboratories • Act as System Owner for analytical laboratory instruments. • Write and review documents related to your field of work (e.g. SOPs) to ensure compliance to global guidelines. • Contribute to evaluation of new scientific technologies/equipment • Ensure compliance to cGMP and HSE according to applicable regulatory requirements and guidelines. Support Health Authority inspections and Audits. • Actively participate in global teams, projects, networks and/or platforms Minimum requirements What you’ll bring to the role: • Apprenticeship, BSc or MSc in Chemistry, Biology or similar field • Several years of work experience in qualifying laboratory instruments and Computer System Validation in a GMP environment is a must • Good knowledge on relevant regulatory guidelines and good understanding of regulatory expectations • Fluent in English (oral and written). German is desirable • You are a team player with very good communication skills Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

23.07.2020

Novartis AG

Executive Director-DSAI Strategic Alliance

  • Novartis AG

  • 4051Basel

  • 23.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID295277BRPosition TitleExecutive Director-DSAI Strategic AllianceApply to Job Job Description 2020 is an exciting year for Novartis as we accelerate our growth in the digital space. The Executive Director-DSAI Strategic Alliances is a senior leader responsible for forming and leading the Strategic alliances for Novartis. This includes leading the effort towards evaluating the needs of Novartis BU across the enterprise, identifying potential strategic partners, leading the contracting process, establishing effective governance post contracting and ensuring strong relationship with key stakeholders across Novartis and partners. Your responsibilities: Your responsibilities include, but are not limited to: • Lead the effort to identify and evaluate potential strategic partners in the Industry • Align stakeholders across Novartis on the potential of such a partnership and lead the contracting process across functions • Establish effective partnership governance post contracting • Build strong relationship with key stakeholders across Novartis and partners and proactively address any challenges • Support the partners and NVS stakeholders to scale the scope and nature of partnership • Generate strategic recommendations for DS&AI solutions which enable informed decisions of Novartis top leaders across business units • Develops network of senior leaders across Novartis, cross-BU, and globally, to execute on the objectives of the organization • Inspire others on culture change, the role will be expected to work with the senior leadership across our businesses and operating functions to support driving the digital trans-formation within Novartis. Minimum requirements What you’ll bring to the role: • Master or PhD in natural science or engineering or Data Science MBA from a top business school preferred English • 10+ yrs of Experience across Data Science, Strategy consulting and leading global programs • Track record of strong business impact • Deep knowledge in Pharma industry • Strong ability to influence senior resources indirectly • Proven strong analytical skills • Strong financial background • Strong track record of running operations Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Novartis are an equal opportunities employer and welcome applications from all suitably qualified persons Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network #LI-NOV = NovartisDivisionCORPORATEBusiness UnitDIGITAL OFFICELocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaBD&L & Strategic PlanningJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

22.07.2020

Novartis AG

Product Line Manager, Analysis & Reporting Scientific software

  • Novartis AG

  • 4040Basel

  • 22.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID288327BRPosition TitleProduct Line Manager, Analysis & Reporting Scientific softwareApply to Job Job Description 6,000 scientists and physicians around the world use our data & systems to reimagine medicine and create therapies that save lives. ---- Novartis Institutes for BioMedical (NIBR) is the global pharmaceutical research organization of Novartis with a mission to discover innovative medicines that treat disease and human health. Our scientists need cutting-edge, state-of-the-art computing systems and NIBR Informatics (NX) is a strategic investment into informatics capabilities and positioning to deliver systems and services that are critical to the future of drug discovery. NX is a global team of ~350 technology scientists and business professionals working across 5 sites, primarily Cambridge MA (USA) and Basel (Switzerland). - Interview with NIBR CIO: https://www.novartis.com/stories/people-and-culture/qa-new-nibr-cio-dimitris-agrafiotis ---- The Information Products and Data Sciences (IPDS) group in NX is driven to maximize the impact and value to NIBR of software and data. We deliver powerful, functional, beautiful, and integrated software solutions that create a frictionless user experience. Our organization is here to build and apply excellence in product and data management to further Novartis drug discovery. As the Analysis and Reporting Scientific Product Line Manager, you will develop and continually update a vision for a group of scientific software products that support data analysis and reporting for NIBR drug discovery. Working in collaboration with other Product Line Managers, your team will contribute to an integrated product suite. You will mentor and manage a small group of product managers who share this vision with you. You will define the standard for excellence in product management in our organization and synthesize that with your knowledge of drug discovery to create or license software that enhances and helps drive NIBR science. You will prioritize product roadmaps and direct development resources to maximize value to NIBR, and will define how we measure product success and value delivery. In this role, you will identify new product opportunities, deliver consistent, stable product operations, and meet all security, stability, usability, and performance and sustainability requirements. You will evangelize your product line, give product demos, and show the impact of your product line on NIBR science. Responsibilities include but are a not limited to • Develop a vision and roadmap for your product line, Analysis and Reporting • Manage a small team of product managers • Assess product development sprints, outcomes, and enhancement opportunities. • Achieve product line success and value metrics • Manage resources among product teams • May manage a product yourself • Establish excellence in product management practice Minimum requirements What you will bring to this role: • Minimum Bachelor’s degree in biology, chemistry, or a related scientific field: PhD preferred • 3+ years of software product management within a complex matrix environment, with experience with Agile software development • 5+ years in drug discovery or a core supporting scientific field. • Quantitative skills and the ability to use data and metrics to inform decisions • Proven ability to execute consistently, rapidly, and effectively • Outstanding communication skills • Proven experience as a mentor and team player with the ability to develop and promote a shared vision • A clear and visible set values and demonstrated integrity • Ability to travel 10% Additional - Leadership / Management As a Scientific Product Line Manager, you’ll help your direct reports succeed in their jobs, manage what they’re working on, and help them realize their career development goals. Removing obstacles and supporting your team members to prosper and grow will be an important aspect of your role. You will act as a mentor and role model in our organization, seeking, managing and retaining talent. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

21.07.2020

Novartis AG

Investor Relations Director

  • Novartis AG

  • 4051Basel

  • 21.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID290380BRPosition TitleInvestor Relations DirectorApply to Job Job Description More than $50bn of net sales, more than $12bn of net income, 155 countries where our products are sold. Join Novartis Investor Relations team and become a relationship builder, an adviser to senior management, creative with communicating strategic, operational and financial information whilst exercising judgement and pragmatism to deliver meaningful messages to all our stakeholders. This position will lead quarterly earnings process, including drafting press release and compiling interim financial report and analyst presentation; manage editing process for all materials, incorporating input from across the organization and ensuring message consistency and coherence; set quarterly calendars and write senior management commentary for earnings calls; lead implementation of investor relations communications for specific region; lead and manage support of senior management from ECN and divisions so they are aware of, and well prepared for all elements of communication with investor and analyst community; monitor external trends & macroeconomics by providing meaningful regular analysis and critical evaluations to be used by senior management; translate existing data into relevant information for senior management and Board Your responsibilities: • Draft press release and compiling interim financial report and analyst presentation. • Provide perspective on all investor communications, including annual report and other financial releases, helping craft and advance the Novartis story to address investor perceptions and needs. • Proactively, in rapid time, analyze, prepare and communicate on market moving events to inves-tor community for specific region • Strengthen relationships with our current shareholders through creation and execution of account plans, and expand our shareholder base through identification of new potential targets. • Address inquiries from investors and analysts in a timely manner, providing accurate and bal-anced information on a range of topics from financial to product-specific. Deliver aligned mes-sages that support the Novartis equity story. • Actively support Head of IR on specific projects (e.g. on presentations, analytics) • Serve and liaise with internal Divisions and work proactively to deliver high quality, accurate mes-sages for both IR team and Senior Management to use with investors and analysts. • Plan and support execution of senior management roadshows, bank conference participation, one-to-one meetings and other investor events, including capital markets days (Meet Novartis Management & R&D days) • Capture investor/analyst feedback and share with IR team and appropriate management. • Follow financial market and benchmark Novartis activities vs. peers to inform our IR strategy and messaging. Minimum requirements What you’ll bring to the role: • Ideally medical or science basic degree + MBA or finance (e.g. CFA) • Excellent English oral/written communication skills • 10 years’ experience in IR + finance + communications and ideally the healthcare industry; investment banking, research analyst or asset management with healthcare background Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitGlobal Corp. FinanceLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaAudit & FinanceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

21.07.2020

Novartis AG

Data Strategy and Governance Lead - data42

  • Novartis AG

  • 4040Basel

  • 21.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID298860BRPosition TitleData Strategy and Governance Lead - data42Apply to Job Job Description Are YOU curious? Are YOU ready to harness advanced data analytics on over 20 years of R&D data and reimagine medicine? We are looking for you! data42 is Novartis’ groundbreaking initiative that harnesses the power of R&D data in one of the largest and most diverse datasets in the pharmaceutical industry to reimagine medicines. data42 applies machine learning, artificial intelligence and sophisticated analytics to generate new insights that increase our understanding of disease and medicines, improves R&D decision-making and ultimately reimagines drug discovery and development. As the Data Strategy & Platform Governance Lead, Lead data you’ll be responsible for the strategy and governance efforts for the entire data team of data42. These strategic priorities include the ownership of data roadmaps for the program, and medium and long-term planning of the dataOS group. In the governance aspects of the role, you’ll lead the creation of many, key NVS-wide data policies, data42 group policies and their definition, refinement and implementation. Our Data Strategy & Platform Governance Lead will support the definition of the data42 platform future and this is an invaluable solution in charting the future course of the program. Flexible locations offered in Basel, Dublin or Cambridge (US). Your responsibilities include, but are not limited to • Lead all aspects of the strategic direction of the data42 dataOS team comprised of pipeline teams, data governance and semantics. • Own and run our relationship with related technology development groups across NVS • Identify key data sources of interest to data42 and maintain a roadmap of future data assets that data42 should ingest, transform and make available through its platform. This includes assets in the clinical data, omics, research, operational and real-world spaces. • Engage in medium-term and long-term planning of the dataOS team and areas of focus. • Support the evaluation of new technologies, data assets and other innovative efforts both within and outside of Novartis. These evaluations are in collaboration with data42 technical and data specialists. • Support the definition and drafting of new governance guidance and policies as needed, in conjunction with other NVS partners. Support its implementation by data42 peers and colleagues Minimum requirements What you’ll bring to the role • Advanced degree preferred (PhD, MS) in Computer Science, MIS, or Information Management or a similar field, or MBA holders with suitable data-related experience and background. • Proven experience in developing R&D data strategies, especially as they pertain to biopharmaceutical companies. • Experience implementing and managing enterprise programs around data management and governance in healthcare. • Knowledge of data governance practices, business and technology issues related to management of enterprise information assets and approaches related to data protection • Knowledge of data related government regulatory requirements and emerging trends and issues • Demonstrated consulting skills, with organizational change concepts and strategies, including communication, culture change and performance measurement system design • Knowledge of risk data architecture and technology solutions • Proficiency in English (oral and written) Why consider Novartis? 799 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

21.07.2020

Novartis AG

Semantic Technologies Lead - data42

  • Novartis AG

  • 4051Basel

  • 21.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID298886BRPosition TitleSemantic Technologies Lead - data42Apply to Job Job Description Are YOU curious? Are YOU ready to harness advanced data analytics on over 20 years of R&D data and reimagine medicine? We are looking for you! data42 is Novartis’ ground-breaking initiative that harnesses the power of R&D data in one of the largest and most diverse datasets in the pharmaceutical industry to reimagine medicines. data42 applies machine learning, artificial intelligence and sophisticated analytics to generate new insights that increase our understanding of disease and medicines, improves R&D decision-making and ultimately reimagines drug discovery and development. Our Semantic Technologies Lead will central to the success of data42, helping us to build a scalable and integrated data platform requiring multiple semantics technologies, resources and approaches. You’ll shape data42’s vision for how semantics can be practically supported to help the team achieve our mission. Collaboration within data42 is key, so we’ll appreciate your ability to coordinate the architecture and implementation of Semantics and metadata standards across all data process pipelines. Our Semantic Technologies lead will positively affect our ability to work with data, from initial ingestion right through to making data accessible via APIs. If you are excited about contributing to our digital revolution, appreciate the significance of well-indexed resources and the richness of metadata, why not consider an application today! Flexible locations offered in Basel, Dublin or Cambridge (US). Your responsibilities include, but are not limited to • Lead and coordinate pipelines teams towards implementing data42’s vision for semantics including the integration of enterprise master data management standards. • Interface seamlessly with semantic experts across the company including the CDO and others. Establish and implement the roadmap for data42 to implement the enterprise vision for semantics. • Bring expertise and support both the architecture and implementation of the standardization of entity and metadata across all data transformations of clinical, molecular, research and imaging data assets. • Lead data42’s efforts improving data interoperability by enhancing the FAIR-ness of the group’s data by working with engineers, curators, architects and data experts. • Architect and support the implementation of solutions to seamlessly exchange metadata with other NVS systems. • In conjunction with a scrum master, run the team through an agile sprint methodology Minimum requirements What you’ll bring to the role • Advanced Degree in Computer Science, Life Sciences or another relevant business discipline • Extensive work experience in knowledge representation, semantic modelling, semantic interoperability, lexical and semantic resources, knowledge engineering and use of text mining technologies from an industrial or academic environment in the biomedical domain • Thorough understanding of problems associated with biomedical, pharmaceutical, genomic/proteomic terminology and data • Sound understanding of scientific terminologies in relevant areas and an in-depth understanding of linked-data concepts and solutions • Knowledge of Ontological authoring & engineering e.g. ontology development process, ontology life cycle, methodologies, tools and languages required for building ontologies. • Web-oriented technologies and programming languages (Java, Perl, Python, XML, HTML, HTML5, JavaScript, CGI, etc.) • Knowledge of Semantic Web Technologies (Web 2.0/3.0, RDF/OWL/SKOS, SPARQL...) and their application to the biomedical domain (OBO) • Knowledge of automated information extraction and text mining techniques, computational linguistic analysis, and their application to scientific textual data, computational lexicons, relational analysis, clustering, and categorization techniques • Proficiency in English (oral and written) Why consider Novartis? 799 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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21.07.2020

Novartis AG

Process and Quality Lead - data42

  • Novartis AG

  • 4051Basel

  • 21.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID298862BRPosition TitleProcess and Quality Lead - data42Apply to Job Job Description Are YOU curious? Are YOU ready to harness advanced data analytics on over 20 years of R&D data and reimagine medicine? We are looking for you! data42 is Novartis’ ground-breaking initiative that harnesses the power of R&D data in one of the largest and most diverse datasets in the pharmaceutical industry to reimagine medicines. data42 applies machine learning, artificial intelligence and sophisticated analytics to generate new insights that increase our understanding of disease and medicines, improves R&D decision-making and ultimately reimagines drug discovery and development. Our Process and Quality Lead with have a significant impact on the quality of data products delivered by data42. You’ll oversee the delivery of high-quality data through well-understood transformational processes that are essential to data42’s efforts. Through the implementation of process and quality controls, you’ll ensure the long-term stability of the data42 program and increase the utility of the products and data we provide. If you have a passion for creating and nurturing process and quality practises and are excited at the prospect of having a positive impact on medicine, why not consider an application today! Flexible locations offered in Basel, Dublin or Cambridge (US). Your responsibilities include, but are not limited to • Overseeing the process documentation and quality control steps of data42’s data operations • Consulting with pipeline owners to improve process quality and throughput, as needed • Designing automated, manual and semi-manual data health-checks into the flow of data from source system to application-ready data assets. Triangulating quality in terms of content, not just completeness • Building, maintaining and managing quality and process metrics within data42’s platform; Engaging with data consumers to ensure that quality meets their needs and expectations. • Building and managing compliance documentation for SOPs and NVS standards on the data process and quality controls • Supporting and maintaining a queue of known or potential quality issues to prioritize and address • Lead the team through an agile sprint methodology in collaboration with our Scrum Master Minimum requirements What you’ll bring to the role • Bachelor’s Degree with an advanced Degree preferred • Solid experience in formulating Data Quality frameworks and delivering Data Quality initiatives in life sciences • Strong knowledge of process mapping, VSM, lean and excellence and/or quality improvement • At least 5 years of working knowledge of and ability to apply Lean and Six-Sigma principals and other similar problem-solving tools (DMAIC, 5Y, Process Mapping, VSM) • Experience with automated quality checking or semi-automated systems • Proficiency in English (oral and written) Desirable Requirements • Ability to manage large quality control operations in data-heavy environments is a plus • Lean Six Sigma certification (e.g., green belt, black belt, master black belt, or other) are advantage • Knowledge of clinical data and/or molecular data is a plus Why consider Novartis? 799 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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21.07.2020

Novartis AG

Patent Attorney - Biology, Research & Development (80-100% )

  • Novartis AG

  • 4051Basel

  • 21.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID280136BRPosition TitlePatent Attorney - Biology, Research & Development (80-100%*)Apply to Job Job Description 30000+ active patent records! And 150+ patent applications filed annually! Are you curious and inspired to reimagine medicine as part of a collaborative and creative team of patent attorneys? Join our global R&D Intellectual Property team spread across 5 sites in the U.S. and Switzerland to make an impact on how we protect innovative medicines for patients WHAT YOU’LL BRING TO THE ROLE: • Provide clear, informed and sophisticated counseling to Novartis R&D clients (e.g., including Novartis Institutes for BioMedical Research (NIBR) and Global Drug Development (GDD) clients) on all IP matters, including opportunities to protect their inventions and to mitigate third party risks • Build and handle patent portfolios for Novartis R&D projects by identifying inventions and preparing, prosecuting, maintaining and defending patent filings for all inventions arising from R&D projects relating to platform technologies, biological targets, new biologic entities, manufacturing processes, and clinical development (e.g., formulations, additional indications, combinations) • Render legal opinions with respect to patentability, validity, and freedom to operate, and formulate patent strategies for Novartis R&D clients that secure IP protection, Freedom-to-Operate (FTO), and enable IP defense(s) • Apply deep expertise in national patent law and practice, including patent trends and case law developments, to devise patent strategies and advice • Understand other forms of protection relating to exclusivity, and applies as required • Build and manage external relationships with outside counsel and collaborators, including substantial interactions within a multicultural global patent function • Provide IP support for transactional projects, such as research collaborations and in-licensing opportunities, including advice on contract drafting and negotiation • Conduct due diligence assessments and counsel based on these assessments, including freedom-to-operate (FTO), infringement and validity analyses, and risk evaluation and mitigation • Direct the R&D Patents Search & Analytics team to provide integrated search support for IP and transactional activities • Effectively communicate with colleagues and leadership in the legal and IP function as well as the R&D organization • Conduct timely review of assigned external publication requests • Continue professional development and contribute to development of IP colleagues *Some restrictions on flexible working options may apply and will be discussed during interview if applicable Minimum requirements EDUCATION Minimum education: B.A., B.Sc. (or equivalent) in Biomedical Sciences or equivalent; Registered European Patent Attorney, preferably also EU-national Patent Attorney Qualification. Desirable education: M.S., Ph.D. or equivalent in Biomedical Sciences EXPERIENCE: At least 3 year experience as a Qualified European Patent Attorney in a law firm or in the research and development industry with significant responsibility for patent prosecution and counselling, including patent drafting and prosecution in the biotechnology industry. KEY CAPABILITIES • Strong scientific background in biological sciences; preferably including direct lab experience • Expertise in local (US or EP) and PCT law, filing process and prosecution practice; detailed understanding of counterpart EP or US law and other major global patent systems • Strong customer-service focus to build and sustain effective partnerships with key stakeholders and project teams • Effective analytical, presentation and communication skills • Proven ability to work independently as well as collaboratively in a team • Well-developed research and critical thinking skills, and sound decision-making abilities, with attention to detail to produce consistently accurate work • Strong organization and time management skills with flexibility, creativity, resourcefulness to successfully prioritize and manage multiple, competing priorities simultaneously • Interpersonal skills (partnership, influence/persuasion, teamwork) • Ability to incorporate global outlook and management of product life-cycle into decision-making process WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

20.07.2020

Novartis AG

Senior Manager Group Financial Reporting and Accounting

  • Novartis AG

  • 4051Basel

  • 20.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID299236BRPosition TitleSenior Manager Group Financial Reporting and AccountingApply to Job Job Description This position will interpret and implement IFRS accounting standards within the Novartis Group, in particular in the area of taxes, ensuring that policies and procedures as well as effective financial controls are in place to provide the Group with high quality, compliant accounting standards advice and documentation, respecting the Novartis Accounting Manual (NAM), IFRS, Swiss, US and other regulatory requirements. Your responsibilities will include: - Functional technical accounting lead in reporting of SOX compliant, current and de-ferred income taxes including tax rate analysis and providing high quality, compliant and efficient support of the business, and tax content for external reporting and related SOX controls. - Timely preparation of tax rate forecasts for the purpose of Target, Latest Forecasts, Stra-tegic plan and the quarterly closings together with Group Tax and presentation of pro-posals to Senior Management - Provide accounting and reporting guidance on the tax impact of complex transactions, including M&A, contracts, internal reorganizations and business development and licens-ing transactions in collaboration with other relevant departments to ensure compliance with IFRS accounting and reporting requirements. - Assess implications of upcoming changes in IFRS for the financial statements of Novartis and collaborate within Novartis, with industry contacts and auditors, in interpreting and implementing new accounting standards, providing thought leadership in designing and implementing new reporting requirements. - Manage tax related requests and recommend NAM revisions, ensuring the NAM remains up-to-date and aligned to /consistent with IFRS and Novartis accounting principles and guidelines. - Make presentations and train associates on Group, divisional and regional level on financial reporting and technical accounting Minimum requirements What you’ll bring to the role: - University Degree in finance/accounting/economics or MBA; Certified Public Accountant/Chartered Accountant with in-depth IFRS knowledge - Excellent English both spoken and written. German or other European language will be a plus - Relevant work experience in finance of 6 to 8 years with a multinational and/or Audit experience with a major (i.e. Big 4) public accounting firm. - Experience in reporting of current and deferred taxes - Strong technical accounting competence acquired in: Auditing: minimum 3-5 years in major auditing company, and 2-3 years in a multinational financial reporting environment or senior technical specialist in major international company using IFRS or US GAAP - Management experience working within a matrix, functional leadership responsibility - Good SAP ERP understanding a plus - Good understanding of the Healthcare industry WHY CONSIDER NOVARTIS? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis!DivisionCORPORATEBusiness UnitGlobal Corp. FinanceLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaAudit & FinanceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

19.07.2020

Novartis AG

Associate Director, RWE and Data Science, China (80-100% )

  • Novartis AG

  • 4051Basel

  • 19.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID299169BRPosition TitleAssociate Director, RWE and Data Science, China (80-100%*)Apply to Job Job Description >500 Million real world patient records are used to help reimagine how integrated evidence generation will transform healthcare decision making. You will provide methodological and analytical expertise, provide strategic input regarding utilization of real world evidence (RWE) in China; and provide leadership of real world Chinese database analyses. Your responsibilities will include: • Serve as analytical expert on real world evidence generation methods and analytic projects for China aligned with local and Global priorities. • Provide expert consultation on analytical issues including, but not limited to exploratory analyses from real world databases, and the conduct of full non-interventional studies. • Ensure latest methodologies and breakthrough analytical technologies are implemented for RWE projects in China. • Provide expert input into the development of the real world evidence plans in close collaboration with the China GDD, China HEOR/access, China Medical Affairs, and other relevant stakeholders in priority disease areas. • Interpret findings from non-interventional data analytic projects, and communicate key insights and messages to various cross-functional teams and externally via publications and presentations. • Provide critical scientific review of all China RWE protocols. Minimum requirements What you’ll bring to the role: • 5+ years conducting RWE research for pharmaceutical products in the pharma industry, contract research organization, or academic institute; or experience in a closely related discipline within the pharma industry (e.g., clinical research, statistics, epidemiology, pricing) • Deep understanding of RWE study methods; thorough understanding of study designs that provide most relevant evidence to decision-makers • Deep understanding of available and emerging RWD data sources, particularly in China. • Demonstrated research accomplishments including publications,, and presentations at scientific conferences • Strong collaboration and networking skills to foster productive internal relationships cross-functionally • Fluent oral and written English and Mandarin Chinese *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionPHARMABusiness UnitGLOBAL MEDICAL AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarket AccessJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

19.07.2020

Novartis AG

Executive Director, Global Omni-channel Strategy

  • Novartis AG

  • 4040Basel

  • 19.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID297258BRPosition TitleExecutive Director, Global Omni-channel StrategyApply to Job Job Description 1400! That is how many marketers you will collaborate with. Global Marketing Innovation and Execution owns the marketing functional mandate within Novartis Pharma and is responsible for enabling Marketing transformation across 1400 marketers to ensure best in class execution within an evolving digital landscape. You will be part of the Global Marketing Innovation and Execution team, which sits within the Global Marketing organization. This new team, created in 2019, has the remit to drive marketing transformation across three critical strategic ‘pillars’ (1) Building Novartis brands, which better connect with customers and have sustainable brand equity (2) Embedding strong & future proofed core capabilities (platforms, process, skills, working models) for our 1400 pharma marketers (3) Accelerating the transition towards of Omni channel and Customer Experience marketing with one centrally led and executed strategy. Our purpose is to create a sustainable competitive advantage that energizes and focuses our organisation to deliver tangible business results versus competitors, whilst improving lives of our patients. Your focus will be t our pillar 3: focusing on transforming digital/omnichannel marketing within Novartis. Your responsibilities: • Foster cross-franchise, cross-region and cross functional communication and best practices sharing in multichannel marketing. • Liaises with Global Franchises, Regions and CPOs to clarify customer needs and undertakes an environmental scan of the digital landscape to understand patient and healthcare stakeholder needs as well as being fully aware of competitor landscape • Ensure that team keep closely tracks emerging and evolving digital technologies and new channels for the Healthcare & Pharma Industries. Leveraging proof of concept to test ideas, concepts and channels. • Customer Acquisition Strategy: Demand Generation and Channel Mix Optimi-zation • Customer-Centric Content Distribution Strategy: • Transformational leadership Minimum requirements What you’ll bring to the role: • Bachelor’s required. MBA preferred • English (Oral and Written) • Minimum 7-10 years of digital experience related to commercial and medical activities, including implementing and scaling digital solutions • Experience in driving digital Global change management in large organizations with senior facing responsibilities, in pharmaceuticals or other industries • Demonstrated business impact of multichannel initiatives, through organizational metrics, revenue, profit or cost-cutting initiatives. • Recognized standing in the Global multichannel and digital marketing arena with a track record of innovation • Solid understanding of Global digital landscape, development processes and methodolo-gies, demonstrated innovative mindset • Firm grasp of the regulatory environment in marketing to HCPs Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

19.07.2020

Novartis AG

Senior Manager Internal Audit EMEA

  • Novartis AG

  • 4040Basel

  • 19.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID293264BRPosition TitleSenior Manager Internal Audit EMEAApply to Job Job Description We are looking for a (Senior) Internal Auditor in the EMEA (Europe, Middle East and Africa) team to be a trusted partner who keeps Novartis’ patients, associates, customers, assets, and reputation safe, and who helps Novartis be successful in reimagining medicine. 105,000 unique individuals work at Novartis, all with different needs and aspirations, aligned to a single inspirational purpose; to Reimagine Medicine for millions of patients around the world. You will have opportunities to help improving governance, risk management, processes and our culture, and to engage with senior leaders of Novartis Corporate functions and country organizations. You will also be able to further develop your skills and strengths that will help you to reach new heights and to find professional fulfillment in an inspired, curious and unbossed organization. You will be responsible but not limited to: • Plan, deliver and follow up from assurance and advisory projects in the EMEA markets and at the corporate level either as a team lead or team member. • Identify the root causes of audit findings and investigate, analyze and recommend practical solutions to prevent re-occurrence. • Act as a cultural change agent who supports the creation of an inspired, curious and unbossed organization. • Support the EMEA audit team by providing peer-to-peer coaching and training, as well as, on-boarding new team members. • Manage knowledge and drive innovation to ensure high-quality, value-adding and digitally enabled audit execution. • Contribute to the digital transformation of the audit function to leverage the opportunities presented by current and new technologies and data across the organizations. • Contribute to or lead regional or global Internal Audit methodology projects and continuous improvement initiatives. Minimum requirements • Postgraduate degree preferably in business administration (accounting, finance, economics, marketing) • Fluent in English, at least one other language desirable, like Russian, French, German, Spanish, or any EMEA language • 4 to 8 years of relevant working experience in internal audit/advisory departments in a big four, in an IA boutique or consulting firm with focus on Pharma or the healthcare sector • OR 4-8 years of working experience in an internal audit department of an international company preferably in Pharma, medical devices, or Biotech sector • OR a minimum of 10 years of experience in the business (e.g. commercial, general management, Finance) with a strong interest in internal audit • Good knowledge of SAP FI and CO modules, ACL, Tableau, or other audit tool • 40% travel is required for this role Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionCORPORATEBusiness UnitBUSINESS ASSURANCE AND ADVISORYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaAudit & FinanceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.07.2020

Novartis AG

Internship Inclusion & People Engagement Switzerland

  • Novartis AG

  • 4040Basel

  • 17.07.2020

  • Praktikumsstelle

Back to Previous Page Job ID299145BRPosition TitleInternship Inclusion & People Engagement SwitzerlandApply to Job Job Description The Inclusion & People Engagement Switzerland Team is offering a one-year internship for a highly motivated bachelor graduate. Your responsibilities: Your responsibilities include, but are not limited to: • Support the implementation of the Inclusion & People Engagement Switzerland Communications plan including o writing and editing of short articles for Basel News & Yammer o uploading content to the appropriate channels with the corresponding tools, e.g. CCM o tracking of ongoing and planned communication activities o maintenance and further development of SharePoint and Intranet presence o update internet with Inclusion & People Engagement topics and initiatives o support the development of other communications materials, e.g. videos o creation of standard presentation as well as supporting team members in preparing presentations for their projects • Organization and preparation of Inclusion & People Engagement events and activities, e.g. curiosity month activities • Support the event management of Inclusion & People Engagement events like ‘Understanding the Swiss education system event’, including o creation of communication materials (banners, invitations, leaflets) o organization of infrastructure (technical, location, catering) o coordination of activities with all relevant stakeholders • Collaboration with relevant internal and external stakeholders, e.g. Communications Switzerland, IT, third party agencies, ERGs • Ensuring brand compliance of all communications materials Minimum requirements What you'll bring to the role: • Recent Bachelor graduate (graduation not longer than one year ago) in communications or related area • Proficiency in English and German (written and spoken) is a must • Good communication skills including writing and editing • Structured personality with excellent organizational skills • Good knowledge of MS Office tools, including SharePoint •Open and collaborative personality with good interpersonal skills Start date: December 1, 2020 Duration: 1 year Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionNBSBusiness UnitHR NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

16.07.2020

Novartis AG

Head of HSE, Switzerland - Novartis HQ (Executive Director)

  • Novartis AG

  • 4051Basel

  • 16.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID298998BRPosition TitleHead of HSE, Switzerland - Novartis HQ (Executive Director)Apply to Job Job Description 108,000! That’s the number of associates whose lives HSE touches and improves. Join us in our mission to protect our people, patients and planet as part of the Novartis Health, Safety and Environment team. Reporting to the Global Head HSE, you are responsible for significant HSE programs in the Novartis Global HQ country, with high visibility to and contact with senior Novartis leadership and Swiss & French Governmental Authorities. Yours is a leadership position with direct impact on the success of HSE at Novartis in Switzerland and globally, and the business owning HSE performance and risks. Your key responsibilities • Lead the Switzerland HSE organization (~13 plus third parties), defining the HSE strategy, roadmap and end-state design options in line with the Global HSE vision for mixed workplace environments. These include scientific disease research labs, offices and sophisticated manufacturing / production sites for approximately 12,200 employees. • Member of the Global HSE Leadership Team (6 members): partnering with peers on global HSE strategy, and with subject matter experts from across different regional teams to ensure innovative solutions achieved for Switzerland have global relevance • Representing HSE at the Switzerland Real Estate and Facilities Services Leadership Team, and the Site Management Board, delivering expert advice and support to the business needs of clients • Accountable for the strategy and operations for Health & Safety, and leading operations for environmental compliance. Partnering with our integrated provider CBRE, setting clear objectives, leading performance reviews, ensuring effective governance throughout Novartis for all Switzerland sites, and preparing budgets in line with business plans. Your overall budget ~CHF 5.5m p.a. • Providing direct people management and operational management supervision to site-based HSE Officers and their teams across Switzerland, you will also oversee third-party CBRE personnel and other contractors providing services to Novartis. COVID-19 has accelerated the significance of the wide range of strategic Novartis HSE change programs already underway globally and in Switzerland, including moving from defined technical procedures and regulations towards a people-focused approach enabling employees to take care of their HSE, and opening the HQ Campus in Basel to external companies for integrated innovation. The health & safety of our employees is of primary importance and your expertise towards workplace safety is significant towards this. Minimum requirements What you’ll bring to the role • University degree in safety engineering, safety management, industrial hygiene, environmental science, occupational health and/or medicine, engineering, or related field: Master’s degree or higher preferred. • Multi-lingual: Business-level (C1, C2, fluent) English and German. Additional advanced French strongly preferred. Italian advantageous. • Significant (i.e. 15 years+) relevant work experience within multi-national organizations, including at least 10 years in a leadership / people manager responsible for multi-site mixed environment HSE strategy & operations. You have very strong people, program, business leadership and senior stakeholder management experience from leading multiple high impact programs and processes that delivered credible HSE improvements across global/regional, cross-functional, matrix organizations. Previous experience leading a region is strongly preferred • Good knowledge of modern HSE tools, systems and processes • You communicate effectively across organizations with a high level of personal credibility, customer relationship management, and networking: successfully identifying and managing diverse stakeholders thanks to your superior interpersonal / influencing skills. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network: https://talentnetwork.novartis.com/networkDivisionNBSBusiness UnitREFS NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaFacilities & AdministrationJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

16.07.2020

Novartis AG

Head Legal NTO Transactions

  • Novartis AG

  • 4051Basel

  • 16.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID298817BRPosition TitleHead Legal NTO TransactionsApply to Job Job Description 70+ billion! That’s the number of units Novartis Technical Operations (NTO) supplied to over 150 countries in 2019. Our 26,000+ associates from 100 different countries are working hard to build an inspired, curious and unbossed culture in which everyone is enabled to be their best. We are unleashing the power of our people and putting data and digital at the heart of a transformation that is enabling us to reach more patients, more quickly, all across the world. To support the Novartis aspiration of becoming the leading medicines company in the world, we are re-imagining manufacturing, aligning our capacity and capabilities with the changing needs of the Novartis portfolio. As our evolution continues, we are proud to provide the manufacturing technology on which many of our innovative new treatments rely and to be the organization that provides our patients with the medicines they need to live longer, healthier lives. As our Head Legal NTO Transactions, you will support the General Counsel NTO & Group Quality NTO in any strategic projects. Leading a team of two Senior Legal Counsel associates and acting as the head lawyer for NTO, in assigned global transactions / projects in the area of Network Transformation, M&A and BD&L; ensure strategic legal advice, robust risk assessment, and effective and efficient legal support during all stages of the relevant transactions / projects, in accordance with NTO strategy, and in compliance with all relevant laws and regulations. Your responsibilities will include: • Be a member of the NTO Legal LT, supports the General Counsel NTO & Gp Quality in strategic projects and actively contributes to the design and execution of the Function’s strategy. • Acts as a pro-active, business-minded legal partner to the Network Transformation, M&A and/or BD&L NTO global support teams during planning, negotiation, execution and implementation of the relevant transactions / projects. Ensures the execution of projects in accordance with the project plan, NTO strategy and in compliance with all relevant laws and regulations. • Represents NTO L&C as lead lawyer in all assigned projects in the area of Network Transformation (Expansion, closing, divesting of sites / outsourcing of manufacturing), M&A and/or BD&L (acquisition, divestment, in- or out-licensing), and, as required, prepares / conducts due diligences, drafts, negotiates and reviews all related agreements, and any related internal or external communication to management, employees, authorities, interested parties (bidders), suppliers or any other third party. • Is an acknowledged expert resource for the entire NTO function in their field, and plays a key coordination role for all relevant legal and other functional experts’ input to any transaction or implementation documentation. • Manages and works with outside counsel and, when and as necessary, closely monitors and controls related legal spend. • Manages potential disputes and dispute resolution relating to the assigned transactions / projects. • Supports the establishment, design and implementation of clear guidelines and processes to provide optimal and timely NTO legal support for transactions / projects, while ensuring their execution and implementation in accordance with NTO strategy and in compliance with all relevant laws and regulations. • Advises and determines appropriate actions regarding legal and compliance issues in relation to transactions / projects, including the training of lawyers and clients. Minimum requirements What you’ll bring to the role: • Law School Graduate & Bar member. Additional qualifications in related fields (e.g. finance, tax, regulatory, etc.) are a plus. • Acknowledged as an expert and a resource for the legal function in the manufacturing, regulatory and transactional field with the ability to: analyze complex legal issues; lead contract negotiations of several complex projects independently; and play a key coordination role with lawyers and other functional experts, and having a minimum of: • 8 years post-Bar experience, ideally gained within a healthcare / pharmaceutical environment or, alternatively, with a top-tier law firm representing healthcare clients, of which, 5 years of that experience was in leading complex legal transactions, restructuring and outsourcing projects. • Able to set priorities and to lead a wide-ranging workload under time and organizational pressure, often involving multiple projects simultaneously. • Excellent team player with strong verbal and written communication skills. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionNovartis Technical OperationsBusiness UnitNTO LEGALLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

15.07.2020

Novartis AG

Internship - Public Affairs Europe & Global Business Franchises

  • Novartis AG

  • 4051Basel

  • 15.07.2020

  • Praktikumsstelle

Back to Previous Page Job ID298997BRPosition TitleInternship - Public Affairs Europe & Global Business FranchisesApply to Job Job Description 750 million lives touched by our products. Imagine what you could do at Novartis. No matter where you work, you could contribute to solving some of the toughest healthcare challenges and have an extraordinary impact on people’s lives. Join us. The Novartis Intern Public Affairs (PA) Europe team is looking for a motivated intern, who can support in analysis, meeting preparation and projects. One of the key Public Affairs responsibilities is to enable Novartis to be a leading government partner, committed to improving and extending patients’ lives and enhancing access to science-based innovation. We also foster long-term relationships with stakeholders on a local and above-country level and deliver key messages on Novartis’ commitments. Your responsibilities: Your responsibilities include, but are not limited to: • Coordinate inputs for senior management documentation and meetings as needed • Provide tailored information to management, countries & Business Units on external developments as appropriate; provide briefings and support • Maintain distribution lists and fact sheets • Offsite execution • Conduct data analysis for the Public Affairs Europe Team • Execute small independent projects related to government affairs strategies • Support maintenance of Public Affairs Europe community • Support execution of capability building program • Meeting organization as well as follow up, presentation preparation • Contribute to ongoing projects on PA strategies as well as analytics reports • Support the activities of Global Public Affairs Franchise team in coordination with key countries and regions Minimum requirements What you’ll bring to the role: • Recent Master graduate in Public Health, Public Policy or Political Science (graduation not longer than one year ago) • Fluent English (written & spoken), additional European language is a plus • Working experience in a related function, e.g. public affairs, corporate strategy, management consulting or equivalent, with exposure to healthcare issues. • Project management skills; ability to executive projects across divisions, business units and functions. • Knowledge of European healthcare systems Timing: September 1, 2020 Duration: 6-9 months Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionCORPORATEBusiness UnitNOVARTIS CORPORATE AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

14.07.2020

Novartis AG

Global Program Safety Lead, Cardio Renal Metabolic (80 - 100% )

  • Novartis AG

  • 4051Basel

  • 14.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID298550BRPosition TitleGlobal Program Safety Lead, Cardio Renal Metabolic (80 - 100%*)Apply to Job Job Description 1,430,000! This is how many patients with Heart Failure we have treated! Our Cardio-Renal-Metabolic Development Unit is making courageous choices to develop treatments to transform lives. We are committed to reduce the global burden of Heart Failure, Atherosclerosis, Renal diseases and Metabolic disorders on patients, families, and communities. As a Global Program Safety Leader, you will ensure that we safely offer transformative treatments for Heart Failure patients and will design and develop safety surveillance strategy for products and approval. You will be responsible for the company’s drug surveillance program including the necessary follow-up and risk assessment in addition to adverse reaction reports, oversight of safety in clinical trials and post marketing programs. You will participate in the resolution of any legal liability and comply with governmental regulations. In addition, you will provide and contribute trending and safety signal detection and risk management assessment for the products’ life cycle and provide safety support to the clinical development teams. Your responsibilities will include: • Providing expert safety input to the clinical development program for assigned projects/products and being an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT) • Safety issue management from formation of Global Program Team (GPT) through Life Cycle Management. • Development and responsibility for key internal Novartis safety documents: reviewing these documents regularly and updating as required • Responsibility for overall signal detection, monitoring, evaluation, interpretation and appropriate management of safety information, based on information from all relevant line functions, post-marketing data, and other sources. • The initial development and ongoing maintenance of safety information in Core Data Sheet (core global labeling), including addressing safety issues optimally in all project/product labeling indications. • Responsibility for responses to inquiries from regulatory authorities or health care professionals on safety issues • Leading the preparation of the safety strategy for health authority responses and strategy, in collaboration with other project team members. Minimum requirements What you’ll bring to the role: • Medical Degree or equivalent (preferred), PhD, PharmD or equivalent graduate level health care professional degree required. • Fluent in spoken and written English • 3 years clinical experience postdoctoral • At least 5 years experience of drug development in a major pharmaceutical company (of which 2 years in a global position), including 2 years in safety at an operational or medical position • Experience in preparing or contributing to preparation of clinical safety assessments and regulatory reports/ submissions involving safety information • Prior experience of leading cross-functional, multi-cultural teams • Experience with (safety or others) issue management, drug development, clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications Desirable: • Specialty Board certification *Some restrictions on flexible working models may apply and will be discussed at interview if relevant Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitCMO & PATIENT SAFETY GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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14.07.2020

Novartis AG

Senior Quantitative Safety Statistician (80-100% )

  • Novartis AG

  • 4051Basel

  • 14.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID296303BRPosition TitleSenior Quantitative Safety Statistician (80-100%*)Apply to Job Job Description 1 in 10,000 is the frequency of a rare safety event! The science of detecting, quantifying and communicating adverse drug reactions as well as designing measurable risk minimization activities – this is quantitative safety science. Providing patients with more benefits than risks is Novartis top priority. As Senior Quantitative Safety Statistician you will shape the quantitative safety strategy of a drug during the whole life cycle. RESPONSIBILITIES WILL INCLUDE BUT ARE NOT LIMITED TO: • Owning the implementation of innovative quantitative methods to evaluate the safety and benefit-risk profile of a drug based on data from multiple sources • Providing strategic direction and statistical expertise to collection, evaluation and presentation of safety data ensuring a holistic, efficient and consistent approach • Coordinating quantitative safety activities to answer requests from health authorities • Providing statistical expertise and oversight to non-interventional studies • Proposing and implementing innovative and process improvement initiatives related to quantitative safety. * Some restrictions may apply on flexible working and will be discussed at interview it applicable Minimum requirements WHAT YOU’LL BRING TO THE ROLE: • University degree in statistics or mathematics or related area (PhD preferred) • Proficiency in English • 6+ years of experience in positions with growing responsibility in the Pharmaceutical Industry; with 4+ years applying statistical methods to drug development and post-marketing safety • Demonstrated experience in developing and evaluating modern quantitative safety methodologies. Computing ability and experience with different data sources. • Demonstrated contribution to external white-papers/policy shaping best practice in statistical science and experience in leading scientific improvement/ change initiatives • Scientific curiosity combined with strong communication skills bridging scientific and business needs over different expertise areas • Excellent strategic skills. Natural leadership style with the ability to build successful partnerships at all levels Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitCMO & PATIENT SAFETY GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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14.07.2020

Novartis AG

USP Senior Scientist in Viral Vectors Development

  • Novartis AG

  • 4051Basel

  • 14.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID296448BRPosition TitleUSP Senior Scientist in Viral Vectors DevelopmentApply to Job Job Description 160+ projects in clinical development. And that’s just in 2019. This is your chance to help reimagine medicine in 2020! We are looking for a highly motivated Senior Scientist for the Viral Vectors Development Team, Cell and Gene Technical Development that is responsible for the development of viral vectors upstream and downstream manufacturing processes and drug products. The candidate will be accountable for viral vectors upstream process (USP) aspects with special focus on Lentiviral Vector based Cell and Gene Therapies. As Senior Scientist, you will lead the design, the planification and the execution of cell culture experiments to develop efficient production processes. You will evaluate new technologies to increase cell culture process understanding and processes performance. Your scientific responsibilities will include the reporting of scientific experiments for the preparation and timely delivery of drug substances (DS), and the transfer of upstream processes to GMP facilities. Within the CGT field, the candidate will bring expertise in Lentiviral Vector process development and manufacturing with focus on upstream technologies. Main responsibilities • Design, plan, perform and document scientific experiments to contribute to project related scientific/technical activities (e.g., interpret and report results, generate and evaluate data, draw relevant conclusions, write reports). • Provide efficient and robust upstream processes for the manufacture of DS. Lead the scaling-up of process with a deep characterization of critical process parameters. • Generate scientific documents to hand over to internal and/or external partners (e.g., TechOps, authorities, external companies) and support generation of international registration documents under adequate guidance from more experienced team members. • Utilize special tools/equipment as an expert. Work closely with suppliers to evaluate new technologies and improve productivity. • Coordinate USP activities and give guidance to team members according to appropriate SOP’s, GLP, HSE and Novartis guidelines. Minimum requirements • Relevant Bachelor's / Master's degree in Cell Culture, Bioprocessing, Bioengineering or equivalent with 3-5 years experience in upstream processing of Lentiviral Vectors and/or viruses in an industrial environment or PhD with experience in USP of Lentiviral Vectors in industrial environment. • Strong understanding of mammalian cell culture processes (thaw to production) in viral vectors production. • Several years of hands-on experience with suspension cells, different scales of bioreactors, and viral production in Biosafety regulation BL-2. • Experience in supporting multidisciplinary project teams. • Good knowledge of English (oral and written). Desirable Requirements • Familiarity with GMP requirements. • Ability to mentor junior level staff. WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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13.07.2020

Novartis AG

External Innovative Partnership Head Cardio Renal Metabolic (80-100%)

  • Novartis AG

  • 4051Basel

  • 13.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID298401BRPosition TitleExternal Innovative Partnership Head Cardio Renal Metabolic (80-100%)Apply to Job Job Description 3000! That is the number of medical associates worldwide who will benefit from your work. As External Innovative Partnership Head, you will develop and lead global strategic partnerships for the Cardio Renal Metabolic franchise in collaboration with cross-functional colleagues. Partnerships of strategic importance are intended to change or advance the clinical practice in disease areas relevant to the franchise, and are intended to improve patient outcomes and access to the right treatments at the right time. Relevant partnerships will include a wide variety of external stakeholders, such as professional societies, academic institutions, HTA bodies, other pharma companies and start-up companies Your responsibilities will include: • Build a strong network with key professional societies, patient organizations, insurers, payers, governments, health systems and start-up companies. • Identify key partnership opportunities for research or educational purposes. • Build a deep understanding of key health systems across the globe, and identify key needs and opportunities to improve clinical care and outcomes for patients with diseases included in the franchise. This may include (new ways of) evidence generation, education of clinical practioners, developing new relevant clinical endpoints, developing new clinical evaluation and/or management tools, etc. • Align within the franchise on key opportunities to improve clinical care and patient outcomes, and identify possible external partners/bodies who have aligned objectives and have an interest in collaboration. • Develop framework to support the identification, funding framework, evaluation of rigor and fit, engagement and development of strategic partnerships and technologies according to their fit to the business and priorities. Minimum requirements What you’ll bring to the role: • 8-10+ years relevant pharma experience acquired at pharmaceutical companies, especially good understanding of the franchise disease area. • Ability to quickly establish credibility, influence and respect, set clear and ambitious goals, lead strategic analysis and innovation, and inspire collaboration from peers and stakeholders. • Strong organizational, interpersonal and influencing skills. Ability to probe, challenge and question appropriately and strive for continual improvement • Deep understanding healthcare ecosystem and Pharmaceutical industry interfaces • Strong understanding of drug development with proven ability to identify and deliver key evidence needs a diverse range of stakeholders. • Deep understanding of pharmaceutical value chain and its business processes, strong knowledge of clinical and real-world data Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionPHARMABusiness UnitGLOBAL MEDICAL AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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13.07.2020

Novartis AG

External Innovative Partnership Head Neuroscience (80-100%)

  • Novartis AG

  • 4040Basel

  • 13.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID298285BRPosition TitleExternal Innovative Partnership Head Neuroscience (80-100%)Apply to Job Job Description 3000! That is the number of medical associates worldwide who will benefit from your work. As External Innovative Partnership Head, you will develop and lead global strategic partnerships for the Neuroscience franchise in collaboration with cross-functional colleagues. Partnerships of strategic importance are intended to change or advance the clinical practice in disease areas relevant to the franchise, and are intended to improve patient outcomes and access to the right treatments at the right time. Relevant partnerships will include a wide variety of external stakeholders, such as professional societies, academic institutions, HTA bodies, other pharma companies and start-up companies Your responsibilities will include: • Build a strong network with key professional societies, patient organizations, insurers, payers, governments, health systems and start-up companies. • Identify key partnership opportunities for research or educational purposes. • Build a deep understanding of key health systems across the globe, and identify key needs and opportunities to improve clinical care and outcomes for patients with diseases included in the franchise. This may include (new ways of) evidence generation, education of clinical practioners, developing new relevant clinical endpoints, developing new clinical evaluation and/or management tools, etc. • Align within the franchise on key opportunities to improve clinical care and patient outcomes, and identify possible external partners/bodies who have aligned objectives and have an interest in collaboration. • Develop framework to support the identification, funding framework, evaluation of rigor and fit, engagement and development of strategic partnerships and technologies according to their fit to the business and priorities. Minimum requirements What you’ll bring to the role: • 8-10+ years relevant pharma experience acquired at pharmaceutical companies, especially good understanding of the franchise disease area. • Ability to quickly establish credibility, influence and respect, set clear and ambitious goals, lead strategic analysis and innovation, and inspire collaboration from peers and stakeholders. • Strong organizational, interpersonal and influencing skills. Ability to probe, challenge and question appropriately and strive for continual improvement • Deep understanding healthcare ecosystem and Pharmaceutical industry interfaces • Strong understanding of drug development with proven ability to identify and deliver key evidence needs a diverse range of stakeholders. • Deep understanding of pharmaceutical value chain and its business processes, strong knowledge of clinical and real-world data Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionPHARMABusiness UnitGLOBAL MEDICAL AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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13.07.2020

Novartis AG

Scientific Lead - data42

  • Novartis AG

  • 4040Basel

  • 13.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID296430BRPosition TitleScientific Lead - data42Apply to Job Job Description Are YOU curious? Are YOU ready to harness advanced data analytics on over 20 years of R&D data and reimagine medicine? We are looking for you! data42 is Novartis’ groundbreaking initiative that harnesses the power of R&D data in one of the largest and most diverse datasets in the pharmaceutical industry to reimagine medicines. data42 applies machine learning, artificial intelligence and sophisticated analytics to generate new insights that increase our understanding of disease and medicines, improves R&D decision-making and ultimately reimagines drug discovery and development. Our data42 Scientific Lead will be a core member of data42 product teams supporting the program scientific leadership and helping set key scientific and research priorities aligned with the Novartis mission and goals. You will be our storyteller, harmonising each aspect of the teams’ message from clinical to technology. During the development of the product, our Scientific Lead will guide the development team on research methodologies, scientific accuracy and be the point of contact with the business leads. Our Scientific Lead will also support the Novartis medical and scientific community on how to ask the right questions when using integrated data for clinical and research applications. Your responsibilities include, but are not limited to • Ensuring the scientific value of products developed within data42 • Developing the data42 strategic research roadmap • Supporting our medical and scientific community to ask the right questions • Acting as a scientific advisor to the data42 cross-functional teams • Evaluating potential internal and external scientific partnerships • Storytelling through our digital technology, simplifying our content and helping us to explain it • Being directly responsible for at least one Agile feature team (7-9 people) Minimum requirements What you’ll bring to the role • Higher degree in Life Sciences, Pharmacy, or Medicine (PharmD, PhD or MD), or equivalent • 10+ years life science or healthcare experience • Solid scientific background, a depth and breadth of analysing medical data • 5+ years in the pharmaceutical industry with demonstrated ability to leverage data and analytics for decision making • Strong customer-focused approach and track record of working in complex matrix organizations • Deep understanding of analytics landscape in the Pharma/biotech industry • Effective project and resource management; proven ability to handle a broad range of customers and team members • Ability to be a storyteller, disseminating complex information to a wide audience • Fluent in English (oral and written) Desirable requirements • Omics – Previously worked with big data with an ability to derive data insights • Clinical – Knowledge of clinical trials, from protocols to outcomes • Knowledge of SQL and Python, R or related technologies • Experience with Agile methodologies and Scrum Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous, and collaborative people like you are brought together in an inspiring environment, where you’re given opportunities to explore the power of digital and data. We are Novartis. Join us and help us reimagine medicine. Commitment to Diversity & Inclusion Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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13.07.2020

Novartis AG

Academy in Clinical Sciences & Innovation

  • Novartis AG

  • 4051Basel

  • 13.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID294923BRPosition TitleAcademy in Clinical Sciences & InnovationApply to Job Job Description 2 years! This is the length of our training program within Novartis Institutes for BioMedical Research Clinical Sciences & Innovation (CS&I), which offers training and experience for dedicated fellows who want to develop their career into Clinical Research Operations. Your responsibilities: Through the CS&I Academy, Novartis offers a unique opportunity to step into the field of Clinical Research Operations and gain insight and experience across the many aspects of designing, initiating and running early clinical trials within an international multi-cultural Pharmaceutical research environment. You will develop your current skills and grow professionally: you will be trained by clinical operations experts and have the chance to apply your knowledge and strengths in various project assignments across different disease areas and types of clinical trial work. In parallel to your Academy learning, your core responsibility will be to contribute and support various CS&I teams working on clinical trials as part of the team. Are you excited about the importance of clinical trials and contributing to our mission to reimagine medicine? This program is for you. During the Academy you will... (but not limited to...) • Be trained & onboarded by experts • Embark on a progressive, blended and flexible learning journey covering conceptual, theoretical and experiential modalities • Gain hands-on experience by contributing to and supporting a range of clinical operations work Tasks • Broaden your professional horizon by rotating through a number of different CS&I teams aligned with your interests and based on open opportunities, such as Clinical Trial Team Leads, Finance, Feasibility, Data Sciences and others Minimum requirements What you’ll bring to the role: • A recent (within past 2 years) degree (BA, BSc, MSc, PharmD or PhD), Life Sciences preferred • Fluent English, written and spoken, additional language is a plus • Good organizational and interpersonal skills • Ability to work in a team and independently, managing multiple priorities with support • Computer literate • Interest in clinical research Duration of program: 24 months Application: Please submit your CV and motivation letter under www.novartis.com/careers, JOB ID 294923BR (application period open 13.07.20 to 10.08.20) Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionNIBRBusiness UnitTranslational MedicineLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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13.07.2020

Novartis AG

Pipeline Owner (Clinical Data) - data42

  • Novartis AG

  • 4051Basel

  • 13.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID296427BRPosition TitlePipeline Owner (Clinical Data) - data42Apply to Job Job Description Are YOU curious? Are YOU ready to pioneer AI and ML to harness the power of R&D data to advance science? We are looking for you! 2 million patient-years of data! data42 is Novartis’ ground-breaking initiative that harnesses the power of R&D data in one of the largest and most diverse datasets in the pharmaceutical industry, we will re-imagine medicine. data42 applies machine learning, artificial intelligence and sophisticated analytics to generate new insights that increase our understanding of disease and medicines, improves R&D decision-making and ultimately reimagines drug discovery and development. Our Pipeline Owner will craft and operate industry-scale clinical data pipelines that will ingest, harmonize, unify, anonymize and annotate thousands of clinical trials that are core to data42’s mission. Flexible locations offered in Basel, Dublin or Cambridge (US). Your responsibilities include, but are not limited to • This role would be responsible for overseeing (A) clinical data unification efforts and (B) the accurate ingestion and analysis of data pertaining to pools, (C) support anonymization activities (D) implementation of semantics and metadata standards set for the enterprise (E) Quality and process excellence • Work with technical specialists and operational teams to plan and deliver on data42s ambitions with clinical data assets • Oversee the operations of the end-to-end data pipelines supporting the delivery of high-value clinical data • Determine and develop the maximally flexible architecture needed to serve both core and non-core use-cases of the clinical data asset • Support the team’s approach to semantic which ensures data and metadata standards are met • Implement and support the FAIR principles through the data pipelines created and operated within this role • Lead all aspects of data unification and anonymization efforts and collaborating teams • Build and oversee the teams’ efforts to utilize clinical data pools whenever possible • Support documentation creation of data processed through clinical data pipelines • Be responsive to new needs raised by use-case owners and other ‘customers’ of data42 • Collaborate with governance bodies and data strategy roles to ensure alignment of activities and areas of focus • Support the implementation of key data quality processes and metrics to ensure high-quality data products are delivered to customers • Support the linking of clinical data to other data assets including molecular and imaging data assets, and specimen repositories • Support strategic decision making around data standards such as SDTM and AdAM • Serve as a single point of contact for all clinical-data related needs, questions and concerns about clinical data within data42 • Define the roadmap and planning of the clinical data pipeline team • In conjunction with a Scrum Master, guide an Agile team (5-10) who support technical data engineering tasks and human processes required to curate the data Minimum requirements What you’ll bring to the role • Master’s degree or higher in Computer Science, Data Engineering, Clinical Biostatistics, Statistical Programming Second degree in Data Science or statistics preferred (or any engineering field), or equivalent • Fluent in English (oral and written) • 10+ yrs working with clinical data • Operational experience running large data operations • Knowledge of and experience with CDISC standards including SDTM and AdAM • Knowledge of data pipeline and architectural decisions/trade-offs • Experience with semantics technologies and approaches (nice-to-have) • Have experience working in an environment that uses an Agile Sprint methodology • Integrity and transparency are core attributes Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous, and collaborative people like you are brought together in an inspiring environment, where you’re given opportunities to explore the power of digital and data. We are Novartis. Join us and help us reimagine medicine! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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13.07.2020

Novartis AG

External Innovative Partnership Head IHD (80-100%)

  • Novartis AG

  • 4051Basel

  • 13.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID298400BRPosition TitleExternal Innovative Partnership Head IHD (80-100%)Apply to Job Job Description 3000! That is the number of medical associates worldwide who will benefit from your work. As External Innovative Partnership Head, you will develop and lead global strategic partnerships for the Immunology, Hepatology & Dermatology (IHD) franchise in collaboration with cross-functional colleagues. Partnerships of strategic importance are intended to change or advance the clinical practice in disease areas relevant to the franchise, and are intended to improve patient outcomes and access to the right treatments at the right time. Relevant partnerships will include a wide variety of external stakeholders, such as professional societies, academic institutions, HTA bodies, other pharma companies and start-up companies Your responsibilities will include: • Build a strong network with key professional societies, patient organizations, insurers, payers, governments, health systems and start-up companies. • Identify key partnership opportunities for research or educational purposes. • Build a deep understanding of key health systems across the globe, and identify key needs and opportunities to improve clinical care and outcomes for patients with diseases included in the franchise. This may include (new ways of) evidence generation, education of clinical practioners, developing new relevant clinical endpoints, developing new clinical evaluation and/or management tools, etc. • Align within the franchise on key opportunities to improve clinical care and patient outcomes, and identify possible external partners/bodies who have aligned objectives and have an interest in collaboration. • Develop framework to support the identification, funding framework, evaluation of rigor and fit, engagement and development of strategic partnerships and technologies according to their fit to the business and priorities. Minimum requirements What you’ll bring to the role: • Advanced degree or equivalent education/degree in life science/healthcare required. MBA or equivalent preferred • 8-10+ years relevant pharma experience acquired at pharmaceutical companies, especially good understanding of the franchise disease area. • Ability to quickly establish credibility, influence and respect, set clear and ambitious goals, lead strategic analysis and innovation, and inspire collaboration from peers and stakeholders. • Strong organizational, interpersonal and influencing skills. Ability to probe, challenge and question appropriately and strive for continual improvement • Deep understanding healthcare ecosystem and Pharmaceutical industry interfaces • Strong understanding of drug development with proven ability to identify and deliver key evidence needs a diverse range of stakeholders. • Deep understanding of pharmaceutical value chain and its business processes, strong knowledge of clinical and real-world data Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionPHARMABusiness UnitGLOBAL MEDICAL AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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13.07.2020

Novartis AG

Analytical Expert/Analytical Project Leader (80-100% )

  • Novartis AG

  • 4040Basel

  • 13.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID296434BRPosition TitleAnalytical Expert/Analytical Project Leader (80-100%*)Apply to Job Job Description 50! The number of parenteral, topical, ophthalmic and inhaled projects of our compelling and rich development pipeline. We are searching for an Analytical Expert / Analytical Project Leader to support Analytical Research & Development (ARD). ARD sits within the Global Technical R&D department of Global Drug Development and plays an essential role in the characterization and analysis of Small Molecule Drug Substances and Drug Products from the time they leave the discovery laboratory until they are transferred to Commercial Production. We are looking for a highly motivated, experienced Analytical Expert / Analytical Project Leader with a strong background and experience in parenteral and late phase development to join our team. Expertise in oligonucleotide analytics is an asset. Responsibilities will include but are not limited to: • You will lead and manage analytical activities within a global project team (e. g. control strategy, specification setting strategy, method development, validation, stability and release testing. • Writing of analytical source documents (e.g Analytical methods, Specifications, Validation reports, Stability reports) • You are responsible to provide valuable input to the analytical CMC documents and support regulatory submissions • Prepare analytical project plans and be accountable to meet quality, timelines and budget for assigned projects. • Manage interactions and contribute to a high level of collaboration with internal and external stakeholders • Leading outsourced analytical activities at CROs / CDMOs and contribute to manage the external partnership. Minimum requirements What you’ll bring to the role: • PhD in analytical chemistry or equivalent and a minimum 5 years’ experience in the pharmaceutical industry in analytical development, preferable in late phase development for sterile parenteral products. Experience in Oligonucleotides analytic is a plus. • Proven knowledge in late phase parenteral development and filings • Proven leadership experience in managing development projects, ideally in a global matrix environment. • Excellent understanding and awareness of regulatory guidelines for analytical development. • Collaborative spirit, self-driven attitude, high level of learning agility are key attitudes • Strong quality focus and experience in a cGMP environment. • High level of motivation, excellent collaborative spirit and agility are key elements to our success Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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12.07.2020

Novartis AG

Senior Global Trial Manager (80-100% )

  • Novartis AG

  • 4051Basel

  • 12.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID296842BRPosition TitleSenior Global Trial Manager (80-100%*)Apply to Job Job Description 130,000! The average number of patients around the world that are actively participating in our clinical trials. As a member of our Trial Management team you will play an active role in ensuring patients have access to our clinical trials and make a difference in their lives. Your Responsibilities: • Contribute to all aspects of global clinical trial(s), under the oversight of the (Associate) Global Trial Director, to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). • Be a core member of the global cross-functional Clinical Trial Team (CTT); participate and report study progress and issues/resolution plan at the CTT meeting and write minutes; coordinate and chair trial sub teams within the scope of his/her delegated responsibilities. Extended member of the Global Clinical Team (GCT). • Implement issue resolution plans and act as point of contact for all site-related issues and procedural questions, and handle interactions with relevant line functions including data management, drug supply management, clinical development and Novartis Country Organizations • Development of study tools, guidelines and training materials as well as supporting the development of Case Report Forms (CRFs), and CRF completion guidelines. Ensure trial information/documents are reported within relevant trial repositories and tracking systems • Contribute to the development of clinical outsourcing specifications to facilitate bid process and selection of Contract Research Organizations (CROs); lead interface with CROs in collaboration with outsourcing management and line functions; ensure vendors meet quality standards; participate in the development/amendment of vendor contracts. Support the Global Trial Director with the development, management and tracking of the trial level life cycle budget. Minimum requirements What you'll bring to the role: • Advanced degree or equivalent education/degree in life science/healthcare, as well as 2-4 years of experience in clinical development (cross-functional, multicultural and international clinical trials; confirmed capabilities in supporting operational aspects of clinical trial related activities) • Knowledge of good Clinical Practice; comprehensive knowledge of clinical trial design; understanding of the overall drug development process • Shown ability to work either independently or in a team setting, to meet goals by leading compliance, budget and timelines • Validated networking skills and ability to share knowledge and experience amongst colleagues • Proficient English (oral and written) and excellent communication, organization and tracking skills **Please note that for this role we are only considering applications by candidates from Basel and surrounding, close-by areas. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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12.07.2020

Novartis AG

PostDoc in Immunology and Dermatology

  • Novartis AG

  • 4040Basel

  • 12.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID279987BRPosition TitlePostDoc in Immunology and DermatologyApply to Job Job Description 1 in 10 adults in Europe suffer from autoimmune or inflammatory diseases. The Department of Autoimmunity, Transplantation and Inflammation adresses this steadily growing burden on public Health with Research in the fields of rheumatology, dermatology and beyond. We are looking for a postdoctoral fellow to investigate the biology and downstream signaling of AD-associated cytokines including IL-17C on relevant skin target cells, in human ex vivo skin biopsies and in cytokine reporter/conditional knock-out mice. We provide state-of-the-art flow cytometry, proteomics and transcriptomics as well as biochemical and molecular technologies. In-house expertise in CRISPR, immunology and translational research as well as a variety of tools to interrogate cytokine expression, and pathway activation are available. The successful candidate should have experience in use of genetically modified mice and working with primary human skin and tissues to analyze cellular and biochemical regulation of cytokine signaling and should have knowledge of immunology. Knowledge in use of CRISPR and generation and evaluation of reporter and conditional knockout mice is highly desirable. #PhD Minimum requirements What you'll bring to the role: • PhD in molecular and cell biology and/or immunology (PhD students in the last year of their thesis work, are eligible to apply) Fluency in English, Knowledge of the German language will be advantageous • Knowledge of skin immunology, translational research and/or IL-17-receptor biology are a plus • Expertise in CRISPR and transgenic mouse research are highly regarded • Expertise in bioinformatics to interrogate complex datasets would be desirable • Strong publication record • Excellent analytical, communication and organizational skills Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionNIBRBusiness UnitAUTO/TRANS/INFL - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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12.07.2020

Novartis AG

Expert Regulatory Writer (80-100% )

  • Novartis AG

  • 4040Basel

  • 12.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID274930BRPosition TitleExpert Regulatory Writer (80-100%*)Apply to Job Job Description 200+ projects in development. 20 major approvals. 20 major submissions. And that’s just in 2018. This is your chance to help reimagine medicine in 2019 and beyond. Novartis is looking for dedicated individuals to join our Regulatory Writing team and contribute to developing our pipeline of drugs and biologics into innovative therapies for our patients worldwide. Read on for details about the role and how you can join a world-class organization at the forefront of the industry and how you can further your career. In this role, you will write, review and/or manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications. You will provide authoritative documentation-related consultancy to other line functions. You will coach/mentor and/or train less experienced writers. Your responsibilities will include (but are not limited to): ∙ Author, review and/or independently manage high quality clinical and safety documents for health authorities. ∙ Lead writing team for complex submissions, actively contributing to key messaging and pooling strategy, providing expert content guidance for) clinical submission documents, contributing to statistical analysis plans and presentation of outputs, and ensuring compliance of documentation to internal company standards and external regulatory guidelines. ∙ Program Writer for large and/or complex programs ensuring adequate medical writing resources are available for assigned program and consistency between documents. ∙ Lead process improvement in Regulatory Writing and Submissions and cross-functional initiatives and/or activities. ∙ Coach and/or mentor less experienced writers. Minimum requirements What you’ll bring to the role: ∙ ≥ 6 years medical writing experience or other relevant pharma industry experience combined with scientific and regulatory knowledge, plus expert knowledge of medical writing processes ∙ Expert knowledge of the global registering of drugs, and extensive experience and demonstrated record of accomplishment of leading complex submissions. ∙ Fluent English (oral and written) and excellent communication skills ∙ Proven ability to prioritize and manage multiple demands, projects and cross-functional teams. ∙ Future-oriented perspective and demonstrated ability to define and solve complex problems. WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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12.07.2020

Novartis AG

Head Patient Safety, Ophthalmology (80-100% )

  • Novartis AG

  • 4051Basel

  • 12.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID296898BRPosition TitleHead Patient Safety, Ophthalmology (80-100%*)Apply to Job Job Description 80% of all vision impairment can be prevented or cured. Novartis Ophthalmology is the global leader in this area with recognized products in Retina, Glaucoma, Infections/Inflammation and Allergy. As Head Patient Safety (HPS) Ophthalmology you will successfully lead the Ophthalmology Therapeutic area/Development unit (TA/DU) of the Medical Safety organization to improve patients’ lives and impact on overall Novartis results through robust safety evaluation expertise and medical innovation. You will ensure optimal patient safety as first priority by developing a state of the art safety strategy, driving medical safety processes and capabilities and having accountability for safety compliance within the TA/DU. You have a key responsibility in building an efficient team within the TA/DU and attracting, retaining and developing talents. Your main responsibilities include, but are not limited to: • Leading efficiently and successfully a team of physicians and scientists, accountable for medical and science-driven contribution to Benefit-Risk evaluation of Novartis products in the field of Ophthalmology • Enhancing scientific and clinical experience of the team through continuous training and coaching. Building the talent pipeline, attracting, retaining and developing talents within Medical Safety and TA/DU. • High quality, timely and standardized Medical Safety deliverables across the TA/DU. Ensuring that potential safety issues affecting the Benefit-Risk profile of the product are identified promptly and communicated/escalated appropriately • Leading/ coordinating the preparation of medical stewardship data/information for Novartis boards, crisis management teams, and Health Authorities for TA/DU safety issues • Managing productive cross-functional Medical Safety collaborations within CMO&PS and across line functions, e.g. Clinical Development, Medical Affairs, Regulatory Affairs • Adequate and proper management of resources to support all projects and maintain business continuity within the TA/DU. Minimum requirements What you will bring to the role: • Medical degree required. Specialty Board Certification desirable. Useful additional degrees: Post-graduate degree in Pharmaceutical Medicine; Master of Public Health in Epidemiology (or equivalent) • At least 10 years in drug development in a major pharmaceutical company, including 7 years in global medical safety, preferably in the ophthalmology area • Experience in responsible/leading roles in clinical or safety through complete submission process and in presenting data to major Health Authorities • Strong leadership skills including coaching, motivating, directing, and fostering teamwork; Experience in leading cross-functional, multi-cultural teams • Ability to develop and maintain effective working relationships with subordinates, superiors and peers; Strong negotiation and conflict management skills *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitCMO & PATIENT SAFETY GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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12.07.2020

Novartis AG

Global Marketing Director, Cardio-Renal-Metabolic

  • Novartis AG

  • 4051Basel

  • 12.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID288573BRPosition TitleGlobal Marketing Director, Cardio-Renal-MetabolicApply to Job Job Description 50 Million! That is the number of how many secondary prevention patients worldwide do not achieve LDL-C lowering goals and remain at increased cardiovascular risk despite being on current standard of care. As part of Novartis you are committed to reimagining medicines for patients with dyslipidemia and to helping realizing your potential and being part of a remarkable employee community. You will work with hardworking individuals - experts in their field and be inspired by some of the best leaders in the industry. This is a role waiting for you to put your own stamp on it. Your responsibilities will include: • Develop the launch strategy with the global crossfunctional teams, regions and key countries • Develop the vision, the aspiration and the positioning of the brand • Lead the development of the brand messaging and communication • In partnership with medical, build a robust scientific platform and engage with key experts in the field • In partnership with patient access, develop pricing options and innovative access models • Provides commercial input to product development, including new indications and life cycle management • Design and implement differentiate launch tactics • Collaborate with countries to ensure wide implementation [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you will bring to the role: • University degree in Science and/or degree in Business Marketing, master preferred • At least 10 years of sales and marketing experience, ideally a mix of both in-market and global experience • Launch experience – cardio and multi-country preferred • A passion for trying new approaches Desirable requirements: • An experience in the vaccines business would be a plus WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

11.07.2020

Novartis AG

Expert Global Trial Manager (80-100% )

  • Novartis AG

  • 4040Basel

  • 11.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID296839BRPosition TitleExpert Global Trial Manager (80-100%*)Apply to Job Job Description 130,000! The average number of patients around the world that are actively participating in our clinical trials. As a member of our Trial Management team you will play an active role in ensuring patients have access to our clinical trials and make a difference in their lives. Your Responsibilities: • Contribute to all aspects of global clinical trial(s), under the oversight of the (Associate) Global Trial Director, to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead certain parts of global clinical trial(s). • Be a core member of the global cross-functional Clinical Trial Team (CTT); participate and report study progress and issues/resolution plan at the CTT meeting and write minutes; coordinate and chair trial sub teams within the scope of his/her delegated responsibilities. Extended member of the Global Clinical Team (GCT). • Contribute to the creation and execution of an operational risk management plan, highlighting potential risks and actions; Implement issue resolution plans and act as point of contact for all site-related issues and procedural questions, and lead interactions with relevant line functions including data management, drug supply management, clinical development and Novartis Country Organizations • Development of study tools, guidelines and training materials as well as supporting the development of Case Report Forms (CRFs), and CRF completion guidelines. Ensure trial information/documents are reported within relevant trial repositories and tracking systems • Contribute to the development of clinical outsourcing specifications to facilitate bid process and selection of Contract Research Organizations (CROs); lead interface with CROs in collaboration with outsourcing management and line functions; ensure vendors meet quality standards; contribute to the development/amendment of vendor contracts. Support the Global Trial Director with the development, management and tracking of the trial level life cycle budget. Minimum requirements What you'll bring to the role: • Advanced degree or equivalent education/degree in life science/healthcare, as well as 3-5 years of experience in clinical development with a minimum of 2 years in global clinical research (cross-functional, multicultural and international clinical trials; shown capabilities in supporting operational aspects of clinical trial related activities) • Knowledge of good Clinical Practice; comprehensive knowledge of clinical trial design; understanding of the overall drug development process • Validated ability to work either independently or in a team setting, with strong operational skills and demonstrated ability to meet goals by leading compliance, budget and timelines • Networking skills and ability to share knowledge and experience amongst colleagues • Proficient English (oral and written) and excellent communication, organization and tracking skills **Please note that for this role we are only considering applications by candidates from Basel and surrounding, close-by areas. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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10.07.2020

Novartis AG

Group Head Qualification and Logistics (80-100%)

  • Novartis AG

  • 4051Basel

  • 10.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID297951BRPosition TitleGroup Head Qualification and Logistics (80-100%)*Apply to Job Job Description 50+! That’s the number of promising projects in development that you will support by ensuring compliance and high quality within Biologics Analytical Operations. This role is waiting for you to enable the release of our medicines and ultimately to help improving and extending people’s life. In this role, you will lead the Compliance and Logistics team (qualification of equipment and CSV, GMP officer, Training coordinator, Sample Management) to ensure compliance of laboratory related activities and associated Quality systems with the requirements of the Novartis Quality Manual and all relevant regulatory and legislative requirements across the lifecycle of the products. Your responsibilities: • Provide strategic leadership and actively contribute to budget and resource forecast • Supervise timely execution of all activities in collaboration with the team facilitator - Provide scientific and technical expertise - Identify and resolve conflict situations with empathy - Inspire, coach and lead team members (including supporting people development plan) • Ensure compliance to cGMP and HSE according to applicable regulatory requirements and guidelines. Support Health Authority inspections and Audits. • Actively participate/lead in cross-cultural networks and global initiatives • Pro-actively seek opportunities for productivity improvements and coordinate their implementation Minimum requirements What you’ll bring to the role: • Advanced degree in Sciences/healthcare is required. PhD is preferable. • Fluent in English (oral and written). German is highly desirable. • At least 10 years relevant experience with excellent knowledge of GxP standards and compliance processes, or equivalent experience • Excellent leadership skills including experience in managing budget and resources, as well as Objective Setting and Performance Management • Good knowledge of software and computer tools • You are an effective communicator and bring demonstrated experience in risk management and change management • Competencies in Operational Excellence and Stakeholder Engagement Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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10.07.2020

Novartis AG

Senior Drug Substance Project Leader (80-100 )

  • Novartis AG

  • 4051Basel

  • 10.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID293265BRPosition TitleSenior Drug Substance Project Leader (80-100*)Apply to Job Job Description More than 500! The number of clinical trials ongoing worldwide for CAR-T cell therapies. We are looking for a senior Drug Substance Project Leader in TD-NBE, to develop and drive technologies in the field of Cell and Gene Therapies. The candidate will be accountable for general and strategic Downstream process (DSP) aspects in this area with specify focus on Lentiviral Vectors. The role comprises the scientific leadership as the DSP process specialist in the project team as well as facilitation and tracking of major process development and manufacturing activities to ensure timely and consistent process development for Cell and Gene Therapy projects. Within the CGT field, the candidate will build and establish expertise in Lentiviral Vector process development and manufacturing with focus on downstream technologies. Your Responsibilities: • DSP process and technology strategy for Cell and Gene Therapy projects in early phase development, with focus on Lentiviral Vector based Cell and Gene Therapies • Single point of contact for Technical Project Leaders and other partners for key DSP process aspects • Planning and tracking of major DS process development and manufacturing activities and deliverables in collaboration with the Line Function • Represent the DS subteam as core member in the technical CMC project team • Coordinate and provide input to Reg-CMC on DS processes (e.g. in response to questions from regulatory authorities, Briefing Books, preparation of Health Authority meetings). Minimum requirements What you’ll bring to the role: • M.Sc. or Ph.D. in Biotechnology, Bioengineering or equivalent with 5-8 years experience in downstream processing of Lentiviral Vectors and/or viruses in an industrial environment • Advanced knowledge in purification technologies in the field of Cell and Gene Therapy and experience in Biosafety regulations, BL-1 and BL-2 • Validated management skills with respect to planning/tracking, prioritization and project timelines • Experience with CMO management and collaboration with external partners • Sound written and oral communication skills and concise data presentation in English required Desirable Requirements: • Familiarity with GMP requirements • Experience with downstream processes for diverse Biologics formats is an advantage Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

09.07.2020

Novartis AG

Director/Associate Director, Real World Evidence and Data Science

  • Novartis AG

  • 4051Basel

  • 09.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID286314BRPosition TitleDirector/Associate Director, Real World Evidence and Data ScienceApply to Job Job Description 21st Century evolution and innovation in digital technologies, data and advanced analytics is rapidly changing the healthcare environment. We believe that Real World Evidence will transform healthcare decision-making as part of that revolution. As a Real World Evidence (RWE) Scientist within the RWE Center of Excellence (CoE), you will be responsible for developing RWE strategies that deliver innovative and scientifically robust evidence. You will collaborate with multiple stakeholders and partner throughout the organization to design RWE studies and implement analyses to address product- and disease-area research questions, which will inform business decisions about the research and development of our products as well as support healthcare decisions by patients, physicians, health authorities, payers, and policy-makers. This will require a deep understanding of observational research methods to define appropriate research questions and data sources, study design, rigorous and fit-for-purpose analytical approaches as well as strong communication skills to summarize and present findings. You will need excellent technical, strategic, leadership, collaboration and communication skills, as well as an entrepreneurial mindset, to work with and through others, to reimagine the way we use data and analytics to develop and deliver medicines for patients. As a RWE Scientist, you will drive the development of RWE approaches, techniques, and standards using your expertise in an assigned area in the Oncology Business Unit. You will work closely with franchises in regions and key countries to enable RWE and sharing of best practices across geographies. Your responsibilities will include: • Develop and drive RWE strategies, in collaboration with internal partners, to ensure that the value of our medicines is fully supported by evidence both globally and locally • Lead cross-functional Real World Evidence team consisting of internal partners with the clear objective to deliver scientifically valid and robust evidence to support all stages of product development, and to drive global and local value demonstration • Ask the right scientific questions, understand the evidence needs for product development, regulatory and market access, and ideate and make recommendations on fit-for-purpose data and analytics solutions • Work closely with regions and countries to develop timely, meaningful and robust evidence to support product value demonstration aligned with local needs (patient access, reimbursement, medical education, and patient advocacy) • Foster learning with internal and external partners by using analytical tools and applications to broaden data accessibility and advance our proficiency/efficiency in understanding and using the data appropriately • Stay current with and adopt emergent analytical methodologies, tools and applications to ensure fit-for-purpose and innovative approaches • Apply rigor in study design and analytical methods; design a fit-for-purpose analysis plan, assess effective ways of presenting and delivering the results to maximize impact and interpretability; implement and/or oversee the study, including its reporting; ensure compliance with applicable pharma industry regulations and standards • Communicate findings to internal stakeholders, regulatory, health technology assessment (HTA) bodies and scientific communities; publish results; participate in external meetings and forums to present your insights (e.g. congress/conference) • Collaborate and contribute to functional, cross-functional, enterprise-wide or external RWE communities, networks, collaborations, initiatives or goals on knowledge-sharing, methodologies, innovations, technology, IT infrastructure, policy-shaping, processes, etc. to enable broader and more effective use of data and analytics to reimagine cancer treatment • Provide expert input to evaluate external technologies or capabilities in data and analytics according to their strategic fit to the business and priorities Minimum requirements What you’ll bring to the role: • Advanced degree or equivalent education/degree in life science/ healthcare required. PhD or equivalent preferred • Fluent English (oral and written) • 5+ years relevant experience acquired at pharmaceutical companies, academia, healthcare provider/ Payer/ HTA, or relevant consultancy companies • Deep understanding and experience of Real World Data/ Real World Evidence or related disciplines to generate scientifically rigorous and value evidence from secondary data sources • Strong understanding of drug development with proven ability to identify and deliver key evidence needs for Clinical Development, Commercial, Market Access, HEOR, Medical, Safety, Regulatory stakeholders • Demonstrated track record of leading and executing research projects using real world data from claims, electronic health records, registries, biobanks, or digital applications, including publications • Excellent knowledge of observational and/ or epidemiological research methodology and statistical methods • Demonstrated experience with managing project scope and driving delivery in a fast evolving environment We are seeking candidates at both the Principal and Senior Real World Evidence Scientist levels. The level of skills and experience you bring to the role will determine which level you are considered for. WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarket AccessJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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07.07.2020

Novartis AG

Intern Global Brand Team - Ophthalmology

  • Novartis AG

  • 4040Basel

  • 07.07.2020

  • Praktikumsstelle

Back to Previous Page Job ID298533BRPosition TitleIntern Global Brand Team – OphthalmologyApply to Job Job Description Over 70 the product available in our ophthalmology portfolio in high unmet need conditions - we develop and deliver life-changing medicines and therapies for diseases and conditions from front to back of the eye, enabled by data and transformative technologies We are looking for an intern who will support the Global team of a launch brand in executing the Global Brand strategy. Your responsibilities include, but are not limited to: • Support the team in their internal communication (monthly newsletter, brand site updates, Yammer, announcements, etc.) • Organization of Brand team meetings governance e.g. calendar, agenda organization and writing of minutes / follow up • Support global congresses presence • Liaise with agencies for ad-hoc deliverables • Support in creation of Power Point presentation and ad hoc documents • Management of other ad hoc projects Minimum requirements What you’ll bring to the role: • Master degree in Life Sciences (Biology / Biotechnology), Pharmacy, Economics or Marketing (graduation not longer than 2 years ago) • Fluent in English (written and spoken), additional language is a plus • Knowledge of Pharma environment, previous experience in Pharma, life science or consulting preferable • “Can do” attitude, proactivity, ability to efficiently work in a team, collaborative mindset • Previous experience in a multinational company preferable • Very good knowledge in MS Office • Good communication skills Timing: September 2020 Duration: 6-12 months 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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07.07.2020

Novartis AG

Internship FRA Ops Master Data

  • Novartis AG

  • 4040Basel

  • 07.07.2020

  • Praktikumsstelle

Back to Previous Page Job ID298527BRPosition TitleInternship FRA Ops Master DataApply to Job Job Description 700! The number of days we can get therapies faster to patients applying Technology innovation. Your reponsibilities: The Internship will support the Global Finance Master Data group in running processes linked to Finance master data used in Novartis. She/he will ensures that data validation, data entry, data quality, reporting and analysis are in place and managed in accordance with defined data standards and operating procedures. Great opportunity to demonstrate innovation in a very visible area in Finance and to advance and learn alongside accomplished business leaders Your responsibilities includes, but are not limited to: • Execute processes linked to applications managed by the Global Finance Master data team (GFMD) • Support operations and ad-hoc requests for GFMD process / system. • Maintain process documentation for master data objects and share processes and technical knowledge and best practices openly to other team members, locally and globally • Work with other departments in order to create and utilize accurate reporting • Support the Global Finance Master Data Group in their communication and document management (Sharepoint, Intranet Minimum requirements What you'll bring to the role: Currently enrolled in MSc or just finished university degree in Business Administration / Economics / Finance or Chartered Accountant / Technology-related Engineering • Fluent in English (written and spoken), additional language is a plus • Team player • Very good knowledge in MS Excel required • Good communication skills • Analytical mind in combination with a high degree of personal responsibility, conscientiousness and proactivity Why consider Novartis ? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionNBSBusiness UnitFRA OPERATIONS NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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07.07.2020

Novartis AG

Human Factors/Usability Engineer (80 - 100%)

  • Novartis AG

  • 4040Basel

  • 07.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID297749BRPosition TitleHuman Factors/Usability Engineer (80 – 100%)*Apply to Job Job Description 3! This is the maximum number of steps that a user accepts to do when using an injection device! Designing simple devices is key to our success! To support the medical device development team we are seeking a Human Factors/Usability Engineer to lead human factors activities in developing medical devices/combination products and apps, from early concept phase through to late phase development. You will be part of multidisciplinary and international teams, spanning across multiple projects, with human factors engineering being a key element for success. Your strong communication and negotiation skills will be key to influence multiple partners. You will also act as a key advocate for human factors principles across the company. You will provide expert input to device development projects to establish system, design, and operating requirements as well as influencing the design of packaging, labeling and the user interface. This position may require up to 15% travel. Your Responsibilities: • Managing the Human Factors/Usability activities during the design development. This includes: user needs identification, development of user profiles and use scenarios, task analysis, use-related risk analysis, generation of hardware and software design concepts, preparing story boards, developing wire frame for apps, training requirements, user interface specification, • Independently manage the user studies (formative and summative) to evaluate the user interface and present recommendations to optimize the design. • Develop the Human Factors/Usability strategy for projects: plan human factors activities according to project requirements, manage external partners supporting the device development and evaluation. • Provide Human Factors/Usability expertise in a broader cross-functional development team • Develop and design instructions for use, design story boards, wireframe • Support definition of internal procedures and templates for the execution of Human Factors/Usability engineering activities in compliance with both company quality assurance standards and applicable regulations. Minimum requirements What you’ll bring to the role: • Bachelor’s or Master degree in engineering, ergonomics, psychology, human factors, usability, user interface design, industrial design/graphic design or related field. • Excellent skills in English, verbal and written are required. Other language skills, e.g. French, German are advantageous. • Several years of experience in applying Human Factors Engineering/Usability to medical devices development, preferably in the pharmaceutical industry - therefore you have an excellent understanding of applying Human Factors/UsabilityEngineering processes to medical device development from concept generation to health authority submission. • Experience in developing apps, software and/or graphic design (InDesign, Adobe suite, Axure, Photoshop etc) • Experience in project / program management • Experience in managing user studies (performed by vendors or self-managed) • Good understanding of the risk management activities Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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07.07.2020

Novartis AG

Trial Operations Manager (80-100% )

  • Novartis AG

  • 4051Basel

  • 07.07.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID297765BRPosition TitleTrial Operations Manager (80-100%*)Apply to Job Job Description 46’000! That is the number of patients in clinical trials at Novartis. Within the Trial Monitoring organization we drive execution of clinical trials in countries ensuring highest quality monitoring at sites. Under the direction of the Unit Head, you will be accountable for the oversight and coordination of the global monitoring operational aspects of assigned clinical trials, from start-up to close-out, in collaboration with the Clinical Trial Team, in compliance with Novartis processes, GCP, ICH and regulatory requirements. The scope of your activities range from trial start-up to close-out including strategic and operational planning, feasibility assessment, trial allocation, start-up activities coordination, patient recruitment, clinical data collection and delivery of timely, high quality submission data, sites close-out, audit organization and inspection preparation activities. You will contribute to the implementation of the Trial Monitoring strategy in the assigned clinical trials. Your responsibilities: • Partner and agree with GPT/GCT/ICT/CTT on trials execution plans and timeline commitments in alignment with Trial Monitoring strategy and on behalf of the Trial Monitoring organization to achieve global and regional/local business. Communicate planned milestones to Trial Monitoring partners and update your partners on operational activities at the Region/CPO level, during the course of the trials to meet GPT Objectives • Participate in the development of innovative solutions in clinical trial planning and execution, including country, site and patient engagement to ensure the delivery of assigned studies on time • Consistently read/review the content of all monitoring visit reports for the assigned trial to identify trends and issues. Appropriately raise issues in a timely manner and ensure resolution. Communicate with field monitors on a regular basis to assure accurate adherence to protocol, timelines and other trial related topics. • You are responsible for trials execution according to enrolment commitment and timelines delivered. You will develop planning for prospective management of clinical trials including operational risks for each phase of the trial (Start-up, Data collection and cleaning) using available internal and external resources (competitive landscape regional strategies, data, statistical plan) • Evaluate potential challenges or risks within the protocol and operational aspects of the study; assessing impacts, developing risk management plans and communicating/escalating, as appropriate • Review, approve, and ensure updates to CCGs as appropriate during trial conduct. Perform User Acceptance Testing for EDC system. Contribute to the development of the DHP and DRP. Distribute regulatory documents such as Protocol, ICFs, IBs and all related Amendments to CPOs • Author the monitoring plan and following updates, trains monitors and facilitate the development of trial level operational training materials. Drive trial startup by coordinating preparation of FPP by respective CTT LF members, acceptance by CPOs, and tracking progress of SSU milestones (RIS, SIVs, FPFVs) • Be accountable for recruitment activities as per targets and reviews enrolment at the trial level, including responsibility for approval of changing recruitment dedication. Be responsible for forecasting, setting up contingency planning to ensure recruitment targets are achieved in accordance with trial execution plan, including communication of timelines for major deliverables from start to end of enrollment, in coordination with CTT, regions and CPOs (with Clinical Study Managers) • Coordinate clinical data collection as per plan, including contingency planning and communication of timelines for major database lock deliverables, in coordination with the Data Review Team, regions, and CPOs and ensure timely site close-out activities Minimum requirements What you will bring to the role: • Advanced degree in science (e.g. pharmacy, biomedical sciences or related field) as well as fluency in English, with excellent communication and negotiation skills • Experience in clinical research, in planning, executing and/or monitoring clinical trials (preferably in Clinical Operations Management) • Solid understanding of all aspects of clinical drug development with particular emphasis on clinical trial design, trial execution, project management and operations as well as international standards (GCP/ICH) • Demonstrated ability to collaborate across partner functions in a complex matrix environment • Excellent project management skills with ability to problem solve and mediate complex issues Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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06.07.2020

Novartis AG

Senior Order Manager / Scheduler

  • Novartis AG

  • 4051Basel

  • 06.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID298393BRPosition TitleSenior Order Manager / SchedulerApply to Job Job Description 10 days! That is how long we treat a patient’s T-cells, before we return them to potentially save this patient’s live. To support such novel, personalized treatment by ensuring application of correct artwork, is a unique challenge within Novartis with immediate patient impact. Your responsibilities include, but not limited to: • Monitor and maintain correct system transactions related to order management processes according to defined business cases (e.g. intragroup supplies) based on planning & master data parameters including the up-to-date status of the order at any point in time • Prepare and ensure availability of all relevant documentations and approvals needed to guarantee steadily product flow • Provide guidance and assist assigned customers for returns, write-off’s, rebates and credit/debit notes according to the established SOPs and guidelines. • Perform system bookings for returns and issue credit notes in a timely manner taking into consideration month-end, quarter-end and year-end financial timelines. • Maintain a proactive and close communication with customers and suppliers aligning daily business to guarantee a high customer service level at all times • Facilitate communication of intercompany customers and suppliers in alignment with direct communication principles and actively support in case no direct communication is in place What you’ll bring to the role: • Higher education (Bachelor degree) in Supply Chain Management, Business Administration or Industrial Engineering, at least vocational education in commercial professions complemented by additional training in business administration resp. supply chain management • English and German – fluent written and spoken • At least 5-7 years of experience in Supply Chain role in Health Care, Consumer Goods, Chemical or another process industry • Comprehensive understanding of Supply Chain processes incl. customer service and vendor management • At least 3 years of experience in SAP usage (advanced user knowledge), good understanding of ERP implementation methodology and Computer literacy: Office applications (Excel, Power Point, Word) and Visio • Must be a confident personality with a can do attitude who is willing to expose issues and work collaboratively across functions to put in place systemic solutions that address root cause and deliver on expected timelines Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We are Novartis. Join us and help us reimagine medicine. Minimum requirements What you’ll bring to the role: • Higher education (Bachelor degree) in Supply Chain Management, Business Administration or Industrial Engineering, at least vocational education in commercial professions complemented by additional training in business administration resp. supply chain management • English and German – fluent written and spoken • At least 5-7 years of experience in Supply Chain role in Health Care, Consumer Goods, Chemical or another process industry • Comprehensive understanding of Supply Chain processes incl. customer service and vendor management • At least 3 years of experience in SAP usage (advanced user knowledge), good understanding of ERP implementation methodology and Computer literacy: Office applications (Excel, Power Point, Word) and Visio • Must be a confident personality with a can do attitude who is willing to expose issues and work collaboratively across functions to put in place systemic solutions that address root cause and deliver on expected timelinesDivisionNovartis Technical OperationsBusiness UnitNTO SUPPLY CHAINLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaTechnical OperationsJob TypeFull TimeEmployment TypeTemporaryShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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06.07.2020

Novartis AG

Post-Doc/ Early Talent Program

  • Novartis AG

  • 4040Basel

  • 06.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID298488BRPosition TitlePost-Doc/ Early Talent ProgramApply to Job Job Description Biocatalysis Chemist in Chemical and Analytical Development (Early Talent Program) 24! That’s the number of months that you will be spending in Chemical and Analytical Development (CHAD) department enrolled in our highly dynamic Early Talent Program. We are looking for highly motivated recent Postgraduates (i.e. PhD) to support and expand the use of biocatalysis technology in our department. This program is a unique opportunity to collect first experience of applied biocatalysis sciences in the Pharmaceutical industry. Several rotations within various labs in CHAD Basel (e.g. synthetic labs supporting route and process development), manufacturing pilot plant, as well as being part of a protein engineering team to develop effective enzyme, will provide a comprehensive overview on drug development within Novartis. During these rotations, you will be exposed to current standards in safety, quality and training systems and good manufacturing practice (GMP). It will not only enable you to transfer your theoretical know-how into practice, but also to grow your internal network for your future career in the Pharmaceutical industry. Your responsibilities: Your responsibilities include, but are not limited to: • Investigate the feasibility of applying a variety of scientific principles and concepts to potential innovations, processes or products; plans and executes lab experiments • Develop Biocatalytic processes on relevant project within Novartis portfolio including characterization of critical parameters • Be part of a protein engineering team for several months periods to develop effective enzyme used in process R&D • Support standard synthetic and analytical development activities on portfolio relevant projects • Support scale-up activities, transfer to pilot plants Minimum requirements What you’ll bring to the role: • Preferentially, a completed PhD in Organic Chemistry with a strong focus on Biocatalysis or related discipline (e.g Chemical Engineering). • Fluency in English, additional German proficiency is a plus. • Biochemical and/or Bioengineering knowledge as well as strong knowledge in organic chemistry is required • An excellent track record of original research and extensive experience in developing biocatalyzed transformations using “state of the art” technologies. • Proficient in utilization of special tools/equipment, lab automation tools. • Good knowledge of software and computer tools (e.g. MS Office). • Ready to expand own knowledge, open minded with an international outlook. • Finally, since all work takes place in multidisciplinary project teams, track record on strong interpersonal and communication skills are required. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine. Duration of employment and start date 24 months from January 2021. Deadline for application: September 30th, 2020.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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29.07.2020

Novartis AG

QC Scientist Bioanalytics CGT

  • Novartis AG

  • 9063Stein (Säckingen)

  • 29.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID299810BRPosition TitleQC Scientist Bioanalytics CGTApply to Job Job Description 10 days! That is how long we treat a patient’s T-cells, before we return them to potentially save this patient’s live. To support such novel, personalized treatment by defining and implementing the microbial control strategy, is a unique challenge within Novartis with immediate patient impact. Your responsibilities: Your responsibilities include, but are not limited to: • Plan and perform Bio-Analytical testing such as Flow Cytometry, ELISA, cell count, cell viability, residual bead assessment, qPCR, Potency, in collaboration with experi-enced team members, if necessary • Perform all testing and activities compliantly following appropriate SOPs and procedures • Maintain controls, reagents and reference standards to support testing • Work on shifts covering daytime / evening and one or both weekend days • Review/approve data generated by other team members • Train others • Contributes to the setup and optimization of infrastructure or specialized facilities e.g. cell culture or qPCR labs as an expert w/ adequate guidance • Evaluate/qualify and maintain lab equipment • Execute validation/transfers/optimization of test methods as per appropriate protocols • Contribute to OOS/OOE and deviation investigations • Participate in deviation investigation/CAPA implementation in a timely manner • Support 5S and Lean projects • Continually identify areas for improvements in project work • Interface with regulatory agencies during audits • Support tracking and trending systems, and programs which assist in the testing, evaluation and monitoring of quality and efficiency • Review Bioanalytics documents to ensure completeness, accuracy, consistency and clarity • Generate/revise protocols/reports, SOPs, forms, laboratory data sheets (LDS) • Generate Cell Banks • Review of laboratory logbooks and laboratory cleaning Minimum requirements What you’ll bring to the role: • BA or MS in biology, chemistry, biochemistry, microbiology or other related science • Fluent in English and local language • 3-8 years of experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device • Industry Knowledge of cGMP and GLP • Knowledge of LabWare LIMS and/or other QC data systems • Thorough knowledge of bioassay test methods, as appropriate • Ability to communicate clearly with a variety of individuals in various aspects of Novartis operations • Detail-oriented with expertise in problem solving and solid decision making abilities • Strong written and verbal communication skills are essential Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNovartis Technical OperationsBusiness UnitNTO QUALITYLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeTemporaryShift WorkYes Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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29.07.2020

Novartis AG

QA Specialist CGT

  • Novartis AG

  • 4332Stein (Säckingen)

  • 29.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID299813BRPosition TitleQA Specialist CGTApply to Job Job Description 10 days! That is how long we treat a patient’s T-cells, before we return them to potentially save this patient’s live. To support such novel, personalized treatment is a unique challenge within Novartis with immediate patient impact. The QA Specialist CGT is a member of the QA Operations Release Team that is responsible for the final release of product and overall quality oversight of the production and other operational units within Stein C> manufacturing. The team ensures that the quality strategy is implemented and that there is a continuous drive to improve product and process quality within the operational units. Your responsibilities: Your responsibilities include, but are not limited to: Support in establishing the SOP landscape relevant for QA Operations, GMP compliant BRR, Apheresis receipt and lot disposition processes during project phase. Independent, flexible processing of all activities related to the release of product during clinical and commercial manufacturing: Technical release of primary packed and finished product, media and apheresis, evaluation and decision of deviations including robust CAPA management, review/approval of batch related quality relevant documents ( e.g. validation documents, transfer documents, APR/PQR), review/ approval of MBRs, review/ approval of executed batch records, audit and inspection support. Minimum requirements What you’ll bring to the role: • Bachelor of Science or Master of Science in Biology, Chemistry, Biochemistry, Microbiology or other related science. • Good understanding of cGMP • Fluent English, German skills desired • 0-5 years of experiences in pharmaceutical QA, QC or production environment; IT-Knowledge (MS Office, SAP, Trackwise, MES) • Ability to communicate clearly with a variety of individuals across different departments in a matrix organization Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNovartis Technical OperationsBusiness UnitNTO QUALITYLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeTemporaryShift WorkYes Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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29.07.2020

Novartis AG

QA Specialist, Cell & Gene Therapies (CGT)

  • Novartis AG

  • 9655Stein (Säckingen)

  • 29.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID299830BRPosition TitleQA Specialist, Cell & Gene Therapies (CGT)Apply to Job Job Description 10 days! That is how long we treat a patient’s T-cells, before we return them in order to potentially save this patient’s live. To support such novel, personalized treatment by ensuring application of correct artwork, is a unique challenge within Novartis with immediate patient impact. The QA Specialist is a member of the QA Analytics & Aseptics Team in QA Operations that is responsible for the final overall quality oversight of the production, Quality Control and other operational units within Stein C & GT manufacturing. The QA Operations team ensures that the quality strategy is implemented and that there is a continuous drive to improve product and process quality within the operational units. Your responsibilities: Your responsibilities include, but are not limited to: • QA Oversight of CGT Quality Control (QC) Unit. This includes QA for release analytics of media and finished product, e.g. FACS, qPCR, ELISA, beads and virus analytics. • QA Oversight of CGT Manufacturing Unit/shopfloor with regard to aseptic topics, e.g. hygiene, aseptic working technique, environmental monitoring, best practice in clean rooms. • Writing, review and/or approval of validation and qualification documents (plans and reports), Out of Specification records, Deviations and other Quality Events, Change Requests, SOPs, risk assessments, testing monographs, transfer documents, lab protocols, trending reports, annual reports, stability reports, certificate of analysis (CoA). • Be point of contact regarding QA questions in quality control and aseptic questions in manufacturing unit, provide ad hoc decisions and act as trainer and advisor on aforementioned topics. • Participate and key person in health authority and internal inspections. Minimum requirements What you’ll bring to the role: • 2-5 years of GMP/GxP experience in pharmaceutical QC, QA, MS&T or production environment, preferably in sterile manufacturing or Cell & Gene (ATMPs) • Strong knowledge and expertise in Quality Control and Aseptics • Strong written and verbal communication skills, ability to communicate clearly with a variety of individuals in various aspects of Novartis operations (QA, QC, PU, MS&T, Logistics) • IT-Knowledge (MS Office, SAP, Outlook, Trackwise, LIMS) Desirable requirements: • BA or MS in Cell/Molecular Biology, Genetics, Biochemistry, Microbiology or related discipline • Fluent in German, good working knowledge in English Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.We are Novartis. Join us and help us reimagine medicine.DivisionNovartis Technical OperationsBusiness UnitNTO QUALITYLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeTemporaryShift WorkYes Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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27.07.2020

Novartis AG

QA Specialist CGT

  • Novartis AG

  • 9655Stein (Säckingen)

  • 27.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID273386BRPosition TitleQA Specialist CGTApply to Job Job Description 10 days! That is how long we treat a patient’s T-cells, before we return them to potentially save this patient’s live. To support such novel, personalized treatment is a unique challenge within Novartis with immediate patient impact. The QA Specialist CGT is a member of the QA Operations Release Team that is responsible for the final release of product and overall quality oversight of the production and other operational units within Stein C&GT manufacturing. The team ensures that the quality strategy is implemented and that there is a continuous drive to improve product and process quality within the operational units. Your responsibilities: Your responsibilities include, but are not limited to: Support in establishing the SOP landscape relevant for QA Operations, GMP compliant BRR, Apheresis receipt and lot disposition processes during project phase. Independent, flexible processing of all activities related to the release of product during clinical and commercial manufacturing: Technical release of primary packed and finished product, media and apheresis, evaluation and decision of deviations including robust CAPA management, review/approval of batch related quality relevant documents ( e.g. validation documents, transfer documents, APR/PQR), review/ approval of MBRs, review/ approval of executed batch records, audit and inspection support. Minimum requirements What you’ll bring to the role: • Bachelor of Science or Master of Science in Biology, Chemistry, Biochemistry, Microbiology or other related science. • Good understanding of cGMP • Fluent English, German skills desired • 0-5 years of experiences in pharmaceutical QA, QC or production environment; IT-Knowledge (MS Office, SAP, Trackwise, MES) • Ability to communicate clearly with a variety of individuals across different departments in a matrix organizationDivisionNovartis Technical OperationsBusiness UnitNTO QUALITYLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeRegularShift WorkYes Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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25.07.2020

Novartis AG

QA Specialist, Cell & Gene Therapies (CGT)

  • Novartis AG

  • 9063Stein (Säckingen)

  • 25.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID273400BRPosition TitleQA Specialist, Cell & Gene Therapies (CGT)Apply to Job Job Description 10 days! That is how long we treat a patient’s T-cells, before we return them in order to potentially save this patient’s live. To support such novel, personalized treatment by ensuring application of correct artwork, is a unique challenge within Novartis with immediate patient impact. The QA Specialist is a member of the QA Analytics & Aseptics Team in QA Operations that is responsible for the final overall quality oversight of the production, Quality Control and other operational units within Stein C & GT manufacturing. The QA Operations team ensures that the quality strategy is implemented and that there is a continuous drive to improve product and process quality within the operational units. Your responsibilities: Your responsibilities include, but are not limited to: • QA Oversight of CGT Quality Control (QC) Unit. This includes QA for release analytics of media and finished product, e.g. FACS, qPCR, ELISA, beads and virus analytics. • QA Oversight of CGT Manufacturing Unit/shopfloor with regard to aseptic topics, e.g. hygiene, aseptic working technique, environmental monitoring, best practice in clean rooms. • Writing, review and/or approval of validation and qualification documents (plans and reports), Out of Specification records, Deviations and other Quality Events, Change Requests, SOPs, risk assessments, testing monographs, transfer documents, lab protocols, trending reports, annual reports, stability reports, certificate of analysis (CoA). • Be point of contact regarding QA questions in quality control and aseptic questions in manufacturing unit, provide ad hoc decisions and act as trainer and advisor on aforementioned topics. • Participate and key person in health authority and internal inspections. Minimum requirements What you’ll bring to the role: • 2-5 years of GMP/GxP experience in pharmaceutical QC, QA, MS&T or production environment, preferably in sterile manufacturing or Cell & Gene (ATMPs) • Strong knowledge and expertise in Quality Control and Aseptics • Strong written and verbal communication skills, ability to communicate clearly with a variety of individuals in various aspects of Novartis operations (QA, QC, PU, MS&T, Logistics) • IT-Knowledge (MS Office, SAP, Outlook, Trackwise, LIMS) Desirable requirements: • BA or MS in Cell/Molecular Biology, Genetics, Biochemistry, Microbiology or related discipline • Fluent in German, good working knowledge in English Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.We are Novartis. Join us and help us reimagine medicine.DivisionNovartis Technical OperationsBusiness UnitNTO QUALITYLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeRegularShift WorkYes Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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22.07.2020

Novartis AG

Bio-Laborant / Cell Processing Specialist

  • Novartis AG

  • 4332Stein (Säckingen)

  • 22.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID299393BRPosition TitleBio-Laborant / Cell Processing SpecialistApply to Job Job Description 10 days! That is how long we treat a patient’s T-cells, before we return them to potentially save this patient’s live. To support such novel, personalized treatment by working with the patient’s own cells in our production process, is a unique challenge within Novartis with immediate patient impact. The Cell Processing Specialist CGT is responsible for all production days of our manufacturing process of patient derived clinical and commercial cellular immunotherapy products. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation. Your responsibilities include, but are not limited to: • Ownership for processing of the assigned patient starting material in the clean room environment • Ability to gown aseptically and work in clean room environment for extended periods of time, ability to work with automated equipment such as the Cell Saver CS5 and Sepax, preparing needed equipment, verification of intermediate process days (expertise with wave bioreactor, NC-200 Cell Counter and in process environmental monitoring) • Electronical documentation of all steps in assigned batch record in line with GMP (good manufacturing practices) requirements & conduction of all necessary processing/verification steps for the assigned lot (and media) with highest skill level of aseptic technique • Assistance on deviation investigations and inspections & participation as well as assigned qualification/validation activities • Perform other duties as assigned; ie. batch record review, process streamline improvements, safety walk-throughs Minimum requirements What you’ll bring to the role: • Studies/Apprenticeship in relevant Scientific discipline (e.g. MTA / PTA, Biotechnology, Biology or Laboratory Assistant or Engineering) and ideally 1 year experience in cGMP or academic or lab setting with aseptic or cell culture experience • Fluent in German & good understanding of English • Experience in cell therapy manufacturing preferred (desired in Aseptic processing in ISO 5 biosafety cabinets, universal precautions for handling human derived materials in BSL-2 containment areas, Cell expansion using incubators and single use bioreactors, Cell automated equipment, Knowledge of cGMP regulations and FDA guidance) • Ability to work in different shifts (also weekend), ability work with magnetic field equipment and requires handling of chemicals / biohazardous materials • Ability to cooperate with other groups / Teams / DepartmentsDivisionNovartis Technical OperationsBusiness UnitNTO CELL & GENE THERAPYLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaTechnical OperationsJob TypeFull TimeEmployment TypeTemporaryShift WorkYes Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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21.07.2020

Novartis AG

Prozessmitarbeiter

  • Novartis AG

  • 9655Stein (Säckingen)

  • 21.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID297516BRPosition TitleProzessmitarbeiterApply to Job Job Description 150! Unser Werk Novartis Stein Steriles ist einer der wichtigsten Standorte für innovative, hochqualitative, sterile Medikamente, die wir jeden Tag für unsere Patienten in über 150 Ländern produzieren und verpacken. Um die Abteilung Novartis Technical Operations zu verstärken, suchen wir per sofort 2 Prozessmitarbeiter für jeweils 24 Monate. Hauptaufgaben: • Isolator Vorbereitung für Produktion • Integritätsprüfungen von Belüftungs- /und Produktfiltern • Reinigungen und Desinfektionen aller Art (Anlagen und Umgebung) • Support des Mechanikers bei Formatwechsel der Anlage • cGMP Dokumentation der durchgeführten Prozesse • Bedienen der Vialwaschmaschine • Durchführen von CIP (Cleaning in Place) und SIP (Sterilizing in Place) Minimum requirements • Reinraum-Qualifizierung oder abgeschlossene Berufslehre als Chemie- und Pharmatechnologe oder ähnliches oder langjährige, einschlägige Berufserfahrung in der Chemie- oder Pharmabranche • gute Deutschkenntnisse in Wort und Schrift ( Englischkenntnisse von Vorteil) Warum Novartis? 750 Millionen - so viele Menschen haben wir mit unseren Produkten erreicht. Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. Wir sind Novartis. Kommen Sie zu uns und denken Sie Medizin mit uns neu.DivisionNovartis Technical OperationsBusiness UnitNTO ASEPTICSLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaTechnical OperationsJob TypeFull TimeEmployment TypeTemporaryShift WorkYes Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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09.07.2020

Novartis AG

Postgraduate PU Galenik

  • Novartis AG

  • 4332Stein (Säckingen)

  • 09.07.2020

  • Vollzeitstelle

Back to Previous Page Job ID298678BRPosition TitlePostgraduate PU GalenikApply to Job Job Description 80Millionen! Das ist die Anzahl der sterilen Produkte, die in unserem Arbeitsplatz pro Jahr verarbeitet werden. Als Teil des Teams für die Produktion spielen Sie eine Schlüsselrolle bei der Herstellung und Sicherstellung der höchsten Produktqualität für Millionen von Patienten in mehr als 150 Ländern auf der ganzen Welt. Für die Process Unit (PU) Galenic suchen wir ab sofort einen motivierten und engagierten Postdoc / Postgraduate für 12 Monate der einen Einblick in die Rolle des Prozessexperten in der sterilen Produktion erhalten und uns aktiv unterstützen möchte. Aufgaben - Unterstützung bei Untersuchung und Bearbeitung von Herstellabweichungen (Deviations) und dem CAPA-Management - Identifikation von Prozessschwachstellen und Mithilfe bei Projekten zur Prozessverbesserung - Erstellung und Update von SOPs - Update von Herstellungsdokumenten - Mithilfe bei der Planung und Durchführung von Reinigungsvalidierung und thermischer Requalifizierung - Mithilfe bei der Dokumentationsvorbereitung und Bearbeitung von Risiko Analyse und Änderungsanträge (Change Request) - Erstellung von Dokumentationen und Testberichten - Unterstützung bei der Mitarbeiterqualifizierung Minimum requirements Mindestanforderungen - Naturwissenschaftliches oder Pharmazeutisches Studium - Gute Englisch- und Deutschkenntnisse - Sie sind für ein Studium (Bachelor/Master) eingeschrieben oder haben dieses gerade (vor maximal 12 Monaten) abgeschlossen - Teamfähigkeit und Flexibilität - Offene Kommunikation und Engagement Warum Novartis? 750 Millionen - so viele Menschen haben wir mit unseren Produkten erreicht. Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. Wir sind Novartis. Kommen Sie zu uns und erfinden Sie Medizin mit uns neu.DivisionNovartis Technical OperationsBusiness UnitNTO ASEPTICSLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
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