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Altran Switzerland AG

Die ALTRAN Gruppe wurde im Jahr 1982 gegründet und ist heute in Europa der Marktführer für Innovations- und Hightech-Consulting. Altran hat es sich zur Aufgabe gemacht, seine Kunden bei der Schaffung und Entwicklung neuer Produkte und Serviceleistungen zu unterstützen.

Altran beschäftigt in der Schweiz mehr als 200 Berater. Sie sind in den meisten Branchen tätig und konzentrieren sich insbesondere auf den öffentlichen Dienst, das Gesundheitswesen, Transportwesen und Luftfahrt, die Industrie und den Telekommunikationsbereich. Altran Switzerland hat Büros in Lausanne, Genf, Zürich und Basel. Altran arbeitet mit den Unternehmen während sämtlicher Phasen des Innovationsprozesses zusammen, welche unter anderem die Technologiefrühaufklärung, angewandte Grundlagenforschung, Managementberatung, Industrial Systems Engineering sowie Informationssysteme einschließlich systematischer Ideation, Technologiestrategie, F&E und Produktion umfassen. Der Konzern beschäftigt weltweit 23'000 Berater, die zusammen sämtliche Engineering-Bereiche vereinen und in vier Hauptgeschäftsbereichen tätig sind: Technologie- und F&E-Beratung; Beratung für Organisations- und Informationssysteme; Strategie- und Managementberatung sowie Schulungslösungen für Unternehmen unter der Marke Altran Education Services. Altran ist seit 2003 offizieller Partner des inspirierenden Abenteuers Solar Impulse.

Altran Switzerland AG

Hardturmstrasse 253
8005Zürich

07.04.2020

Altran Switzerland AG

Packaging Engineer

  • Altran Switzerland AG

  • 4051Basel

  • 07.04.2020

  • Vollzeitstelle

Job TitleVerpackungsingenieur/in Vacancy Reference Number22620 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypeUnbefristet [Vollzeit] Minimum number of years of experience required2 years of experience and more Our offer Internationale Unternehmenskultur mit über 50‘000 Kollegen in mehr als 30 Ländern Attraktives, mehrstufiges Karrieremodell mit Spezialisierungsmöglichkeiten Interessante Entwicklungschancen in einem dynamischen Unternehmen mit flachen Hierarchien Fach-, Methoden- und Softskilltrainings an der Altran Academy Angenehme, teamgeprägte Arbeitsatmosphäre mit regelmässigen Community Events Ein anspruchsvolles Aufgabengebiet mit hoher Eigenverantwortung und abwechslungsreichen Projekten (in der Deutschschweiz) Your role Bestehende Betriebsanlagen und Infrastrukturen unterstützen Planung, Optimierung und Umsetzung von Projekten Auswertung, Entwicklung und Durchführung von Prozessabläufen nach Lean-Vorgaben Zusammenstellung und Ausführung von kunden, kosten- und prozessoptimisierten Konzeptionen in Übereinstimmung mit den Betriebsanforderungen Kundenbetreuung Ausarbeitung von Projekt- und Anlagendokumentation Your profile Abschluss im technischen Bereich mit Schwerpunkt Verfahrenstechnik oder Anlagenbau Mindestens 3 bis 5 Jahre Erfahrung im GMP oder in einem stark regulierten Umfeld Fliessende Deutsch- und Englischkenntnisse Sehr gute MS Office und G-Suit Kenntnisse Exakte Arbeitsweise und Zuverlässigkeit auch unter zeitlicher Belastung Kommunikativ,Qualitätorientiert und Teamplayer
Inserat ansehen

07.04.2020

Altran Switzerland AG

Quality Expert for Medical Devices

  • Altran Switzerland AG

  • 4040Basel

  • 07.04.2020

  • Vollzeitstelle

Job TitleQuality Expert for Medical Devices Vacancy Reference Number22624 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting. A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role The Quality Expert Medical Device has to ensure technical development of assigned Medical Device/Combination Product Projects are conducted in accordance with Design Control requirements per Quality System, ensuring regulatory compliance and safe and effective use.   Provide quality and compliance expertise in the area of responsibility for medical devices and combination products Manage assigned projects and activities and ensure regulatory compliance, with a specific focus on design control aspects Ensure GMP compliance by review and approval of deliverables (e.g. procedures, records) as well as monitoring analysis and reporting of GMP related KPIs Manage quality problems (non-conformities, out-of-specifications, complaints) and technical matters and ensure they are resolved consistently, in a timely manner and in accordance with global standards and policies Your profile Graduate in Chemistry, Pharmacy, Microbiology or Biotechnology or another related science At least 2 years of relevant experience in design control Sound knowledge in medical device or combination product regulations, standards and guidelines Very good knowledge of medical device development or life-cycle management Ability to influence people, negotiate and communicate Excellent knowledge of cGMP and GMP compliance
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06.04.2020

Altran Switzerland AG

Packaging Engineer

  • Altran Switzerland AG

  • 4051Basel

  • 06.04.2020

  • Vollzeitstelle

Job TitlePackaging Engineer Vacancy Reference Number22619 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Part-Time] Minimum number of years of experience required2 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva Your role Support existing facilities and infrastructure Planning, steering and completion of projects Analysis, development and realization of process flows taking lean approaches into consideration Develop and implement customer-focused, cost and process efficient concepts Customer support Develop project and plant documentation Your profile Degree in a technical field with focus on process or plant engineering At least 3 to 5 years of experience in GMP or strongly regulated environment Strong MS Office and G-Suit skills Fluent in English and German Ability to work precisely and reliably even under time constraints Team-player, quality oriented and communicative person
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06.04.2020

Altran Switzerland AG

Cell and Gene Therapy Consultant

  • Altran Switzerland AG

  • 4040Basel

  • 06.04.2020

  • Vollzeitstelle

Job TitleCell and Gene Therapy Consultant Vacancy Reference Number22622 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer   A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Improve CGT processes and support scaling of production (process optimization, automation, etc.) Provide scientific and technical guidance in clinical and product development Support the client in working with cross-functional teams of molecular biologists, data scientists and bioprocess / automation engineers Support GMP/GTP as well as regulatory compliance in the area of cell, gene and tissue therapies Your profile PhD in molecular biology, cellular biology, stem cell biology, biomedical engineering or related fields within biological cellular systems 5+ years of relevant experience within the biotechnology/ pharmaceutical industry or clinical laboratories preferably with an oncology background Strongprocess expertise inpharmaceutical production (cell & gene therapy) - from upstream, viral vector generation, to downstream, purification and recovery of the final viral product Technical skills in pre-clinical, clinical and commercial production for cell therapy biopharmaceuticals and proteins Excellent verbal and written communication skills as well as excellent time management and organizational skills Ability to generate new ideas, achieve results and solve problems Fluent in English (German & French is an advantage) Further beneficial competencies include: Six Sigma Green/ Black Belt Experience in technology transfer Practical competencies in cell or gene therapy technologies (e.g. viral delivery systems, upstream & purification systems, bioprocessing) Working knowledge of Supply Chain Management as well as commercialisation and reimbursement strategies for CGT   If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful. Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland. Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities.    
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05.04.2020

Altran Switzerland AG

Quality Engineer for Consumable Product

  • Altran Switzerland AG

  • 4040Basel

  • 05.04.2020

  • Vollzeitstelle

Job TitleQuality Engineer for Consumable Product Vacancy Reference Number22607 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva Your role Monitoring, quality assurance and carrying out the technical release of the assigned products Subject matter expert for manufacturing processes and technical expertise for testing processes Deviation and CAPA Management, Change Control Management Elaboration and preparation of test plans for new plants and development projects Implementation, preparation and interpretation of test data sets, Maintenance of the test specification documents and instructions, including training Creation and processing of deviation reports, as well as support for customer complaints Equipment owner of various test systems Evaluation of new test methods equipment and life-cycle support up to series release Planning of tests and coordination of their execution Continuous process improvement Your profile Bachelor’s degree / Master’s degree in medical technology / scientific / technical direction or any related field Advanced training or experience in the field of quality assurance, quality engineering, test planning, and Six Sigma methodology In-depth IT knowledge (MS Office, MiniTab, JMP, SAP) Practical experience in a regulated environment, ideally in medical device or in vitro diagnostics (ISO e13458, GMP, FDA 21 CFR 820) Very good communication skills in German and English Application experience with FMEAs, MSAs and statistical process controls Experience in complaint and deviation reporting handling (8D method)
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05.04.2020

Altran Switzerland AG

Quality Engineer for Consumable Product

  • Altran Switzerland AG

  • 4040Basel

  • 05.04.2020

  • Vollzeitstelle

Job TitleQuality Engineer for Consumable Product Vacancy Reference Number22608 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva Your role Überwachung und Gewährleistung der Qualität der zugewiesenen Produkte, sowie Durchführung der fachlichen Freigabe der zugewiesenen Produkte Wissensträger über Herstellprozess und Fachspezialist der Prüfprozesse Bearbeitung von Change-Tasks / CAPA-Tasks Ausarbeitung und Erstellung von Prüfplänen für neue Anlagen und Entwicklungsprojekte Durchführung der Prüfdatenerhebung, -aufbereitung und -interpretation Instandhaltung der Prüf-Vorgabedokumente und -Anweisungen inkl. Schulungen Erstellung und Bearbeitung der Abweichungsmeldungen, sowie Unterstützen bei Kundenbeanstandungen Prüfmitteleigner von Prüfsystemen Evaluierung von neuen Prüfmethoden und Prüfmittel und Begleiten dessen zur Serienreife Planung von Prüfungen und Koordination von dessen Durchführung Kontinuierliche Verbesserung von Prozessen Your profile Hochschul- oder Fachhochschulabschluss in Medizintechnik / naturwissenschaftlicher / technischer Richtung oder eine technische Grundausbildung (EFZ) mit mindestens drei Jahren praktischer Erfahrung im Qualitätswesen oder im diagnostischen / molekularbiologischen Labor von Vorteil Weiterbildung oder Erfahrung im Bereich Quality Assurance, Qualitätstechnik, Prüfplanung, sowie Six Sigma-Methodik Vertiefte EDV Kenntnisse (MS Office, MiniTab, JMP, SAP) Praxiserfahrung in einem regulierten Umfeld, idealerweise in der Medizinaltechnik oder invitro diagnostics (ISO e13458, GMP, FDA 21 CFR 820) Konversationssicher in Deutsch und Englisch Anwendungserfahrung mit FMEAs, MSAs und statistischen Prozesskontrollen Erfahrung in der Complaint- und Abweichungsmeldung-Handhabung (8D Methode)
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02.04.2020

Altran Switzerland AG

TMF Manager Outsourced Studies

  • Altran Switzerland AG

  • 4051Basel

  • 02.04.2020

  • Vollzeitstelle

Job TitleTMF Manager Outsourced Studies Vacancy Reference Number22587 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Manage the Trial Master Files (TMFs) and other TMF related (migration), inspection-relevant documents. Supervise the process, system and tool landscape that supports the management of outsourced TMFs. Promote best documentation practice and provide guidance on document standards to support inspection readiness and adherence to Good Documentation Practice / Good Clinical Practices. Create and/or update SOPs, Working Practices, Guidance Documents, templates, etc. Enforce the use of standards and adherence to quality, by providing training and support to business functions in cooperation with TMF QC Manager. Work as Business Administrator in the electronic Document Management System (eDMS). Act as Business Lead to manage the implementation of a Next Generation DMS. Your profile Bachelor’s Degree in Life Science/Healthcare or equivalent. At least 5 years working experience in clinical development/clinical operations. At least 3 years working experience with document management systems. Excellent understanding of system structures and generic document management functionality. Thorough knowledge of clinical Trial Master File process, regulations and Good Clinical Practice. Advanced knowledge of clinical documentation and reporting. Knowledge of the national and international data protection legislation. Fluent English (oral and written), German of advantage.   If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful. Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland. Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities.
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02.04.2020

Altran Switzerland AG

Project Quality Manager (QAM)

  • Altran Switzerland AG

  • 4040Basel

  • 02.04.2020

  • Vollzeitstelle

Job TitleProject Quality Manager (QAM) Vacancy Reference Number22589 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting. A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Management of Change Controls (Agile). Preparation and alignment of Quality Assurance Agreement (QAA). Review and approval of Master Batch Records, validation protocols & reports, Quality Risk Assessments, Testing Monographs etc. Management of Deviations / OOS results (TrackWise/AQWA). Assuring cGMP compliance of DS manufacturing, testing and release. Your profile Bachelor or higher degree in Biochemistry, Chemistry, Microbiology or other related science. Minimum 3 years of experience in in the pharmaceutical industry. Minimum 3 years of experience in operational quality assurance. Good knowledge of cGMP requirements for major regulated markets (EU, US). Project work experience required. Experience with IT tools like Trackwise (AQWA), Subway, Agile desirable.
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01.04.2020

Altran Switzerland AG

SAP Expert

  • Altran Switzerland AG

  • 4040Basel

  • 01.04.2020

  • Vollzeitstelle

Job TitleSAP Expert Vacancy Reference Number22577 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting. A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Assessing new or modified requirements with respect to technical feasibility and complexity and the impact on current and planned systems, standards and guidelines (requirements engineering). Defining required technical resources, software architecture, user interface, and database system. Creating or selecting the most suitable methods, techniques, standards, guidelines, and tools for software development. Assessing software solutions from the perspectives of security risk, implementing and executing the required procedures for risk analysis in software systems. Analysis of problems, providing third level support, definition and implementation of the escalation procedures. Your profile 2-3y of experience in the development and support of SAP Analytics Cloud modeling.  5y+ SAP experience and understanding of a full software development lifecycle.  Solid understanding of software components and architecture, especially limitation of data blending, when to use data replication or live connection.  Knowledge of JavaScript and CSS for Application Designer.  Knowledge of OData for data replication. 
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01.04.2020

Altran Switzerland AG

Consumables Manager

  • Altran Switzerland AG

  • 4040Basel

  • 01.04.2020

  • Vollzeitstelle

Job TitleConsumables Manager Vacancy Reference Number22573 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Acting as point of contact for Regulatory when supporting country specific registrations with additional documentation Budgeting for Standard Manufacturing Cost, one time period cost and Product Care activities Initiating product care projects as sponsor for invest projects, process and product improvement projects and obsolescence projects Responsible for evaluation of change requests from suppliers and other organizations Acting as Consumables representative in instrument Product Team Meetings, System Development organization and Product Care Quality Teams related to the Consumables portfolio Your profile Completed university studies (e.g. mechanical engineering, automation technology/materials engineering) or comparable higher education in a technical and analytical field with experience in the medical field, especially in in-vitro diagnostics Experience in regulated product development in cooperation with international stakeholders Experience in project management with external partners/suppliers Technical manufacturing experience with high level of automation German and English - Proficient
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01.04.2020

Altran Switzerland AG

Project Manager (IT)

  • Altran Switzerland AG

  • 4040Basel

  • 01.04.2020

  • Vollzeitstelle

Job TitleProject Manager (IT) Vacancy Reference Number22575 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting. A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Define, plan, and direct the execution of a broad range of projects while balancing the competing demands of scope, time, cost, quality, resources, and risk to produce high IT solutions. Manage relationships with various IT and business stakeholders to achieve project objectives. Plan, baseline and control costs to ensure projects are completed within approved budget. Identify and apply systematic quality activities to ensure that projects employ all processes needed to meet Computer System Validation directives. Conduct risk and issue management planning, identification, analysis and monitoring on projects. Your profile 8y+ of experience implementing IT Projects across a variety of platforms in a similar environment (Pharmaceutical / Diagnostics, Healthcare). Agile practitioner with proven knowledge of Scrum / SAFe principles and PMP certification.  Proven Organizational Change Management experience. Strong understanding of Computer System Validation (CSV) concepts / familiarity with HP ALM or other Application Lifecycle Management.  Proven experience in leading virtual off-shore teams. 
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30.03.2020

Altran Switzerland AG

Project Manager Life Sciences

  • Altran Switzerland AG

  • 4051Basel

  • 30.03.2020

  • Vollzeitstelle

Job TitleProject Manager Life Sciences Vacancy Reference Number11101 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Altran deploys its expertise particularly in: Life Sciences (Pharma, Biotech, and Medical Devices), Industry, Aerospace, Automotive, Energy, Railways, Financial Services: P&C Insurance, Health Insurance, Reinsurance, Banking Telecoms Public sector Your role Consulting, designing and implementing the overall PMO organizational structure, relevant processes, tools and templates Providing project management and PMO process support to Leadership and Project Managers. Affording guidance and training for the tools and methodology implemented Identifying issues occurring across projects and programs and improve them Communicating portfolio priorities and furnishing information about the state of current investment Working with the functional managers and/or segment managers to scope the overall project roadmap Managing project time & cost management to achieve timeline and budget, ensuring cost and risk reduction goals Your profile MSc / PhD in Project Management, IT, or Business Administration. PMP, PMI, PRINCE2 Certification required Knowledge of the drug development process relevant to Pharmaceutical / Biotech industry (minimum of 5 years' experience preferred) You have at least 5 years of extensive experience in Project Management Experience in the successful creation of a PMO Experience working in cross functional project teams You have strong communication skills and can present your ideas in a team Languages : English fluent and German is a plus
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30.03.2020

Altran Switzerland AG

Medical Devices Development Specialist

  • Altran Switzerland AG

  • 4051Basel

  • 30.03.2020

  • Vollzeitstelle

Job TitleMedical Devices Development Specialist Vacancy Reference Number11099 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Altran deploys its expertise particularly in: Life Sciences (Pharma, Biotech, and Medical Devices), Industry, Aerospace, Automotive, Energy, Railways, Financial Services: P&C Insurance, Health Insurance, Reinsurance, Banking Telecoms Public sector Your role Deliver project according to planned timelines, resource and budget; Plan and lead technical activities; Manage technical development activities in collaboration with internal stakeholders as well as in the projects teams; Lead the collaboration with external development partners; Monitor work progress according to plan; Monitor, support and challenge technical development as well as test and verification work; Monitor development and implementation of manufacturing processes; Coordinate and monitor technical documentation. Your profile MSc degree in Science/Engineering or Mechanical Engineering Experience in leading devices / combination product projects Good understanding of Medical Device Regulations (ISO 13485, EU Medical Device Directive) Experience in Product design and Design for manufacture Experience of managing external suppliers Good technical knowledge of primary containers development General understanding of Human Factors Engineering and Risk management Good understanding of pharmaceutical development in general Languages:  English fluent and German is clearly a plus
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30.03.2020

Altran Switzerland AG

Packaging Device Engineer - Pharma

  • Altran Switzerland AG

  • 4051Basel

  • 30.03.2020

  • Vollzeitstelle

Job TitlePackaging Device Engineer - Pharma Vacancy Reference Number11100 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Altran deploys its expertise particularly in: Life Sciences (Pharma, Biotech, and Medical Devices), Industry, Aerospace, Automotive, Energy, Railways, Financial Services: P&C Insurance, Health Insurance, Reinsurance, Banking Telecoms Public sector Your role Leading the definition of product requirements for packaging, medical devices, delivery systems, e.g. drug/device combination products in which the device is generally already registered but sometimes to be developed Provide primary packaging and device expertise in a broader cross-functional drug product development team Supporting and coordinating the manufacturing of clinical material and the production scale up Managing and monitoring Human Factors Engineering activities Leading Risk management activities Planning and monitoring of design verification activities (in-house) Ensuring a high quality Design History file Your profile MSc degree in Packaging Science/Engineering An ideal candidate would have a relevant degree in engineering and at least 7 years’ experience in leading device development technical teams in a similar area Understanding of medical device regulations (FDA 21CFR 820, FDA 21CFR Part 4, EU Medical Device Directive, EU Medical Device Regulation) Development and writing of technical documentation of drug/device combination products and medical devices, including Design Control process and other applicable regulatory, QA and GMP aspects Experience with Design Control, ISO1345, Primary Pharmaceutical Packaging Development, ideally for combination products is important. Fluent in English and German is clearly a plus
Inserat ansehen

30.03.2020

Altran Switzerland AG

QA/RA Med Tech - New MDR

  • Altran Switzerland AG

  • 4040Basel

  • 30.03.2020

  • Vollzeitstelle

Job TitleQA/RA Med Tech – New MDR Vacancy Reference Number11102 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Altran deploys its expertise particularly in: Life Sciences (Pharma, Biotech, and Medical Devices), Industry, Aerospace, Automotive, Energy, Railways, Financial Services: P&C Insurance, Health Insurance, Reinsurance, Banking Telecoms Public sector Your role Participate on (MDR implementation) by representing and reinforcing, Quality Assurance and Regulatory Affairs requirements Work in a multidisciplinary group for Technical File adaption according to MDR 2017/745 Ensure that the technical documentation supporting the CE mark complies with MDD 93/42/EEC Create and maintain Technical Files/Design Dossiers Support the International Regulatory Affairs Team in preparation of International Submissions Interaction with authorities, notified bodies and any other approving bodies that will be relevant Assessment of potential risks and the classification of the medical device in accordance with MDD and MDR Support and consultation of the Departments in regard of interpretation of regulatory rules/laws/guidelines Your profile MSc/PhD degree in Pharmacy, Regulatory field Minimum 5 years of professional experience in Regulatory Affairs and/or Quality Management Detailed knowledge about the standards and directives for Medical Devices such as ISO 13485 , ISO 14971, MDD 93/42/EEC and MDR 2017/745 Experience from Audits would be a plus Advanced knowledge of excel and data analysis would be a plus Fluency in English, German would be an asset
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30.03.2020

Altran Switzerland AG

Quality Manager Med Tech

  • Altran Switzerland AG

  • 4051Basel

  • 30.03.2020

  • Vollzeitstelle

Job TitleQuality Manager Med Tech Vacancy Reference Number11106 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Altran deploys its expertise particularly in: Life Sciences (Pharma, Biotech, and Medical Devices), Industry, Aerospace, Automotive, Energy, Railways, Financial Services: P&C Insurance, Health Insurance, Reinsurance, Banking Telecoms Public sector Your role Be aware about new Medical Devices Regulations 'MDR' Lead dedicated team efforts, e.g. regulatory submissions preparation, root cause analysis, new regulation/standard task force. Collaborate actively on the development of combination products and on design transfers. Ensure continued alignment with Regulatory Affairs teams (global and local) requirements and planning. Ensure continued alignment with Legal teams (global and local) requirements, strategies and planning. Your profile PhD, Master Degree in Pharmacist or in Quality Engineering Min 5 years of experience as QA/RA manager in the medical devices industry (focus on complex medical electrical equipment, including HW, SW and mechanics) with cross functional experience in international environment. Strong experience in matter of quality assurance/regulatory affairs (class I, IIB). Excellent knowledge of ISO13485, 21 CFR 820, ISO 14971. Excellent knowledge of medical device regulations, CE marking, 510 (k), 21 CFR 4 for combination products. Knowledge of electrical and software development standards (IEC 60601-1, IEC 62304) and of the radio-communication regulations (1999/9/EC, 47 CFR) is a plus. Languages : English fluent & German is clearly a plus
Inserat ansehen

30.03.2020

Altran Switzerland AG

IT - CSV Engineer

  • Altran Switzerland AG

  • 4040Basel

  • 30.03.2020

  • Vollzeitstelle

Job TitleIT - CSV Engineer Vacancy Reference Number11098 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Altran deploys its expertise particularly in: Life Sciences (Pharma, Biotech, and Medical Devices), Industry, Aerospace, Automotive, Energy, Railways, Financial Services: P&C Insurance, Health Insurance, Reinsurance, Banking Telecoms Public sector Your role Lead validation activities of Computerized Systems in the Life Sciences Industry Assist in maintaining equipment automation systems in a validated state as they relate to GxP CSV automation systems. Execute QA reviews and approvals of IT SOPs, and validate master plans for computerized system implementations. Develop an appropriate document control capability and ensure all documents filings and archiving systems are accurate, up to date and maintained in accordance with GMP and other relevant regulations. Establish and ensure good and close working relationship with important project stakeholders and internal customers. Your profile MSc Degree in engineering, IT, Science or Computer related discipline. 5 years proven track record in Computer System Validation in Pharmaceutical or Life Science environment. Strong project management skills with the ability to prioritize assignments Familiar with GxP systems. Fluent knowledge of GAMP 5, Annex 11, CFR Part 11 Compliance and CFR Part 210, 211 & 820 compliance. Excellent analytical and problem solving skills. Languages: English fluent and German is a plus
Inserat ansehen

30.03.2020

Altran Switzerland AG

Clinical Development Director (CDD)

  • Altran Switzerland AG

  • 4040Basel

  • 30.03.2020

  • Vollzeitstelle

Job TitleClinical Development Director (CDD) Vacancy Reference Number21184 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting. A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Provides clinical leadership and strategic input for all clinical deliverables in the assigned project or section of a clinical program. Leads development of clinical sections of trial and program level regulatory documents. Oversees ongoing medical and scientific review of clinical trial data with Clinical Scientific Expert(s) with appropriate oversight from Medical Lead. Supports the interactions with external stakeholders (e.g. regulatory authorities, key opinion leaders, data monitoring boards, advisory boards, patient advocacy groups) and internal decision boards. Serves on or leading global initiatives (e.g. process improvement, training, SOP development, other Clinical Development line function initiatives). Contributes to scientific training of relevant stakeholders on the disease area and compound/molecule. Your profile Advanced degree in life sciences/healthcare relevant degree is required. PharmD, or PhD strongly preferred. More than 5 years of involvement in clinical research, clinical trials or drug development. Advanced knowledge of assigned therapeutic area. Thorough knowledge of GCP, clinical trial design, statistical analysis methodology, and regulatory/clinical development process. Demonstrated ability to establish strong scientific partnership with key stakeholders. People management experience. Excellent interpersonal, communication, negotiation and conflict resolution skills. Fluent oral and written English. If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful. Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland.   Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities.
Inserat ansehen

29.03.2020

Altran Switzerland AG

Medical Device Regulatory Affairs Manager

  • Altran Switzerland AG

  • 4051Basel

  • 29.03.2020

  • Vollzeitstelle

Job TitleMedical Device Regulatory Affairs Manager Vacancy Reference Number20918 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Develop, implement, communicate, and maintain global regulatory strategies and plans for devices Identify and communicate relevant guidance, policies, standards, and regulations Assist the review of product and process documentation for assigned projects to ensure compliance with change control requirements to aid in determining if regulatory submissions are required Creation, review and maintenance of regulatory related technical documentation Work with cross-functional teams to obtain relevant information and subsequent review of submission content as needed; assist in review of international product technical documents, marketing and labeling materials Support the maintenance of regulatory files and tracking databases to ensure prompt and accurate access to company regulatory information concerning current, pending, and future approvals and renewals Perform change management assessments; determine and communicate post-approval reporting requirements Your profile Masters degree in Regulatory Affairs, Life Sciences, or Engineering Minimum 3-5 years of experience in European Medical Device industry especially with regulatory, quality or engineering  Strong knowledge of ISO 13485 and ISO 9001, QSR  and Medical Devices applicable requirements, especially Council Directive 93/42/EEC and Regulation 2017/745, as they pertain to technical documentation Strong understanding of Risk Management process, label and labeling, change management is desired                
Inserat ansehen

29.03.2020

Altran Switzerland AG

Project - Program Manager Life Sciences

  • Altran Switzerland AG

  • 4040Basel

  • 29.03.2020

  • Vollzeitstelle

Job TitleProject - Program Manager Life Sciences Vacancy Reference Number22063 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer Altran is the global leader in Innovation, Digital and High-tech engineering consulting. At Altran, you get the chance to work on projects among a multi disciplinal portfolio and you become part of our international community of like-minded experts!  Our Life Sciences Division in Switzerland is providing Digital and Engineering services from the conception, through development, quality assurance and transfer to production, implementation, and rollout.  We are proud to collaborate with the major players of the MedTech, Biotech and Pharmaceutical sectors to strengthen their market share. Follow your passion in a role where you will be exposed to the technologies and processes that leading global companies utilize, and join our innovative team as Project - Program Manager Life Sciences. Your role Designing and implementing the overall PMO organizational structure, relevant processes, tools and templates. Developing and driving integrated project plans, aligning project tactics with network strategy. Affording guidance and training for the tools and methodology implemented. Recognising and improving issues occurring across projects and programs. Designing in the definition of project scope and objectives, involving all relevant stakeholders and ensuring technical feasibility. Communicating portfolio priorities and furnishing information about the state of current investment. Working with the functional managers and/or segment managers to scope the overall project roadmap. Developing and tracking resource planning, managing project time & cost management to achieve timeline and budget, ensuring cost and risk reduction goals. Your profile 3.MSc / PhD in Project Management, IT, or Business Administration. PMP, PMI, PRINCE2 Certification required. Knowledge processes relevant to Pharmaceutical / Biotech industry (minimum of 5 years' effective and extensive project management experience). Experience in the successful creation and of a PMO. Experience in working with cross functional project teams. Excellent organisational skills. Excellent written / oral communication, facilitation and presentation skills. Proven ability to create strong working relationships with respect to cultural diversity and working styles. Effective decision-making skills and ability to identify issues requiring appropriate escalation. Ability to translate complex concepts into actionable, measurable tasks. English fluent written and spoken and German is a plus. If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful. Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland.   Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities.   Our offer: A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva.
Inserat ansehen

29.03.2020

Altran Switzerland AG

Clinical Trial Leader

  • Altran Switzerland AG

  • 4040Basel

  • 29.03.2020

  • Vollzeitstelle

Job TitleClinical Trial Leader Vacancy Reference Number20473 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Responsible for the management and clinical execution of clinical trials. Functions as the CTL on the planning and implementation of all operational aspects of assigned TM clinical trials, from study concept to reporting. Collaborates with the Medical Expert and CTT, coordinate the ongoing medical / scientific review of the clinical trial data, the data analysis and interpretation. Leads the study planning in collaboration with outsourcing personnel, CTT members, Local Country Office representatives and CRAs, identify sites and manage study set-up and organize the Investigator meetings. Being the author of the clinical study protocol and ensure a complete review of all study documentation is conducted within the assigned studies. Maintain the knowledge and training of ICH-GCP, current regulations and procedures and supplement by training and practice of SOPs and internal policies. Manages the clinical trial materials, including drug supplies and CRFs. Your profile BSc, MSc or PhD level in life sciences/healthcare. 5 years relevant experience in clinical trials / drug development. Good knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process. Recent Respiratory experience. Track record of successfully managing multiple, concurrent phase I and II clinical trials. Hands-on experience in patient data review, cleaning and analysis recommended. Fluent English (oral and written). If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful. Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland. Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities.
Inserat ansehen

29.03.2020

Altran Switzerland AG

UX/UI Designer

  • Altran Switzerland AG

  • 4051Basel

  • 29.03.2020

  • Vollzeitstelle

Job TitleUX/UI Designer Vacancy Reference Number22077 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva Your role Imagination and creativity will be your day-to-day tools to invent tomorrow’s products and interfaces. Together with our clients, we work at finding the best and most attractive solutions answering their needs, through a unique problem solving co-creation approach We are looking for new colleagues with curious minds, able to work in a multidisciplinary team and to manage multitasking. Within the team, you will have the opportunity to practice or to sharpen your knowledge in design thinking, cognitive ergonomics, creative problem solving in a dynamic and enthusiastic work environment Your profile You have 2-6 years’ experience in interaction design and you master the design tools or you can showcase relevant skills (portfolio) (Adobe Suite / Sketch) You know how to prototype your ideas in a “quick and dirty“ manner (Marvel / Invision / Balsamiq) Your area of expertise is interaction design (UX / UI) but you are also open to other disciplines such as product design or motion design Programming (HMTL / CSS / Arduino / JS) is a plus Independent and efficient, you can adapt to operational constraints Being multi-skilled, you know how to approach your project with a new look in order to imagine solutions that are concrete and focused on users You are passionate for design and people You will be directly involved in the exponential development of UX design in Altran You can work in a professional environment in English German is a plus You will be able to work side by side with the members of your team and the other centers of expertise during all stages of the projects by contributing to team dynamics You are willing to travel to France for trainings at Innovation and Design World Class Center Strong communication skills (written, verbal, presentation) are a big plus
Inserat ansehen

26.03.2020

Altran Switzerland AG

Automation Engineer

  • Altran Switzerland AG

  • 4051Basel

  • 26.03.2020

  • Vollzeitstelle

Job TitleAutomation Engineer Vacancy Reference Number22496 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Lead medium to large engineering projects from planning to assigning Development, testing and optimisation of automation production processes with DeltaV distributed control system Participation in risk analysis, operating tests and changeovers Responsible forcompliance with valid standards regarding security, hygiene, environment and quality Guarantee maximal plant availability Preparation and coordination of maintenance works with internal and external partners Continuous optimization of facilities, maintenance processes and internal works Processing and documentation of fault reports and implementation of maintenance plans Training of plant personnel with regards to processes and facilities Your profile Degree in Electrical Engineering, Automation Engineering or Computer Sciences Extensive knowledge of DeltaV distributed control system 5+ years of experience in GMP regulated biotech or pharmaceutical industry Fluent in German or English Flexible, structured and team player with good communication skills
Inserat ansehen

26.03.2020

Altran Switzerland AG

Machine Learning Engineer

  • Altran Switzerland AG

  • 4040Basel

  • 26.03.2020

  • Vollzeitstelle

Job TitleMachine Learning Engineer Vacancy Reference Number22500 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Design Machine Learning Systems and develop machine learning applications according to requirements Collaborate with product owners, data scientists and engineering teams to evaluate the effectiveness of the deployed ML systems Contribute in research, design, experimentation, development, deployment, monitoring and maintenance of ML model lifecycle Research and implement appropriate ML algorithms and tools Perform statistical analysis and fine-tuning using test results Process, clean, and verify the quality of data used for analysis Develop and implement best practices to enhance existing machine learning infrastructure Your profile Bachelor or Master Degree in IT, Computer Science, Mathematics or another related field 3+ years of relevant experience in machine learning or related role, preferably in the pharmaceutical or medical device industry Good knowledge of programming languages (eg. Python, R, Java, C++) Prior experience with SQL and NoSQL (e.g. document stores) databases Experience with cloud services Ability to clean and visualize data easily Understanding of Signal Processing Techniques and ability to solve problems Creative and critical thinking Fluent in English and/or German
Inserat ansehen

26.03.2020

Altran Switzerland AG

Data Scientist

  • Altran Switzerland AG

  • 4040Basel

  • 26.03.2020

  • Vollzeitstelle

Job TitleData Scientist Vacancy Reference Number22499 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Study and transform Data science prototypes Partner with the data platform and IT to ensure effectiveness of data strategy to resolve problems Select appropriate Datasets and Data Representation Methods Present and explain complex results or processes using clear and simple visualizations Apply statistical methods to tackle identified cases in an agile manner using multiple data sources and analytical tools Collaborate with other teams to develop appropriate solutions and to present business insights Your profile Master’s or Ph.D. in Data Science, Statistics, Mathematics, Computer Science or related field 3-7 years of experience building statistical models and manipulating data sets, preferably in pharmaceutical or medical device industry Experience working with all or some of the following technologies R, Python, SQL, Spark, Hadoop, Tensorflow, AWS, GitLab, GitHub, Shiny, Qlik, Tableau, Java Experience in statistical, data mining and machines learning techniques (like boosting, generalized linear models/regression, clustering, random forests, trees, and artificial neural network analysis etc.) Strong mathematical and analytical skills Excellent communication skills Fluent in German and/or English
Inserat ansehen

23.03.2020

Altran Switzerland AG

SW Installation Expert - DevOps

  • Altran Switzerland AG

  • 4051Basel

  • 23.03.2020

  • Vollzeitstelle

Job TitleSW Installation Expert - DevOps Vacancy Reference Number22425 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Software installation expert must install different equipment and maintaining them Focus on standardizing development environments and automating delivery processes to improve delivery predictability, efficiency, security and maintainability Support software developers with the installation of their lines of code in the software environment Provide developers more control of the production environment and a better understanding of the production infrastructure Execute the deployment of simple and complex IT systems Working on hardware and software networks and ensuring that the systems are functioning properly upon installation Being aware of safety and health regulations Your profile Bachelor's degree in computer science, electronics engineering or other engineering or technical discipline is required. Several years of experience in software installation projects Good IT skills with ONC, HND/HNC, NVQ, CSCS and C&G Ability to solve issues that arise on site
Inserat ansehen

22.03.2020

Altran Switzerland AG

System Engineer / Software Architect for Medical Devices

  • Altran Switzerland AG

  • 4051Basel

  • 22.03.2020

  • Vollzeitstelle

Job TitleSystem Engineer / Software Architect for Medical Devices Vacancy Reference Number21936 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting  A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D)  In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva Your role The ideal candidate will contribute to the development of software as medical device (SaMD) projects using stateof-the-art system engineering practices. Results-driven system engineer / cloud architect with a proven track record of innovative medical solutions. This highly interactive role will work with cross-functional teams and support various development activities including system conceptualization, system requirement definition, risk assessment, system verification and clinical validation. The primary responsibilities include: Design and implement system engineering approach to support the development and life cycle management of complex products and platforms in the areas of connected drug delivery devices, digital technologies, and SaMD  Involve in the creation and implementation of system engineering Standard Operating Procedures  SaMD Product & Project Management from Strategy to Development & Lifecycle Management in the regulated framework (ISO 13485, ISO 14971, IEC 62304, IEC 62366), incl. cross-functional/ stakeholders and supplier’s management  Io(Med)T and Digital Health Transformation incl. controlled/regulated ML/AI for Service-as-MD  Utilize the system engineering tool for requirement management and translate user and business needs into system/sub-system requirements  Author relevant design history files and GMP compliant documentations Your profile Technical Skills Software and System design using UML diagrams with good abstraction skills  Expertise in Web and Mobile application design, development and testing  Experience with Cloud and IoT architecture and technologies for complex systems  Knowledge of best practices for software development: Methodology (Agile and V-Model) and tooling (CI/CD, Automation, Requirement Management, etc.)  Experience with research, prototypes and PoC activities   Qualification Bachelor or more advanced degrees in Biomedical Engineering, Systems Engineering, Electrical Engineering, Computer Science, or other relevant disciplines  Prior experience covering the medical device or SaMD development from concept to commercial launch  Well-versed in medical device or SaMD development, Quality Management System, and regulatory processes (ISO 13485; IEC 60601, 62304, 82304)  Strong communication skills to both lead the technical discussions with vendors and also align with internal stakeholders to drive decisions
Inserat ansehen

20.03.2020

Altran Switzerland AG

Cell and Gene Therapy (Senior) Consultant

  • Altran Switzerland AG

  • 4051Basel

  • 20.03.2020

  • Vollzeitstelle

Job TitleCell and Gene Therapy (Senior) Consultant Vacancy Reference Number22413 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innvation and high-tech engineering consulting  A multi-stage model with carrer opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) In switzerland, Altran employs éore than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva      Your role Provide comprehensive scientific and technical strategic guidance in clinical and product development Assist in efficiency improvements (e.g.through novel microfluidic approaches) Support the client in working withcross-functionalteamsof molecular biologists, data scientists and bioprocess / automation engineers SupportGMP/GTPas well asregulatory compliance in the area of cell, gene and tissue therapies Workin alignment with internal as well asinternationalqualitystandards (ICH, ISO, etc.) Your profile PhD in molecular biology, cellular biology, stem cell biology, biomedical engineering or related fields within biological cellular systems 5+ years of relevant experience within the biotechnology/ pharmaceutical industry or clinical laboratories preferably with an oncology background Experience in cellular, tissue and gene therapies,working with mammalian cell cultures Technical skills in pre-clinical, clinical and commercial production for cell therapy biopharmaceuticals and proteins Knowledge of important quality systems, preferably in sterile production environments Excellent verbal and written communication skills as well as excellent time management and organizational skills Ability to generate new ideas, achieve results and solve problems Fluent inEnglish(German & French is an advantage) Further beneficial competencies include: Practical experience in the area of CAR-T-Cell Therapy,in vitro and in vivo cell differentiation systems Practical competencies in cell or gene therapy technologies (e.g. viral delivery systems, upstream & purification systems, bioprocessing) Workingknowledge of Supply Chain Managementas well ascommercialisation and reimbursement strategies for CGT Ability to writeregulatory submissions (pre-IND briefing packages, INDs, and BLAs/NDAs)and/orexperience withnational regulatory authorities Experience in technology transfer   If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful.   Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland.   Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities 
Inserat ansehen

20.03.2020

Altran Switzerland AG

(Senior) Project Manager in Engineering

  • Altran Switzerland AG

  • 4051Basel

  • 20.03.2020

  • Vollzeitstelle

Job Title(Senior) Project Manager in Engineering Vacancy Reference Number22412 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required10 years of experience and more Our offer A permanent contract with the leader in innvation and high-tech engineering consulting  A multi-stage model with carrer opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) In switzerland, Altran employs éore than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva  Your role Ensure that projects aredelvieredwith quality,on time andwithinbudget Monitor and update tasksand report on the status ofproject deliverables Manage global project teamsand ensure good communication within the teams Manage stakeholder expectationsbased on their involvement and impact on the project Organize and moderateinternal meetings& workshops(incl. preparation of meetingminutes) Coordinate& prepare steering committees to reviewproject milestones Ensureknowledge sharing between teams and advice on best practices andproject management principles Establishan effectiverisk management Your profile 10+ years of professional experience in LifeSciences, Healthcare, Biotech/Pharma, MedicalTechnology or related industries, preferably within a technical function B.Sc.and Masters degree(e.g.in Engineering,Business Administration, Health Sciences) Valid Project Management Certification (e.g.PMP, PRINCE2) Proven track record in leading technical projects in engineering or related fields of work Ability to leadcross-functionaland possibly internationalteams Ability to work with stakeholderson any level (C-Level, Directors, Department Heads, Project Team, etc.) Exceptional communication and presentation skills – both written and verbal Fluent in English; German at least B1/B2  Further beneficial competencies include: Applied knowledge in agile (project management) methodologies (e.g. Scrum, SAFe)     If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful.   Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland.   Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities.
Inserat ansehen

20.03.2020

Altran Switzerland AG

Manufacturing Engineer

  • Altran Switzerland AG

  • 4051Basel

  • 20.03.2020

  • Vollzeitstelle

Job TitleManufacturing Engineer Vacancy Reference Number22418 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva Your role This role supports manufacturing operations in the areas of process development, tool design, machine programming & layout, machinery & equipment, continuous improvement and other duties associated with engineering support of production. The ideal candidate will provide direction and technical support regarding: Equipment design and development Testing of materials Preparation of specifications and operator instructions Process studies, investigations and root cause analysis Responsibilities:   Analyse and establish current condition of processes, identify waste, develop future target state and implement lean processes and systems to improve efficiency to reduce overall lead time, while maintaining quality and security Formulate key performance indicator measurements during implementation, and simultaneously monitor progress and record data Develop manufacturing methods, labor utilization standards, and cost-analysis systems to promote efficient staff and facility utilization Coach and mentor a multi-skilled team with emphasis on quality, customer delivery performance & cost control Work adaptively and proactively to address potential performance/delivery issues and apply real-time problem-solving skills to obstacles and shortfalls. Apply Lean Manufacturing / Continuous Improvement (CI) tools Your profile Master Degree in Manufacturing Engineering, Industrial Engineering, Process Engineering, or other related Engineering degree 5-7 years of experience required in a pharmaceutical manufacturing environment Previous experience working in a regulated industry (cGMP, FDA guidelines, EU regulations, Swiss Medic) such as Medical Device is preferred. Demonstrated proficiency in Lean Management (Six Sigma Black Belt certification) Proven Managerial and leadership skills Excellent Analytical, problem-solving skills Languages: English mandatory, German is a big plus
Inserat ansehen

20.03.2020

Altran Switzerland AG

Medical Device Project Manager

  • Altran Switzerland AG

  • 4040Basel

  • 20.03.2020

  • Vollzeitstelle

Job TitleMedical Device Project Manager Vacancy Reference Number22410 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer Altran is the global leader in Innovation, Digital and High-tech engineering consulting. At Altran, you get the chance to work on projects among a multi disciplinal portfolio and you become part of our international community of like-minded experts! Our Life Sciences Division in Switzerland is providing Digital and Engineering services from the conception, through development, quality assurance and transfer to production, implementation, and rollout. We are proud to collaborate with the major players of the MedTech, Biotech and pharmaceutical sectors to strengthen their market share. Follow your passion in a role where you will be exposed to the technologies and processes that leading global companies utilize, and join our innovative team as, Medical Device Project Manager .   Your role Responsibilities : Participate in the analyses to understand product requirements, value propositions to customers and configuration build up. Define the prototyping, design, planning and roadmap of the project. Lead, plan and coordinate a multidisciplinary engineering team that will prototype and design the system according to the project roadmap. Create and maintain detailed project plans with work breakdown, deliverables, milestones, resources and responsibilities. Identify and engage with potential suppliers (technology, equipment). Provide timely and accurate information to management. Your profile Requirements:  MS Engineering / Science or equivalent. 8+ years of experience as a Project Manager on the development of a medical device combining Software and Hardware and integrating several imaging modalities including ultrasound. Experience in early stage prototype development. Experience in carrying out developments from the research phase to the market authorization phase. Knowledge of medical imaging and image processing. Ability to communicate effectively and build relationships with internal/external stakeholders. Leader without hierarchical power. Excellent organization and communication skills. Team player, pro-active, can-do attitude, active driver. Strong communicator with good influencing skills.   If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful. Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland.   Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities.   Our Offer   A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva.
Inserat ansehen

19.03.2020

Altran Switzerland AG

Regulatory Affairs Specialist

  • Altran Switzerland AG

  • 4051Basel

  • 19.03.2020

  • Vollzeitstelle

Job TitleRegulatory Affairs Specialist Vacancy Reference Number22400 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Support preparation of technical documentation or design dossier documentation for submission to and review by Notified Bodies, as required (both MDD and MDR) as assigned Provide regulatory support for Life Cycle Management projects as assigned Manage data cleansing and comparison, remediation and maintenance of existing Technical File documentation as instructed and assigned. Perform Regulatory reviews for Labeling and Promotional Material of CE marked devices Perform Regulatory Change assessments as assigned Support compliance execution work in collaboration with local Regulatory Team. Your profile At least 5 years of experience in Medical Device Industry and Regulatory Affairs. Understanding of MDR requirements regarding required content of Technical Documentation (focus on ANNEX II of Regulation (EU) 2017/745) Understanding of requirements of current Council Directive 93/42/EEC Previous experience within Regulatory Affairs is preferred Experience with creation and maintenance of Technical Documentation in PLM Systems preferred Experience in IT system documentation and database management preferred   Ability to comprehend principles of engineering, physiology and medical device use. Strong analytical skills and proficiency in English written and spoken. German in addition, would be an asset. 
Inserat ansehen

13.03.2020

Altran Switzerland AG

Senior Design Quality Engineer

  • Altran Switzerland AG

  • 4051Basel

  • 13.03.2020

  • Vollzeitstelle

Job TitleSenior Design Quality Engineer Vacancy Reference Number20920 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Drive continuous improvement of Design Control and Risk Management processes  Work analytically using statistical methods and process/design excellence tools to establish test plans as well as evaluate test data  Coordinate and conduct design verification and validation activities as well as design / process failure mode effects Act as a leader in all areas of the Quality System, including, but not limited to Corrective & Preventive Actions, Complaints, Nonconforming Materials, Risk Management, etc.  Accountable for the successful delivery of multiple simultaneous projects, spanning multiple functional areas and locations Identify, monitor and manage potential project risks by creating a risk plan Responsible for clear project scope definition and deliverables, milestones, timeline  Work closely with various stakeholders and be an active role in the Design Control team.  Your profile A minimum of a Bachelor’s degree in Engineering or related technical or scientific discipline with a minimum of 7+ years of experience in related field is required  Working knowledge of Design Controls, GMPs, QSR, 21 CFR 820, MDD 93/42/EEC, ISO13485 and ISO14971 quality requirements is required Previous Quality Engineering experience is preferred Experience in an Medical Device regulated environment Fluency in English and German is a strong asset
Inserat ansehen

13.03.2020

Altran Switzerland AG

Quality Expert for Medical Devices

  • Altran Switzerland AG

  • 4040Basel

  • 13.03.2020

  • Vollzeitstelle

Job TitleQuality Expert for Medical Devices Vacancy Reference Number21708 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Write, Review and approve deliverables (e.g. procedures, records, third party work, contractors, clinical trial material, components) and related tools (e.g. IT, document systems, training tools, facility validation) to ensure GMP compliance. Accountable for monitoring, analysis and reporting of GMP related KPIs as part of management reporting. Manage quality problems and technical matters and ensure they are resolved consistently and in accordance with global standards and policies. Release of medical devices for clinical studies and commercial use. Support Medical Device Risk Management, through proactive risk management tools and approaches, to minimize impact on global supplies and patients. Perform or support inspections and audits as required.   Meet internal and external guidelines regarding quality and safety (quality manuals, regulatory cGMP guidelines, health authority requirements, SOPs, HSE, etc.). Promote and enforce compliance to guidelines. If managing associates, ensure same for them. Your profile Graduate in Chemistry, Pharmacy, Microbiology or Biotechnology or another related science. At least 3 years of relevant experience. Ability to influence people, negotiate and communicate. English fluent in speaking / writing, German and/or French desirable.  Sound scientific, technical and regulatory knowledge in a specific area. Excellent knowledge of cGMP, working knowledge of medical device and combination, product regulations, standards and guidelines. Good knowledge of medical device development and life-cycle management.  Good organizational skills.  Good and proven ability to analyse and evaluate GMP compliance.
Inserat ansehen

12.03.2020

Altran Switzerland AG

Solution Architect - Cloud Platform for eHealth Data

  • Altran Switzerland AG

  • 4040Basel

  • 12.03.2020

  • Vollzeitstelle

Job TitleSolution Architect - Cloud Platform for eHealth Data Vacancy Reference Number22320 Work SiteSwitzerland / | CHE - All Regions / Basel Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer Altran is the global leader in Innovation, Digital and High-tech engineering consulting. At Altran, you get the chance to work on projects among a multi disciplinal portfolio and you become part of our international community of like-minded experts!   Our Life Sciences Division in Switzerland is providing Digital and Engineering services from the conception, through development, quality assurance and transfer to production, implementation, and rollout.   We are proud to collaborate with the major players of the MedTech, Biotech and Pharmaceutical sectors to strengthen their market share. Follow your passion in a role where you will be exposed to the technologies and processes that leading global companies utilize, and join our innovative team as   Solution Architect - Cloud Platform for eHealth Data.   If you have a real passion for designing and delivering well-architected solutions that will unlock the value of data across science, then this is the opportunity you have been waiting for:   Your role Design solutions that will form foundational data platforms, aligned to our clients’s data science and AI strategies. Provide the architectural leadership to craft requirements and opportunities into well-architected solutions across cloud and on-premise infrastructure. Responsible for ensuring that the solutions you help deliver form an integral part of our client’s estate and align with the architecture and domain roadmaps. Support the architecture direction and solution delivery for data ingestion and storage to improve reuse, ensuring optimal dataflow and processes both on premise and in the cloud. Work with external partners in the delivery of reciprocal solutions that support standard methodology data management whilst ensuring architectural standards are maintained. Delivery of the platform components to enable a robust data architecture. Your profile A deep understanding of the Pharmaceutical Industry and Digital Therapeutics. Knowledge of technical solutions and associated data utilized in drug discovery and patient treatment. Experience with a range of infrastructures and technology stacks needed to support global solutions. Knowledge of designing/developing innovative solutions, blueprints, and standards for solution design. Hands-on experience with cloud technologies (AWS, Azure, GCP). Practical experience in agile delivery of complex IT projects. Understanding of current and new technologies and their applicability to the Science domain. Knowledge of the high-level business processes/workflows and associated dataflow. Excellent communication skills and fluency in English.   If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful.   Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland.   Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities.   Our Offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva.
Inserat ansehen

29.03.2020

Altran Switzerland AG

CAPEX Project Manager - Pharma

  • Altran Switzerland AG

  • 3002Bern

  • 29.03.2020

  • Vollzeitstelle

Job TitleCAPEX Project Manager - Pharma Vacancy Reference Number20915 Work SiteSwitzerland / | CHE - All Regions / Bern Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Manage capital projects from basic design to execution and qualification/validation and deliver on time, within budget and according to defined specifications Ensure the required quality, regulations and guidelines compliance Build, coordinate and manage the project teams, cross functional, local or regional Manage all project -related documentation such as qualification (“DQ, IQ, OQ, PQ”) and requirement specifications Perform project controls for cost and schedule according to engineering standards: Measure progress, forecast cost spend and initiate preventative and corrective actions if needed. Your profile BSc/MSc degree in Process/Biotechnology/Mechanical Engineering or equivalent Project management certified At least 5 years' experience in process engineering or equivalent and capital project management  with high complexity in the chemical, biotech- or pharmaceutical industry   SAP-, DMS- and COMOS-system experience preferred  Relevant quality standards knowlegde as well as local safety policies and guidelines German and English fluent               
Inserat ansehen

27.03.2020

Altran Switzerland AG

Commissioning Qualification and Validation (CQV) Engineer

  • Altran Switzerland AG

  • 3002Bern

  • 27.03.2020

  • Vollzeitstelle

Job TitleCommissioning Qualification and Validation (CQV) Engineer Vacancy Reference Number22013 Work SiteSwitzerland / | CHE - All Regions / Bern Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting. A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Support of continuous improvement on process, and on Qualification and Validation projects. Generate and execute CQV protocols using Good Documentation Practices (GDPs). Investigate and resolve protocol exceptions or discrepancies. Develop technical reports and CQV summary reports. Collaboration in the creation of user requirements (URS). Create / check DQ, IQ, OQ and PQ documents. Participation in GMP relevance and risk analyses. Develop Standard Operating Procedures (SOPs), process workflows, Validation Master Plans, User Requirement Specifications, Turnover Packages, and other regulatory support documentation (CAPA etc). Your profile BSc/MSc degree in Engineering or Chemistry or any related field. Minimum 3 years of experience in Commissioning and/or Qualification and/or Validation in the Pharmaceutical industry. Applied knowledge of international Pharmaceutical regulations is preferred. Applied Knowledge of creation and verification of qualification equipment plans (FAT/SAT/DQ/IQ/OQ/PQ). Fluent in English and German. If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful. Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland. Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities.
Inserat ansehen

27.03.2020

Altran Switzerland AG

Ingénieur Electrique - Production

  • Altran Switzerland AG

  • 3002Bern

  • 27.03.2020

  • Vollzeitstelle

Job TitleIngénieur Electrique - Production Vacancy Reference Number22003 Work SiteSwitzerland / | CHE - All Regions / Bern Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer Afin de renforcer nos équipes en Suisse Romande, nous sommes à la recherche d’un ingénieur électrique afin de travailler dans un environnement de production industriel.   Your role Activités - Réaliser l’étude électrique nécessaire à l’implantation de composants électrotechniques de type informatique Industrielle dans nos équipements de production - Prendre contact et valider les modifications envisagées auprès des fabricants et/ou fournisseurs des équipements visés - Assurer l’installation et les tests de fonctionnement en coordination avec nos services de production et informatique - Mettre à jour, ou assurer le suivi de la mise à jour de la documentation machine dans le respect des standards de l'entreprise - Rédiger un rapport d’intervention détaillé à l’issu de la modification et des tests effectué - Réaliser les études de modifications électriques nécessaires à l’implantation de composants électrotechniques de type Informatique Industrielle dans nos équipements de production (à des fins de sécurisation) - Se coordonner avec l’équipe en charge de l’étude informatique de ces connexions - Suivre l’installation et les tests de fonctionnement en coordination avec nos services méthodes et gestion Maintenance, production et informatique.   Your profile Profil - Ingénieur HES ou équivalent avec expérience dans le domaine industriel - Solide connaissances et expériences en architecture de contrôle commande PC et automate sur machine de production, notamment sur machines spéciales - Connaissances et expériences en dimensionnement de composants électrotechniques en environnement industriel - Connaissances dans le câblage d’armoire électrique sous critères de certification CE - Esprit méthodique et organisé permettant un suivi qualitatif et quantitatif d’une intervention complète depuis la réalisation jusqu’au tests et capitalisation - Culture souhaitée de la gestion du délai, de l’anticipation et de l’analyse de risque Langues : Français et Anglais. Ce poste vous intéresse alors rejoignez-nous ! Nous restons très volontiers à votre disposition pour tout complément d'information.  
Inserat ansehen

11.03.2020

Altran Switzerland AG

Process Engineer

  • Altran Switzerland AG

  • 3002Bern

  • 11.03.2020

  • Vollzeitstelle

Job TitleProcess Engineer Vacancy Reference Number22296 Work SiteSwitzerland / | CHE - All Regions / Bern Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer   For our current customer project in the Bern region, we are looking for a qualified and experienced engineer with LabView.   Our Mission As a consultant, you advise and assist our customers with their technology challenges. Throughout your career, you can work on different project phases from technical and strategic studies, design and development of new products, their introduction into the production over launch of comprehensive services and solutions. Helping clients to realize ideas from ideation, prototyping, industrialization of products, manufacturing, scale-up, distribution as well as service provisioning/support.   Your role   We are looking for a Process Engineer with extensive LabView experience Find solutions to support the production process within supply chain. Interact with different departments (e.g. quality and customer complaints) Maintenance of existing code lines, bug fixing and upgrades including documentation   Your profile Completed MSc Degree in Engineering Expert Level in LabView 3-5 years of industry experience ideally in a process engineering position Good knowledge of production oriented processes Team player with open mindset Fluent in English, French or German is a plus   Altran Benefits A multi-stage model with career opportunities through specialization prospects, as well as through continuing professional education and training. A steep learning curve due to diverse and cross-industrial opportunities. Develop additional skills in project or quality management as well as requirements engineering. Team-oriented working atmosphere with regular community events. A multinational culture with over 50,000 colleagues in over 30 countries. Global projects & global job opportunities.   We are looking forward to receiving your detailed application including motivational statement and diploma copies . We only accept applications through our online career portal. Applications via e-mail or 3rd party platforms will be deleted due to GDPR regulation. You can track your application statushere. Your application may be considered for other open positions. Altran only accepts direct applications (no recruitment agencies). For more information contact directly our Talent Acquisition Manager,Pascale Nathalie Käch.    
Inserat ansehen

08.04.2020

Altran Switzerland AG

CQV Project Manager

  • Altran Switzerland AG

  • 8005CH 8005 Zürich

  • 08.04.2020

  • Vollzeitstelle

Job TitleCQV Project Manager Vacancy Reference Number16752 Work SiteSwitzerland / | CHE - All Regions / All Regions Contract TypePermanent [Full-Time] Minimum number of years of experience required10 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role   Ensure that Commissioning and or Qualification projects are planned managed to meet company standards by following the approved standards Ensure the CQ PM understands the new approach to Commissioning (C) and/or Qualification, is followed and become SME in the approach. Work with Global Engineering PMs in Switzerland to plan, estimate, manage and deliver CQ projects within budget. Ensure the CQ PM is involved in the preliminary planning understand the needed inputs to commissioning and develop and share them in a timely basis. Manage the CQ documents developed by engineering and consultants as part of projects and personnel in a dynamic environment. Your profile   Bachelors degree in Process-, Chemical-, Mechanical- or Bio Engineering and/or equivalent knowledge 10+ year experiences in Commissioning and Qualification in the area pharma and biopharma In depth knowledge with E2500 and or other Risk Based Approaches on Commissioning Qualification projects We are looking for a Subject Matter Expert in FAT (SAT) planning and execution Hands on experiences in black and clean utilities, APIs, mAb (both stainless steel and Single Use), fill/finish Fluency in English and German Demonstrates strong leadership -, communication -, and interpersonal skills
Inserat ansehen

04.04.2020

Altran Switzerland AG

Human Factors Engineer

  • Altran Switzerland AG

  • 8012Zürich

  • 04.04.2020

  • Vollzeitstelle

Job TitleHuman Factors Engineer Vacancy Reference Number22108 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva Your role To support the development of the medical device team we are seeking a human factors engineer to lead all related activities in developing medical devices/combination product and apps from early phase to late phase development. This position is part of multidisciplinary and international teams, spanning across multiple projects, with human factors engineering being a key element for success.   Responsabilities : The Human Factors Engineer will provide expert input to the device development teams to establish system, design, operating requirements, support design of packaging, labelling and user interface The candidate will be responsible for independently leading, planning, executing and reporting of human factors studies with users to evaluate the user interface design and propose improvement Tasks: Roll out the Human Factors strategy by planning the activities accordingly and performing/documenting the planned activities (e.g. user studies, design input) Strong communication and negotiation skills are key to influence diverse stakeholders Provides human factors support throughout the product development lifecycle including user needs identification, development of user profiles and use scenarios, task analysis, use-related risk analysis, generation of hardware and software design concepts, generation of instruction for use (creation graphical user interfaces, and product graphics), user interface design and instructions for use Plans and executes formative and summative user studies, reporting and presenting design recommendations to the project team either using external vendors or using internal facilities Design Instruction for Use and User Interface Performs anthropometric, biomechanical, ergonomic, and systems safety analyses to identify and assess risk in product development Propose design optimization of the developed product Your profile Bachelor’s or Master degree in engineering, ergonomics, psychology, human factors, usability, user interface design, industrial design/graphic design or related discipline Excellent skills in English, verbal and written are required An ideal candidate would have a relevant degree and 5 to 10 years of experience in applying Human Factors Engineering/usability to medical devices development, preferably in the pharmaceutical industry, including: Good understanding and specific knowledge on applying Human Factors Engineering processes to medical device development from concept generation to health authority submission Experience in project / program management Experience in developing apps, software and/or industrial design Experience in managing user studies (performed by vendors or self-managed) Experience in developing and documenting Human Factors activities for medical devices as required by regulation Good understanding of the risk management activities
Inserat ansehen

03.04.2020

Altran Switzerland AG

Electrical Engineer Power Converter

  • Altran Switzerland AG

  • 8058Zürich

  • 03.04.2020

  • Vollzeitstelle

Job TitleElectrical Engineer Power Converter Vacancy Reference Number19946 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypeUnbefristet [Vollzeit] Minimum number of years of experience required5 years of experience and more Our offer Wir suchen per sofort oder nach Vereinbarung motivierte Elektro-Ingenieure mit Erfahrung in der SW-Entwicklung um unser erfolgreiches Team beim Kundenprojekt zu erweitern. Als Ingenieurdienstleister begleiten wir bereits seit 30 Jahren Kunden bei der Einführung neuer Lösungen und Konzepte.  Damit bieten wir unseren Consultants ein vielseitiges Portfolio an Projekten und Kunden. Sind Sie bereit für eine neue technische Herausforderung? Your role Mit unserem Kompetenzteam zusammen entwickeln Sie neue Antriebsstromrichter-Technologien Im Bereich Traction Control übernehmen Sie die Spezifikation, Implementierung sowie Dokumentation von Software für Stromrichter Sie entwickeln innovative Lösungen für ein neues Software-Design mittels Matlab, Simulink sowie Codesys inkl. Simulation Nach erfolgreicher Simulation übernehmen Sie die Implementierung vor Ort (Reisebereitschaft ca. 5-10% in Europa) Your profile Abgeschl. MSc. Studium in der Elektrotechnik Mind. 3-5 Jahre praktische Industrie-Erfahrung in der Prozesssteuerung und Software-Design (Matlab, Simulink, Codesys) Fachwissen im Bereich Steuerungs- sowie Regelungstechnik (Power Electronics) Erfahrung mit elektrischer Ausrüstung in der Bahnindustrie Fliessende Deutsch- sowie Englischkenntnisse in Wort und Schrift Erfahrung in der Inbetriebnahme komplexer Lösungen vor Ort (Reisebereitschaft)     We are looking forward to receiving your detailed application including motivational statement and diploma copies . We only accept applications through our online career portal. Applications via e-mail or 3rd party platforms will be deleted due to GDPR regulation. You can track your application statushere. Your application may be considered for other open positions. Altran only accepts direct applications (no recruitment agencies). For more information contact directly our Talent Acquisition Manager,Mark Swerissen.
Inserat ansehen

03.04.2020

Altran Switzerland AG

Business Development Manager Industry

  • Altran Switzerland AG

  • 8057Zürich

  • 03.04.2020

  • Vollzeitstelle

Job TitleBusiness Development Manager Industry Vacancy Reference Number21413 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypeUnbefristet [Vollzeit] Minimum number of years of experience required10 years of experience and more Our offer Für unser Team im Bereich Industrie, Aerospace und Bahntechnik in Zürich suchen wir eine(n) erfahrene(n) Business Development Manager/In (5-10 Jahre praktische Berufserfahrung), der/die laufende Verkaufsaktivitäten sowie künftige Erschliessung neuer Kunden in der Deutschschweiz weiter entwickelt. Your role Aktive Mitarbeit im Verkauf der Altran Global Industry Dienstleistungen Umsetzung der Gruppenstrategie für den Markt Deutschschweiz (Zürich, Bern, St. Gallen, Basel, Zentralschweiz) Entwicklung neuer strategische Verkaufskampagnen sowie neuer Absatzmärkte Abwicklung von komplexen Projektangeboten in der Verkaufsphase Strukturierung der Dienstleistungen sowie Koordination mit den operationellen Abteilungen Netzwerken sowie Lobbying auf C-Level mit bestehenden sowie neuen Kunden Regionenübergreifende Zusammenarbeit in der Angebotsphase Your profile Abgeschlossenes Masterstudium in Betriebswirtschaft kombiniert mit einem Background in der IT oder Elektrotechnik 5 bis 10 Jahre solide praktische Berufserfahrung im Verkauf von technischen Dienstleistungen in der Schweiz Ausgezeichnetes bestehendes Netzwerk in der schweizerischen Industriebranche (Consulting Erfahrung von Vorteil) Deutsche Muttersprache (inkl. schweizerdeutsch) und fliessende Englischkenntnisse, weitere Fremdsprachen von Vorteil Teamplayer mit guter methodischer und selbständiger Arbeitsweise Nachweisbarer Führungserfahrung sowie ausgezeichnete Kommunikationsfähigkeiten   Wir freuen wir uns auf Ihre vollständigen Bewerbungsunterlagen (Motivationsschreiben, CV, Arbeitszeugnisse sowie Diplome) ausschliesslich über die Career Page. Bitte beachten Sie, dass aus GDPR Gründen Bewerbungen per E-Mail, Post oder Drittplattformen gelöscht werden. Sie können hierjederzeit Ihren aktuellen Bewerbungsstatus nachverfolgen und unsere aktuellen offenen Stellen prüfen. Ihre Bewerbung könnte auch für andere Positionen geprüft werden. Bei Fragen wenden Sie sich direkt an: Mark Swerissen, Talent Acquisition Manager. Altran akzeptiert ausschliesslich Direktbewerbungen.
Inserat ansehen

01.04.2020

Altran Switzerland AG

Software Developer - Life Science

  • Altran Switzerland AG

  • 8044Zürich

  • 01.04.2020

  • Vollzeitstelle

Job TitleSoftware Developer – Life Science Vacancy Reference Number15002 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer Altran is the global leader in Innovation, Digital and High-tech engineering consulting. At Altran, you get the chance to work on projects among a multi disciplinal portfolio and you become part of our international community of like-minded experts!  Our Life Sciences Division in Switzerland is providing Digital and Engineering services from the conception, through development, quality assurance and transfer to production, implementation, and rollout.  We are proud to collaborate with the major players of the MedTech, Biotech and Pharmaceutical sectors to strengthen their market share. Follow your passion in a role where you will be exposed to the technologies and processes that leading global companies utilize, and join our innovative team as Software Developer – Life Science. Your role Participate in all phases of software development from feasibility studies through design, development, testing and bug fixing including software maintenance. Participate in defining work packages, their estimation, planning, and implementation within the development team. Produce based on software requirements, the project’s software architecture and other project guidelines: accurate code design and implementation including the tests to verify the code against specification. Provide all necessary documentation according to the software development process. Review and analyze your source code as well as on request the source code of your peers in the development team;Review application design, functionality, usability and performance to enhance it.  Provide work status and issue notification within the test automation team. Executing test cases during preliminary & final test phases, analyzing test results, reporting and tracking issues, and verifying fixes.  Build software that tests software either by coding or by integrating third party tools into our test suites. Your profile BS/BA degree in computer science, science or engineering. Minimum of 3 years directly related experience in Testing on different levels (unit / component / integration / end to end / UI). Programming in C, C++, C#, .net, Python in the scope of test automation.  Build management Design patterns. Expert knowledge of engineering principle and concepts.  Develops and uses company design practices as applied to projects. Understands and applies industry practices and benchmarks.  Uses company practices for SW integration and test at the expert level. German and English proficient level as ideal or just Advanced English. If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful. Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland.   Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities. Our Offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva.
Inserat ansehen

30.03.2020

Altran Switzerland AG

Embedded Test Engineer Labview

  • Altran Switzerland AG

  • 8057Zürich

  • 30.03.2020

  • Vollzeitstelle

Job TitleEmbedded Test Engineer Labview Vacancy Reference Number22522 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypeUnbefristet [Vollzeit] Minimum number of years of experience required5 years of experience and more Our offer Für unser aktuelles Kundenprojekt vor Ort (im Zürcher Oberland) suchen wir dringend einen Test Ingenieur mit Embedded Erfahrung. Diese spannende Aufgabe beinhaltet viele Einflussgrössen und erfordert eine systematische und neugierige Arbeitsweise. Your role Auslegung und Inbetriebnahme neuer Prüfstände (Mechanik, Eletrkonik und Automation) Erstellung neuer System-Anforderungs- und Integrationstest-Spezifikationen anhand der Systemanforderung und -Architektur Auswertungen von Bugs und Testberichten inkl. Reporting an Test Manager Erarbeitung Visual Test Shells mittels Python sowie Softwareentwicklung (C++) Neuentwicklung von Unit Testing gemäss Konzept Analyse verschiedener Betriebszustände sowie das generelle Systemverhalten und -stabilität Dokumentation der Testkonzepte sowie deren Ergebnisse   Your profile Abgeschl. Studium mit Fokus Elektr. Ing. und/oder Informatik Mind. 3-5 Jahre Erfahrung im System Testing sowie -Entwicklung mit C++ und/oder Embedded SW Erfahrung in der LabView Programmierung Gewandt im Umgang mit Messmitte ISTQB zertifiziert Kenntnisse mit JIRA/Confluence SPS Programmierung (z.B. Beckhoff) ist von Vorteil Fliessende Deutschkenntnisse (W/S)   Wir freuen wir uns auf Ihre vollständigen Bewerbungsunterlagen (Motivationsschreiben, CV, Arbeitszeugnisse sowie Diplome) ausschliesslich über die Career Page. Bitte beachten Sie, dass aus GDPR Gründen Bewerbungen per E-Mail, Post oder Drittplattformen gelöscht werden. Sie können hierjederzeit Ihren aktuellen Bewerbungsstatus nachverfolgen und unsere aktuellen offenen Stellen prüfen. Ihre Bewerbung könnte auch für andere Positionen geprüft werden. Bei Fragen wenden Sie sich direkt an: Mark Swerissen, Talent Acquisition Manager. Altran akzeptiert ausschliesslich Direktbewerbungen.  
Inserat ansehen

30.03.2020

Altran Switzerland AG

Qualification Engineer

  • Altran Switzerland AG

  • 8058Zürich

  • 30.03.2020

  • Vollzeitstelle

Job TitleQualification Engineer Vacancy Reference Number22082 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer Altran is the global leader in Innovation, Digital and High-tech engineering consulting. At Altran, you get the chance to work on projects among a multi disciplinal portfolio and you become part of our international community of like-minded experts! Our Life Sciences Division in Switzerland is providing Digital and Engineering services from the conception, through development, quality assurance and transfer to production, implementation, and rollout. We are proud to collaborate with the major players of the MedTech, Biotech and pharmaceutical sectors to strengthen their market share. Follow your passion in a role where you will be exposed to the technologies and processes that leading global companies utilize, and join our innovative team as a  Qualification Engineer. Your role Support of continuous improvement on processes, and on Qualification and Validation projects Conduct diverse qualification activities (FATSAT, IQ, OQ, PQ) on manufacturing products for clinical phases Support the team with the implementation of a new filling line Plant optimization, troubleshooting and implement new process equipment Review of technical documentation Supporting the team on various projects Your profile A minimum of a Bachelor’s degree in Engineering or related technical or scientific discipline Working experience in pharma and in quality, ideally with filled-finished products Good communicator and detailed-oriented mindset Fluent in English and German If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful. Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland. Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities. Our Offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva.
Inserat ansehen

29.03.2020

Altran Switzerland AG

Process Engineer Pharma

  • Altran Switzerland AG

  • 8058Zürich

  • 29.03.2020

  • Vollzeitstelle

Job TitleProcess Engineer Pharma Vacancy Reference Number16822 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva Your role Assess existing processes and equipment and identify and implement improvements. Implement new or transferred manufacturing processes in a timely manner. Lead and/or participate in equipment and process validations, assist in troubleshooting of process and/or equipment issues. Automation & Factory Support specifics: Assist in designing and implementing new equipment and tools to improve manufacturing efficiencies, reduce ergonomic stress, and improve quality. Create and update drawings using Pro/Engineer or SolidWorks. Work as part of a project team in the development and/or implementation of new equipment and tools. Technical support for daily production issues related to manufacturing equipment. Assist in addressing, owning, and resolving quality related issues for the manufacturing departments (ex CAPAs, and Audits) Your profile Master degree in a directly related discipline (Engineering, Biology, etc). Minimum 5 years of related experience Knowledge,  Automation & Factory Support specifics: Experience with automated manufacturing equipment and automation technologies.  Experience with Lean Systems. Quality Support specifics: Experience in reagent or instrument manufacturing for a Medical Device or Pharmaceutical company. Experience in a regulated environment. Knowledge of FDA Quality System Regulations (QSRs). Languages: English fluent, German is a plus
Inserat ansehen

28.03.2020

Altran Switzerland AG

Product Assurance Engineer Aerospace

  • Altran Switzerland AG

  • 8058Zürich

  • 28.03.2020

  • Vollzeitstelle

Job TitleProduct Assurance Engineer Aerospace Vacancy Reference Number22034 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer To strengthen our on premise team in Zurich we are looking for Product Assurance Engineer Consultant. As a PA Engineer consultant you will provide the necessary expertise and assistance to further improve and maintain the quality standards for their operations and products of our client. Your role Ensure hardware and software quality, product reliability, electronic components, standards, materials, mechanical parts, critical industrial fabrication processes and configuration control Initiating improvements to the quality management system, ensuring compliance to all relevant quality standards and regulatory requirements Implementation of PA requirements in accordance with customer standards Plan, conduct and monitor testing and inspection of materials and products to ensure finished product quality Monitoring the product in different phases (design, manufacturing, assembly, transport and shipment) Ensure that all safety associated risk are adequately identified, assessed, minimized, controlled through the implementation of a safety assurance program Processing the product assurance and safety documentation in accordance with the requirements and standards of the customer Your profile MSc. Degree in Engineering and/or Physics 2 to 5 years of practical industry experience (as a consultant is a plus) Minimum 3 years of experience in Product Assurance and a minimum 5 years of experience in Quality Assurance experience in space manufacturing quality or similar is a must Certification in ISO 9100 or at least ISO 9001 Knowledge of aerospace standards Microsoft office ( Excel, word, power point, visio) Knowledge of SAP is considered a plus Fluent in English, German and French are a plus   We are looking forward to receiving your detailed application including motivational statement and diploma copies . We only accept applications through our online career portal. Applications via e-mail or 3rd party platforms will be deleted due to GDPR regulation. You can track your application status here. Your application may be considered for other open positions. Altran only accepts direct applications (no recruitment agencies). For more information contact directly our Talent Acquisition Manager, Mark Swerissen.
Inserat ansehen

20.03.2020

Altran Switzerland AG

Business Analyst - Pharma

  • Altran Switzerland AG

  • 8012Zürich

  • 20.03.2020

  • Vollzeitstelle

Job TitleBusiness Analyst - Pharma Vacancy Reference Number22409 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva Your role Be involved in the development of processes, procedures, workflows and other supporting documentation Provide S&OP, coordinate implementation of systems and processes Proactively drive approaches to maximize the use of data sources and transform data Collect user feedback and translate them into further stories Review and monitor regularly the risk log Develop & coordinate best practices and shared approaches Your profile At least 3+ year experience in an equivalent position, in a regulated industry (pharma/ biotech prefered) Excellent communicator, good at writing and presenting data Perfect understanding of Quality Systems, GxP and Pharma Industry in general Good understanding of new technologies (AI, predictive analytics, etc…)
Inserat ansehen

20.03.2020

Altran Switzerland AG

Regulatory Affairs Specialist

  • Altran Switzerland AG

  • 8012Zürich

  • 20.03.2020

  • Vollzeitstelle

Job TitleRegulatory Affairs Specialist Vacancy Reference Number22414 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 50'000 consultants around the world and revenue of EUR. 3.3 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) In Switzerland, Altran employs more than 300 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva Your role Develop, implement, communicate, and maintain global regulatory strategies and plans for devices Identify and communicate relevant guidance, policies, standards, and regulations Ensuring that the company's products comply with the regulations of government agencies Preparing and coordinating documentation Perform Regulatory reviews for Labeling and Promotional Material of CE marked devices Your profile Master’s degree in Regulatory Affairs, Life Sciences, or Engineering At least 5 years of experience in European Medical Device industry especially with regulatory, quality or engineering Understanding of MDR requirements regarding required content of Technical Strong knowledge of ISO 13485 and ISO 9001, QSR and Medical Devices applicable requirements, especially Council Directive 93/42/EEC and Regulation 2017/745, as they pertain to technical documentation Ability to comprehend principles of engineering, physiology and medical device use Strong analytical skills and proficiency in English written and spoken. German in addition, would be an asset
Inserat ansehen

16.03.2020

Altran Switzerland AG

Stress Engineer Aviation

  • Altran Switzerland AG

  • 8012Zürich

  • 16.03.2020

  • Vollzeitstelle

Job TitleStress Engineer Aviation Vacancy Reference Number19415 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required10 years of experience and more Our offer We are looking to increase our aviation engineering team in central Switzerland with an additional stress engineer who will be required to meet the technical specification, customer requirements and airworthiness regulations. This is a long-term project which requires us to continously building up teams, so we are looking to fill several open positions. Your role Conduct and lead structural analysis of aircraft structures (incl. fatigue calculations and spectrum generation), and work in a team environment collaborating with other engineers Perform fatigue safe-life and damage tolerance analyses to establish metallic component retirement times and inspection intervals Verify and check structural integrity by using appropriate analytical methods, finite element models/simulations and other analysis tools Support in-service products by investigating failures and analyzing improvements Conduct static design of components Conduct CAD conversion into practical calculation models Define and document technical substantiate reports for customer Check structural analysis reports Your profile MSc. in Mechanical Engineering and/or Aerospace with 4-7 years of aviation industry experience Strong knowledge of structural and stress analysis within the aerospace industry Experience with static structural analysis of metallic and/or composite structures using classical (hand calculation) and computer-based methods such as Finite Element Analysis (FEA) Experience with fatigue and damage tolerance analysis, especially for airborne applications Strong background utilizing classical hand analysis as well as finite element methods and tools. Strong and innovative problem solving skills Experience in coordinating with different teams and lead technical tasks Experience with AFGROW, or other similar DT tools Experience with Hyperworks/Femap, or other similar Finite Element Modeling (FEM) packages Fluent in English, B1 level in German Eligable to work in Switzerland and ITAR compliant    We are looking forward to receiving your detailed application including motivational statement and diploma copies . We only accept applications through our online career portal. Applications via e-mail or 3rd party platforms will be deleted due to GDPR regulation. You can track your application statushere. Your application may be considered for other open positions. Altran only accepts direct applications (no recruitment agencies). For more information contact directly our Talent Acquisition Manager, Mark Swerissen:mark.swerissen@altran.com.
Inserat ansehen

15.03.2020

Altran Switzerland AG

Electrical Engineer Controls

  • Altran Switzerland AG

  • 8057Zürich

  • 15.03.2020

  • Vollzeitstelle

Job TitleElectrical Engineer Controls Vacancy Reference Number21803 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required5 years of experience and more Our offer We are looking for a passionate and talenteda Electrical Engineer to join one of our on-premises project focusing on industrial control system design, integration, and release to manufacturing. The ideal candidate provides experience in industrial controls including power distribution, I/O, functional safety architectures, and the ability to own a component or sub-system from concept to manufacturing. Your role Work with an interdisciplinary team to execute product designs from concept to production including design, prototyping, validation, testing and certification Design and implement complex industrial control systems, test and validate those systems, and supporting field deployment of the systems Writing and developing functional specifications, design verification plans, and test procedures Working with external vendors to coordinate project deliverables to specifications Supporting product releases to manufacturing and customer deployments Establish development processes to meet industry standards for functionally safe control systems   Your profile MSc. in Electrical Engineering (or similar field) 5 - 8 years of experience in electrical and system level design Hands-on experience developing in industrial control systems Experience in electrical schematic design, and design for manufacturability Experience executing design reviews in front of interdisciplinary teams Extensive system design interfacing to a wide array of electro-mechanical subsystems Commitment to rigorous testing practices and design process flows Ability to resolve complex issues in creative, efficient, and effective ways   Any of the following would be a plus: Experience in developing industrial controls solutions including schematics Experience with industrial communication interfaces Experience with safety system design including functional safety components and safety architectures   We are looking forward to receiving your detailed application including motivational statement and diploma copies . We only accept applications through our online career portal. Applications via e-mail or 3rd party platforms will be deleted due to GDPR regulation. You can track your application statushere. Your application may be considered for other open positions. Altran only accepts direct applications (no recruitment agencies). For more information contact directly our Talent Acquisition Manager,Mark Swerissen.
Inserat ansehen

15.03.2020

Altran Switzerland AG

Embedded SW Engineer

  • Altran Switzerland AG

  • 8058Zürich

  • 15.03.2020

  • Vollzeitstelle

Job TitleEmbedded SW Engineer Vacancy Reference Number21826 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer We are looking for a technically experienced embedded SW developer joining our electrical engineering team. Your role Responsible for the entire SW development life cycle (SDLC) including requirements engineering, design, implementation, system testing and maintenance Handle software configuration management and build processes Maintain existing software and test infrastructure Develop software components and drivers for embedded systems Automate system and integration tests Integration of Matlab/Simulink components on a target ARM architecture Your profile MSc. degree in Electrical Engineering, Electronics or Mechanical Engineering Several years of practical industry experience combined with deep knowledge of embedded systems Proficient in C and C++ programming Experience with Matlab / Simulink Knowledge about m- and tlc scripts Experience with embedded OS (e.g. Linux, VxWorks) is advantageous Strong software design and architecture knowledge Fluent in English, German is a plus   We are looking forward to receiving your detailed application including motivational statement and diploma copies . We only accept applications through our online career portal. Applications via e-mail or 3rd party platforms will be deleted due to GDPR regulation. You can track your application statushere. Your application may be considered for other open positions. Altran only accepts direct applications (no recruitment agencies). For more information contact directly our Talent Acquisition Manager,Mark Swerissen.
Inserat ansehen

13.03.2020

Altran Switzerland AG

Qualification & Validation Engineer (German speaker)

  • Altran Switzerland AG

  • 8058Zürich

  • 13.03.2020

  • Vollzeitstelle

Job TitleQualification & Validation Engineer (German speaker) Vacancy Reference Number20917 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer A permanent contract with the leader in innovation and high-tech engineering consulting A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D). In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva. Your role Foster innovation and continuous improvement on process, and on Qualification and Validation projects Maintain equipment to support GMP manufacturing ensuring all equipment comply with Standard Operating Procedures and Policies (SOPs) Collaborate to create user requirements (URS) Build validation and qualification plans Creation of plant structures (units and functional locations) Establish and review DQ, IQ, OQ and PQ documents Participation in GMP relevance and risk analyses Responsible for the administration of qualification work (pending tasks, CAPAs, etc.)  Ensure that all validation activities are carried out and reported in a timely manner. Your profile BSc/MSc degree in Engineering or Chemistry Minimum 3 years of experience in Qualification / Validation in the Pharmaceutical industry Applied knowledge of FDA and international Pharmaceutical regulations is preferred Applied technical understanding of manufacturing equipment (autoclaves, washing machines...); processes specific to Pharmaceutical manufacturing preferred Applied Knowledge of creation and verification of qualification equipment plans (FAT/SAT/DQ/IQ/OQ/PQ) Languages: fluent in English AND German
Inserat ansehen

12.03.2020

Altran Switzerland AG

Development Quality Manager

  • Altran Switzerland AG

  • 8012Zürich

  • 12.03.2020

  • Vollzeitstelle

Job TitleDevelopment Quality Manager Vacancy Reference Number20286 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer We offer: - A permanent contract with the leader in innovation and high-tech engineering consulting - A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D) - In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva Your role Purpose: The Development Quality Manager is responsible for Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GPvP) oversight and for assuring quality and compliance of Development and Medical Affairs (MA) projects, products and programs (Phase I through Phase IV), as well as GxP activities related to Marketing. Ensure in direct support, collaboration and partnership with the Clinical Studies Department, Medical Department, Patient Safety, Regulatory Affairs and Marketing Departments the implementation of the Quality Management System in the Country Organization to achieve a high level of quality and compliance.   Major Activities: - Audit management: o Provide guidance for the preparation, conduct and follow-up of GCP and Pharmacovigilance (PV) related audits. - Inspection management: o Provide support prior to, during and after health authority (HA) inspections within country organization and at investigational sites. o Ensure that responses to local HA have been submitted, commitments have been met and relevant actions plans have been completed/closed. - Deviations and Issues Management: o Ensure that deviations and issues are properly managed in the internal tracking system including the respect of the escalation process. o Support the investigation process (root cause analysis, action plan development) as appropriate. - Management of vendors in the GCP / PV area as well as for Patient Oriented Programs (POPs): o Perform (re-)qualification of vendors in the GCP / PV area as well as for external service providers involved in Patient Oriented Programs (POPs). - Release activities: o Perform the release of Investigational Medicinal Products for clinical trials, investigator-initiated trials and managed access programs. o Ensure that all IMP release-related documents are filed in the related database. o Keep oversight of release activities. - SOP Management: o Support the implementation of global SOPs to local Quality Management System. o Review and update local SOPs, Working Practices and Forms. Your profile Requirements: Education: Degree in Life Sciences or related fields Languages: German / English fluent in speaking and writing Experience: Min. 3 years’ experience in the pharmaceutical industry in a relevant field such as quality assurance, pharmacovigilance, clinical development or a directly related area Additional Requirements: Strong project management skills, GCP und PV knowledge   Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland.
Inserat ansehen

09.03.2020

Altran Switzerland AG

Engineer Aircraft System Safety

  • Altran Switzerland AG

  • 8012Zürich

  • 09.03.2020

  • Vollzeitstelle

Job TitleEngineer Aircraft System Safety Vacancy Reference Number22239 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer For our current customer project in the Lucerne region, we are looking for a qualified and experienced engineer for our on-side aviation team as an aircraft system safety engineer with focus on Service Life Assessment Program for Structural Parts Recertification of aircraft. Your role Assume responsibility for analysis of structural parts with the additional view of the overall system level over the entire life cycle  Establish the lifing analysis process and document templates  Coordinate the work between structural design and system engineering (i.e. responsible for system safety)  Prepare optimized workflow and tools such as document templates  Mitigate option assessment for structural parts regarding life cycle including review of technical, logistical and financial considerations and impacts  Release recommendations as replacement, retrofit modification or safety by inspection  Risk assessment (hazard severity an probability) and recommendations on a part level / view of the overall system level Your profile MSc. in Mechanical Engineering or Aerospace Engineering  Min. 3 years of practical industry experience in this project field Experience in Aircraft System Safety (e.g. MIL-STD-882), structural engineering (FEM, design etc.) and fatigue and damage tolerance analysis Fluent in English, German (at least B2) and Swiss German is a plus Proactive approach including willingness to push forward and take decisions   We are looking forward to receiving your detailed application including motivational statement and diploma copies . We only accept applications through our online career portal. Applications via e-mail or 3rd party platforms will be deleted due to GDPR regulation. You can track your application status here. Your application may be considered for other open positions. Altran only accepts direct applications (no recruitment agencies). For more information contact directly our Talent Acquisition Manager, Mark Swerissen.
Inserat ansehen

07.03.2020

Altran Switzerland AG

Design Engineer Aviation

  • Altran Switzerland AG

  • 8058Zürich

  • 07.03.2020

  • Vollzeitstelle

Job TitleDesign Engineer Aviation Vacancy Reference Number21587 Work SiteSwitzerland / | CHE - All Regions / Zürich Contract TypePermanent [Full-Time] Minimum number of years of experience required2 years of experience and more Our offer The Global Industry Team in Zurich is looking for a passionate and hands-on design repair engineer supporting our aviation team in central Switzerland. Your role Establish repair design and validation substantiation requirements for technical dialog or engineering authorizations relating to repairs and alterations Participate in a multi-discipline team Support Repair Disposition and Reviews Provide ESW suggestions to continuously improve our repair design process Support the Customer in the resolution of field supportability issues Your profile MSc. or BSc. in Mechanical, or Aerospace Engineering Minimum 5 years of industry experience Defense industry experience is a plus Experience in CATIA V5 Experienced in design metallic and composite light weigh structures Knowledge and experience in repairs of aircraft metallic and composite structures Experienced in aeronautical field preferred Eligible to work in Switzerland (visa B or C) Excellent communication and coordination skills Language skills: German (B1) and English fluently   We are looking forward to receiving your detailed application including motivational statement and diploma copies . We only accept applications through our online career portal. Applications via e-mail or 3rd party platforms will be deleted due to GDPR regulation. You can track your application statushere. Your application may be considered for other open positions. Altran only accepts direct applications (no recruitment agencies). For more information contact directly our Talent Acquisition Manager,Mark Swerissen.
Inserat ansehen