Team Leader Regulatory Affairs Manager Chemistry (all genders) – 100% für Gi Life Sciences Basel in Zuchwil - myjob.ch
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      12.06.2026

      Team Leader Regulatory Affairs Manager Chemistry (all genders) – 100%

      • Zuchwil
      • Festanstellung 100% | Führungsposition

      • Merken
      • drucken
       

      Gi Life Sciences Basel

      Gi Life Sciences Basel

      Team Leader Regulatory Affairs Manager Chemistry (all genders) – 100%

      Your Responsibilities

      • Providing both technical and personnel leadership for the Regulatory Affairs department
      • Acting as deputy to the Director RQS
      • Ensuring global regulatory compliance of products based on expert knowledge and collaboration with local stakeholders, including:
        • Maintaining worldwide REACH compliance, including substance registrations, exposure scenarios, compliance documentation, and supply chain communication
        • Classifying substances and mixtures according to CLP regulations and international regulatory requirements, taking harmonized classifications and local legislation into account
        • Creating, maintaining, and managing Safety Data Sheets (SDS) for existing and new formulations in line with international standards, and ensuring availability for production, laboratories, and customers
        • Coordinating and implementing GHS reclassifications, including updates to labels and systems, while assessing the impact on product regulatory compliance
      • Communicating with relevant authorities and serving as the designated contact person for chemical regulations
      • Supporting development projects by integrating regulatory requirements at an early stage
      • Acting as system owner for the chemical database, including maintenance, change assessments, and continuous improvements
      • Creating and maintaining formulations and products in ChemGes software, as well as managing related ERP master data

      Your Profile

      • Degree in Chemistry, Pharmacy, or a related scientific field
      • Strong regulatory expertise in chemicals legislation (e.g., CLP/GHS, REACH, dangerous goods regulations); knowledge of medical devices is an advantage
      • Familiarity with quality management systems such as ISO 9001 and ISO 13485
      • Proven experience in stakeholder and interface management, including communication with regulatory authorities
      • Leadership experience, including team development and fostering a feedback culture
      • Experience in scientific and regulatory writing
      • Fluent German and English skills (B2–C1 level)
      • Basic IT and system knowledge

      Arbeitsort: Zuchwil