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Manager/ Senior Manager Regulatory Affairs Cmc jobs at Incyte in Switzerland
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18 jobs found
15.12.2024
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Incyte Senior Director/ Director Clinical Research Scientist Switzerland, Vaud
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Development of protocols for clinical studies. Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans. Drafting and review of clinical...
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14.12.2024
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Incyte Manager/ Senior Manager Regulatory Affairs CMC Switzerland, Vaud
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Ensures regulatory guidance documents and laws, as well as internal policies and procedures, are followed to ensure regulatory compliance is maintained. In alignment with RA-CMC leader, supports / manages regulatory...
15.09.2024
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Incyte Technician / Senior Laboratory Analytical Switzerland, Vaud
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The Technician / Senior Technician Laboratory and Analytical implements analytical methods for new products, generates the corresponding analytical documentation and executes the different analytical analyses to support the execution of...
15.09.2024
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Incyte Technician / Senior Laboratory Analytical Switzerland, Vaud
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The Technician / Senior Technician Laboratory and Analytical implements analytical methods for new products, generates the corresponding analytical documentation and executes the different analytical analyses to support the execution of...
28.08.2024
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Incyte Senior Medical Director Global Risk Management & Safety Surv... Switzerland, Vaud
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Lead the Safety Management Team and direct all safety risk management activities for assigned products. Ensure local and global risk management plan preparation and execution throughout a medicinal product’s lifecycle....
27.08.2024
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Incyte Senior Director Head IAI Medical Affairs Region Europe Switzerland, Vaud
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Leads European cross functional strategy at GPT with full accountability for all IAI assets. As head of IAI Medical Affairs Region Europe, leads & drives EU medical strategy and communications...
16.07.2024
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Incyte Senior Engineer Quality Assurance CSV Switzerland, Vaud
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Manage the day-to day quality oversight of GxP IT, Computerized System Validation (CSV) and Automated and Computerized systems (SISA) related activities. Act as the main point of contact for all...
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Description:Full job details
Development of protocols for clinical studies. Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans. Drafting and review of clinical...
These jobs might be a good fit
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