27.04.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 80’000 - CHF 100’000 And CP. Main Tasks - Maintain an up-to-date knowledge of cGxP regulation and applicable standards (especially in the US and EU) and implement requirements into locally applicable procedures (SOPs, Guiding Documents, Working Instructions, etc); - Support a GMP compliant transition of Programs from
Später ansehen11.03.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 80’000 - CHF 100’000 MAIN TASKS - For the assigned products/programs, define and execute an RA-CMC Strategy that best serves the biosimilars business needs and ensure compliance with regulatory systems. - Manage Change Controls evaluation; The preparation and finalization of Quality regulatory documents which form
Später ansehen30.01.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 80’000 - CHF 100’000 Main Tasks - Oversee and guide outsourced (CDMO) upstream process and cell bank related activities around the technical development, approval and life cycle management of Biosimilar drug substance production; including process tech transfer, GMP manufacturing of drug substance, IND application
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