Stellenangebote für Manager Jobs in Eysins

01.05.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 150’000 - CHF 200’000 Manufacturing and ISO standards, you possess - Deep knowledge of medical device and pharmaceutical regulations such as MDD/MDR, IVDD/IVDR, MDSAP, CMDR, ISO 13485, J-PAL. - Outstanding project management and organizational skills. - A track record of managing multiple projects simultaneously. - The ability

27.04.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 80’000 - CHF 100’000 Functional Goal This position has primary responsibility for providing Quality Assurance and Quality Management Oversight to ensure that biosimilars products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices and other applicable regulations within

19.04.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 80’000 - CHF 100’000 Senior Manager, Regulatory, Digital Health and Device (all genders), Eysins Client Location Job Category - Job Reference fc03f4e4d2a6 Job Views 3 Posted 02.04.2025 Expiry Date 17.05.2025 Job Description We are looking for an experienced person to take the position of Senior Manager

03.04.25 | Vollzeit | Eysins | Randstad Schweiz AGThe lead in developing and executing supply plans that align with both global business objectives and local market demands, while considering the requirements of internal and external manufacturing sites. Collaborating closely with demand planning teams, you will manage inventory levels and replenish

11.03.25 | 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

30.01.25 | 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