Stellenangebote für Jobs in Eysins

13.05.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 80’000 - CHF 100’000 Funktionale Zielsetzung Diese Position ist in erster Linie für die Qualitätssicherung und das Qualitätsmanagement verantwortlich, um sicherzustellen, dass Biosimilars-Produkte gemäß den aktuellen Good Manufacturing Practices und anderen geltenden Vorschriften in den operativen Einheiten von Freseni

12.05.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 125’000 - CHF 150’000 Director Corporate Patent Counsel (all genders), Eysins Client Location Job Category Other Job Reference 1993271de21e Job Views 3 Posted 02.04.2025 Expiry Date 17.05.2025 Job Description Director, Corporate Patent Counsel We are looking for an experienced European or US patent attorney to st

01.05.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 150’000 - CHF 200’000 Senior Director, Quality Management, EMI OUS Operations & OEM you will be responsible for developing and maintaining quality assurance programs, policies, procedures, and controls for pre-production supplier qualification, capability development, and manufacturing quality for both internal OUS (Outs

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 F

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 the

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 auth