12.05.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 125’000 - CHF 150’000 To strengthen our pharma patents team at Merck in Eysins, Switzerland (Lake Geneva area). As a member of cross-functional teams, you shape the global IP strategy for pharmaceutical development projects and commercial products. This includes building and defending patent portfolios, managing freedom to operate
Später ansehen01.05.25 | 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
Später ansehen27.04.25 | 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 ansehen03.04.25 | Vollzeit | Eysins | Randstad Schweiz AGPerformance indicators that enable data-driven decisions. Additionally, you will contribute to the development and execution of strategies for new product launches and product line extensions, ensuring smooth, timely execution. Who you are - University degree or equivalent in Supply Chain Management, APICS
Später ansehen11.03.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 80’000 - CHF 100’000 Requirements are met along the assigned project development work. - Keep up to date with the latest regulatory CMC requirements through regulatory surveillance. Coordinate timely implementation of any changes or new relevant laws or guidance; provide comments on new laws on behalf of FK-SBS through
Später ansehen30.01.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 80’000 - CHF 100’000 In the Biotech Industry with demonstrated track record in Upstream processing for biologics, preferably with mammalian cell culture and monoclonal antibody experience; previous experience working with biosimilars would be also an advantage - Strong technical expertise across the Upstream development spectrum
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