01.05.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 150’000 - CHF 200’000 And influence a quality culture. - Multi-BU authority and accountability for developing, deploying, and maintaining a robust and compliant quality management system for the design, risk management, and ongoing life-cycle maintenance of BD products. - Actively identify improvements to the processes within
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 ansehen19.04.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 80’000 - CHF 100’000 Respected spokesperson during interactions. 5. Prior experience working with connected drug/device combination products for medicinal products is desirable. 6. Good understanding of the clinical development process, trial design aspects, and relevant clinical regulatory frameworks such as ICH, GCP, MDR
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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