12.05.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 125’000 - CHF 150’000 Experience would be an advantage. - Knowledge of biological manufacturing processes would be an advantage. - Sound understanding of the regulatory framework for pharmaceuticals would be an advantage. - You take ownership of your work and its impact on our business. - You are a strong communicator and a team
Später ansehen01.05.25 | 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 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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