03.05.24 | Vollzeit | Uster, Zug, Dübendorf, Dietiko | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Emmen, Zürich, Frauenfeld, Kri | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen06.05.24 | Vollzeit | Zürich | NonStop Consulting | Foothold in the industry, our client has a track record of successful projects and continuous growth, providing a solid foundation for professional advancement. Benefits Engage with top players in the automotive sector Longterm career prospects with ongoing personal development opportunities
Später ansehen19.01.24 | Vollzeit | JobLeads GmbH | CHF 150’000 - CHF 200’000 Applications that so far were beyond reach (see our case studies in,,). Our customers are large asset operators and service providers of industrial plants pioneering robotics technology for inspection and maintenance. Our solution enables autonomous routine inspections and monitoring of large-scale
Später ansehen02.05.24 | Vollzeit | Bern | Randstad Schweiz AGBased viral- and bacterial vaccines and bacterial based therapeutic products. Main Responsibilities - Ensure the GMP-compliant production of active ingredients and drugs for clinical trials and market launch by organizing, coordinating, and tracking personnel training and qualification - Define
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