19.09.24 | Vollzeit | Val-d'Illiez | WuXi AppTecOf contact for QA, Compliance, Quality Supplier, and Regulatory Affairs. - Act as the point of contact with customer for quality topics, coordinates response - notification to the client related to quality topics - Coordinate and drive quality activities related to - Technology tech transfer, - Analytical
Später ansehen18.09.24 | Vollzeit | Zürich | JobLeads GmbH | CHF 100’000 - CHF 125’000 This role is for one of the Weekday's clients. What You’ll Do As a Manager of Regulatory Affairs, you'll oversee regulatory activities for our medical products. Your responsibilities include - Ensuring compliance with regulatory requirements during product design, development, production, and post
Später ansehen18.09.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 80’000 - CHF 100’000 Director Switzerland & BU International API with a functional reporting to the Director of Technical Support API & Pharma Compliance. Your tasks and responsibilities - The role combines two aspects the Technical Support to Regions (TSR-API), which entails addressing any Regulatory Affairs and Quality
Später ansehen19.09.24 | Teilzeit, Vollzeit | Genève, Sort-en-Chalosse, Base | Michael Page InternationalVerkaufsadministrator (m/w) 1 - Healthcare & Life Sciences 11 - Biotechnologie 3 - Klinischer Betrieb 2 - Medical devices 2 - Pharma-Industrie 2 - Regulatory Affairs 2 - Technologie 8 - IT Business Analyst (m/w) 2 - IT Support 2 - System Adminstrator (m/w) 2 - ERP 1 - IT Projekt & Program Management 1 - Logistik
Später ansehen19.09.24 | Vollzeit | Michael Page Internationalaffairs across multiple countries and will collaborate with finance teams to efficiently handle the period-end closing process. - Save Job - added 10/09/2024 - Modern Workspace and environment - English only needed (German is a plus) About Our Client The client is a renowned, international Hospitality
Später ansehen19.09.24 | Vollzeit | Vaud | Randstad Schweiz AGQuality standards. Main Tasks - Provide expertise in mAbs/protein analytics to deliver high-quality analytical packages supportingthe company's product development that meet Global Health Authority requirements, particularly in the US and EU. - Work closely with CMC Development Teams, Regulatory Affairs
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