24.04.24 | Vollzeit | Rüti | NonStop Consulting | CHF 80’000 - CHF 85’000 / Jahr pharmaceuticals, beverages, and specialty products, contributing to a brighter future. The Role - You are responsible for checking feasibility, preparing quotations and documentation in accordance with customer requests. - You ensure timely order processing in terms of adherence to deadlines, quality and costs
Später ansehen30.03.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 150’000 - CHF 200’000 Which consists of approximately 20 employees, including laboratory technicians and GMP staff in QA, QC, PM positions. You will report directly to the Head of Hevesy Laboratory. Responsibilities - People management as team leader for production and GMP staff. - Lead and supervise the production, quality
Später ansehen25.03.24 | Vollzeit | Thörishaus | Bavarian Nordic Berna GmbHIn Engineering, Biotechnology, or related mum of 5 years relevant experience in a GxP regulated pharmaceutical/biotechnology mum of 3 years validation and qualification experience requiredSolid computer skills including MS Office ytical thinking and problem-solving
Später ansehen22.03.24 | Vollzeit | Uster, Frauenfeld, Zug, Dietik | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Schaffhausen, Dübendorf, Krien | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Dietikon, Uster, Luzern, Züric | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Emmen, Zürich, Luzern, Dietiko | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Schaffhausen, Dübendorf, Krien | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Luzern, Emmen, Zürich, Dietiko | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Dietikon, Uster, Luzern, Züric | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
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