03.05.24 | Vollzeit | Frauenfeld, Schaffhausen, Dübe | Daiichi Sankyo Europe GmbHdocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen24.04.24 | Vollzeit | Sempach, Sempach Stadt | Randstad Schweiz AGFor our client specialized in Medical Device area, we're looking for a Product engineer administrator Location Lucern canton Position Permanent You will play a crucial role in maintaining and managing SAP basic data in the product engineering domain. You will be responsible for creating
Später ansehen17.04.24 | Vollzeit | Pratteln | JobLeads GmbH | CHF 200’000 - CHF 250’000 And maintain comprehensive IT documentation and procedures. Santhera Pharmaceuticals (SIX SANN) is a Swiss specialty pharmaceutical company focused on the development and commercialization of innovative medicines for rare neuromuscular and pulmonary diseases with high unmet medical need. • Continuous
Später ansehen04.11.19 | Vollzeit | Zürich | Ava AGAs the best Swiss startup in 2017 and 2018. Our current key markets include USA, Germany, Switzerland and UK. Would you like to join us on our challenging adventure? Responsibilities - Develop clinical trials in women’s health from A to Z (e.g. trial design, statistical analysis plan, clinical documentation
Später ansehen31.10.19 | Vollzeit | Bern | Decomplix' ISO 13485 quality management system. - supporting our customers in quality management. - customer support on their regulatory path (pre- and post-market). - project management to bring the technical documentation of customer products to the point where they can obtain the CE mark for medical devices
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