23.05.24 | Vollzeit | Vaud | Michael Page InternationalDevices About Our Client Our client is an international company specialized in medical devices. Job Description - Technical documentation writing management (for Europe & the US); - Involvement in the development and design of the company's medical devices; - Risk management, from the early life of each
Später ansehen23.05.24 | Vollzeit | Zug | Michael Page InternationalAnd maintenance of the LAB (as needed) - Creating documentation required to comply with established processes (as needed) - NOTE Depending on the experience and seniority level tasks can be extended with a focus on mechanical testing of packaging products such as auto-injectors or pen injectors The Successful
Später ansehen21.05.24 | Vollzeit | Schaffhausen | Randstad Schweiz AGAnd services to advance the health and well-being of people. Cilag AG is an international manufacturing company of the Janssen pharmaceutical division of the Johnson & Johnson Group and produces pharmaceutical and medical device products as well as active chemical ingredients (APIs) for global markets at its
Später ansehen20.05.24 | Vollzeit | Hays AGO Technical support in computerized system validation projects (CSV) o IT Business continuity & disaster recovery, backup and restore o Change and incidence management and technical documentation (e.g. SOP) o Archive of electronic data according to GXP principles o Participation in inspections
Später ansehen08.05.24 | Vollzeit | Lugano | Randstad Schweiz AGAnd cosmetic treatments. 6. Work closely with other healthcare professionals to provide comprehensive care. 7. Maintain patient records and documentation in accordance with medical and legal requirements. 8. Stay updated with the latest dermatological practices and research to provide evidence-based care
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 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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