09.05.24 | Vollzeit | Sort-en-Chalosse | Michael Page InternationalEnsure the regulatory compliance of medical devices in various markets worldwide. Anforderungsprofil - Previous experience (preferably 3-5 years) in the management of Instructions For Use for medical devices or drugs. - Familiarity with the structure of technical documentation and proficient in using
Später ansehen09.05.24 | Vollzeit | Sort-en-Chalosse | Michael Page InternationalProcesses management - - Support in post-market surveillance activities - - Medical device data management, creation and maintenance of associated documentation - - Support in QMS improvements and audits - - Ensure regulatory compliance and process optimization - - Cross-functional collaboration and advice
Später ansehen09.05.24 | Vollzeit | Sort-en-Chalosse | Michael Page Internationaldocumentation 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 device; - Review and approval of validation and verification documents; - Acting as Process Owner; - Contribution to internal
Später ansehen28.03.24 | Vollzeit | Lausanne | Randstad Schweiz AGCompliance/Quality system roles. - A Bachelor’s or Master’s degree in medical technology, life sciences, or a related field (or equivalent work experience). - Experience in documentation control and record management is preferred. - Excellent organizational, problem-solving, and interpersonal skills
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