09.05.24 | 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 International& external audits; - Ensure strong collaboration with other teams, and supporting them in QA/RA trainings. Anforderungsprofil - Minimum 3 years of experience within the medical device industry; - Strong knowledge of ISO 13485, ISO 14971, 21 CFR, MDR; - Experience with submitting technical files for Europe
Später ansehen09.05.24 | Vollzeit | Nyon | Michael Page InternationalAnd invoicing. - Manage office supplies and coordinate the logistics of corporate events. - Assist in organizing sporting events and member assemblies. - Collaborate with internal and external contacts, such as auditors and financial advisors. - Ensure adherence to the association's regulations and internal
Später ansehen09.05.24 | Vollzeit | Genève | Michael Page InternationalWith FDA requirements - Coordinate the responses to questions raised by FDA - Review of product labelling - Participate in audits and inspections, ensuring compliance with FDA requirements - Stay up-to-date with relevant regulations, guidelines, and industry trends, and provide strategic regulatory
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