Regulatory Affairs & QA Specialist for IVD Medical Devices
PARIS, 75
il y a 6 jours
Advanced Biological Laboratories seeks a Full-time Medical Device Regulatory Affairs and QA specialist to join the Governance, Risk and Compliance (GRC) team. The role focuses on ensuring regulatory compliance and quality for medical devices, including standalone software and reagents.
Candidates should have 3–5 years in med-tech, with ISO 13485:2016 and EN ISO 14971:2012 experience, and knowledge of EU MDR regulations. Fluent English and cross-functional collaboration are required.
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Entreprise
Advanced Biological Laboratories
Plateforme de publication
WHATJOBS
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