About this role
RAQA Manager at Chipiron. Location: Paris, Île-de-France, France. Role: defining strategy, overseeing submissions, building QMS Requirements: 3+ years QA and regulatory affairs experience in medical devices; medical/scientific background; knowledge of ISO 13485, FDA regs, IEC 62304/60601, ISO 14971; fluent English and French. Category: Research and Development (R&D) Seniority: Mid Level Tools: ISO 13485, FDA regulations, IEC 62304, ISO 14971, IEC 60601 Commitment: Full Time Workplace: Hybrid Languages: English, French