About this role
Head of QARA at Raidium. Location: Paris, Île-de-France, France. Role: Lead regulatory, Manage submissions, Maintain QMS Requirements: At least 3 years in Regulatory Affairs/Quality Assurance for medical devices; Master’s degree in Life Sciences, Engineering, Law, or related field; MDR/FDA experience; ISO 13485 familiarity; authorization to work in France; fluent in English. Category: Legal and Compliance Seniority: Senior Level Certifications: iso 13485 Commitment: Full Time Workplace: Onsite Languages: English, French