About this role
IVD Assessor at MHRA. Location: London, England, United Kingdom. Role: reviewing applications, liaising teams, providing input Requirements: Master's degree in a relevant discipline, extensive experience in IVD policy/product development or conformity assessment, laboratory and clinical device experience, expert knowledge of UK MDR, EU IVDR/EU MDR and clinical trial regulations. Category: Research and Development (R&D) Seniority: Senior Level Commitment: Full Time Workplace: Hybrid Languages: English