Medical Device Quality & Regulatory Consultant

PA Consulting, based in the UK, seeks an experienced Medical Device Quality Specialist Consultant to support quality systems, regulatory compliance, and lifecycle management of medical devices and combination products. You will work with multi-disciplinary teams across ISO 13485, 21 CFR Part 4, FDA, UK MDR and EU MDR requirements.

You’ll lead regulatory submissions, risk management (ISO 14971), supplier quality, CAPA, and post-market activities, contributing to development from early stages

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