PA Consulting is seeking an experienced Medical Device Quality Specialist Consultant to support the development and lifecycle management of medical devices and combination products. You will help clients navigate regulatory complexity, embed robust quality systems, and ensure product safety and compliance from development through post‑market.
Ideal candidates have 8+ years in the medical device field, consultancy experience, and strong knowledge of ISO 13485, 21 CFR Part 4, FDA, UK MDR and EU
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