Part-Time Medical Device QA & Regulatory Lead (Class I)

West Sussex based medical device organisation is seeking a Senior Quality & Regulatory Affairs Specialist on a part-time basis (2.5 days per week). The role focuses on maintaining quality and regulatory compliance for a Class I(s) medical device, with outsourced manufacturing, and involves supplier oversight, documentation, audits and post-market surveillance.

Candidates should have 5+ years in QA/Regulatory Affairs for medical devices, with ISO 13485 knowledge and UK/EU regulatory exposure.

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