Senior Regulatory Affairs Lead – Global Medical Devices

Smith+Naphew, based in Hull, is seeking a Senior Regulatory Affairs Specialist to lead regulatory activities for wound management products and ensure global compliance. The role collaborates with cross-functional teams to guide development, changes, and launches, driving registrations and approvals worldwide.

You will work in a hybrid setup, ensuring adherence to ISO 13485, FDA 21 CFR Part 820, and cGMP/cGDP standards while supporting continuous improvement and knowledge sharing across the team.

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