Senior Global Regulatory Lead – Medical Devices (Hybrid)

Smith+Nebhew in Hull is seeking a Senior Regulatory Affairs Specialist to manage regulatory submissions, ensure compliance across the product lifecycle, and support global market access for Advanced Wound Care products.

You will partner with cross-functional teams, liaise with authorities, and drive ISO 13485, FDA 21 CFR Part 820, cGMP and cGDP compliance while enabling successful product launches.

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