Quality Compliance Lead — Medical Devices (ISO13485 & Audits)

Biocomposites Keele is seeking a Quality Compliance Lead to own the QMS/eQMS and ensure regulatory compliance with ISO 13485, MDSAP, GMP and FDA standards. You will lead internal audits and drive continuous improvement.

You will manage a quality team, develop training, review documentation, and support supplier and regulatory audits. Some travel is required to support global operations in a fast‑moving medical devices environment.

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