Quality Compliance Lead — Medical Devices; ISO13485 & Audits
Listed on 2026-10-10
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Quality Assurance - QA/QC
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Healthcare
Medical Science, Data Scientist
Location: Keele
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.
The Quality Compliance Lead — Medical Devices (ISO
13485 & Audits) role at Biocomposites is now open for applications in Keele, England, United Kingdom.
We are seeking a motivated Quality Compliance Lead — Medical Devices (ISO
13485 & Audits) to join Biocomposites in Keele, England, United Kingdom.
Consider building your career as a Quality Compliance Lead — Medical Devices (ISO
13485 & Audits) at Biocomposites.
The Quality Compliance Lead — Medical Devices (ISO
13485 & Audits) position in the Bio & Pharmacology & Health, Management & Operations field is open for applications.
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