Medical Device QMS Auditor (ISO 13485, MDR)
London
Our client is a fast-growing, well-funded company authorised to assess and certify medical devices, combining clinical, technical and regulatory…
TÜV Rheinland Europe is seeking a Medical Device Assessor/Auditor with a background in medical device design, manufacturing, or quality control. The role involves planning and conducting audits at client sites, reviewing documentation, and ensuring regulatory compliance.
Candidates should hold a technical degree and have at least four years of relevant experience, with ISO 13485 knowledge and willingness to travel internationally.
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