MedTech QA & Regulatory Specialist – ISO 13485

Newton Colmore Consulting Ltd is looking for a Quality Assurance & Regulatory Affairs Specialist to join a growing medical devices company based in Cambridgeshire. The successful candidate will develop quality assurance strategies, ensure compliance with ISO 13485, and conduct internal audits.

This full-time office position offers a competitive salary package, company pension scheme, and additional benefits including free lunches. Ideal candidates will have a background in engineering or biomedical engineering, with 2 to 5 years of experience in the medical device industry.

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