MedTech Quality & Regulatory Lead, Hybrid

A Med Tech firm in the UK is seeking a Quality & Regulatory Officer to lead compliance, manage the Quality Management System (QMS), and oversee global regulatory submissions. This role involves maintaining ISO 13485 standards, managing audits, and ensuring compliance with EU MDR and FDA requirements. The ideal candidate will have proven experience in Medical Device regulatory affairs, strong knowledge of applicable regulations, and excellent organisational skills.

This position requires on-site work three days a week, offering an opportunity to contribute significantly to international market growth.
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