Global Regulatory Affairs Specialist – Medical Devices

Advanced Medical Solutions in Winsford, England, United Kingdom, is seeking a Regulatory Affairs Associate to manage regulatory documentation for EU and US markets and other territories. You will support submissions, maintain DHF, review risk management, engage with authorities, and drive post-market surveillance and compliance improvements across product life cycles.

The role requires strong knowledge of MDR, 510(k), ISO 13485, and QMS processes, with ability to coordinate with cross-functional

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