Global Regulatory Affairs Specialist – Medical Devices

Global Regulatory Affairs Specialist – Medical Devices

Full-Time On-site
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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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Global Regulatory Affairs Specialist – Medical Devices employer: Advanced Medical Solutions

Advanced Medical Solutions is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration. With a strong focus on employee growth, you will have access to ongoing training and development opportunities while working in a field-based role that allows you to make a meaningful impact across NHS and private healthcare organisations in the UK.

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Contact Details:

Advanced Medical Solutions Recruitment Team