Global Regulatory Affairs Specialist Medical Devices

Position: Global Regulatory Affairs Specialist for Medical Devices
A growing medical device company is seeking a Regulatory Affairs Officer based near Edinburgh, UK. The chosen candidate will build regulatory strategies, manage product license registrations globally, and ensure compliance with various regulatory requirements, including ISO standards and FDA regulations. Responsibilities include advising staff on submissions, preparing documentation, and liaising with regulatory authorities.

This role offers a dynamic work environment and flexible benefits, encouraging innovation and customer focus.
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