Global Regulatory Affairs Specialist, Medical Devices

2 days ago


Greater London, United Kingdom Story Terrace Inc. Full time

A leading health technology company in Greater London is seeking a Regulatory Affairs Specialist. This role involves supporting regulatory pathways for medical devices and ensuring compliance with global standards. You will collaborate across teams, prepare regulatory submissions, and monitor evolving requirements. Ideal candidates have 3–6 years of experience in regulatory affairs within the medical device sector, with strong analytical and communication skills. A commitment to impactful work in a fast-paced environment is essential.
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