Global Regulatory Affairs Specialist: FDA

2 weeks ago


South Yorkshire, United Kingdom Aurora Lifesciences Full time

A medical device company in South Yorkshire is seeking a Regulatory Affairs Specialist to support global regulatory strategies and ensure compliance with FDA and EU MDR frameworks. The role involves managing regulatory filings, ensuring compliance, and collaborating across teams. The ideal candidate will have 3–5 years of regulatory affairs experience in the medical device industry, strong communication skills, and a solid understanding of applicable standards.
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