Global Regulatory Lead – Medical Devices (EU MDR/US FDA)

Cure Talent is thrilled to partner with a global medical device company seeking a Regulatory Affairs Lead in Crewe. This hands-on role involves supporting regulatory activities, with a focus on document review and international registrations. Candidates should have proven experience in Regulatory Affairs and familiarity with EU MDR and US FDA frameworks.

The successful candidate will oversee regulatory strategy, perform comprehensive document reviews, and guide submissions across various markets. Mentorship within a small team will also be part of the responsibilities.

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