Freelance Regulatory Affairs Consultant — EU MDR
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Barrington James Limited is seeking an experienced Regulatory Affairs Consultant for a freelance contract in Belgium. You will lead regulatory submissions, develop strategies, and ensure EU MDR compliance for medical devices across cross-functional teams.
The role emphasizes strong submission management, conformity assessment knowledge, and stakeholder communication in a collaborative environment. Fluency in English is essential; additional European languages are advantageous.
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