About this role
Senior Regulatory Affairs Specialist at Medtronic. Location: Bucharest, Bucharest, Romania. Role: coordinating documentation, overseeing vigilance, monitoring regulations Requirements: Bachelor's in Medicine/Pharmacy/Bioengineering/Chemistry, 3+ years regulatory affairs experience (medical devices preferred), fluent English, experience with regulatory submissions, post-market vigilance, MDD/MDR transition, and stakeholder engagement. Category: Legal and Compliance Seniority: Mid Level Commitment: Full Time Workplace: Hybrid Languages: English