About this role
Senior Regulatory Affairs Specialist at Osv-bioventus. Location: Durham, North Carolina, United States. Role: authoring submissions, maintaining documentation, performing assessments Requirements: Master's in regulatory affairs or related plus 3+ years regulatory experience in medical devices; experience with 510(k)/PMA, EU MDR/MDD, regulatory assessments, project management, and cross-functional/regional submissions. Category: Legal and Compliance Seniority: Mid Level Commitment: Full Time Workplace: Hybrid Languages: Mongolian, English