About this role
Sr. Regulatory Affairs Specialist at Osv_bioventus. Location: Durham, North Carolina, United States. Role: author submissions, maintain technical files, conduct assessments Requirements: 5 years Regulatory Affairs in medical devices; FDA/EU registrations; Bachelor’s in Life Sciences or Engineering. Category: Research and Development (R&D) Seniority: Senior Level Commitment: Full Time Workplace: Onsite Languages: English