About this role
Sr Regulatory Affairs Specialist International at Osv-bioventus. Location: Amsterdam or United Kingdom. Role: supporting registration, liaising teams, processing certificates Requirements: Bachelor's degree in life sciences/engineering, 5+ years regulatory affairs experience (medical device preferred), international registration experience, strong oral/written communication, detail-oriented and organized. Category: Legal and Compliance Seniority: Senior Level Commitment: Full Time Workplace: Onsite Languages: English