About this role
Lead Regulatory Affairs Specialist Medical Devices (m/f/d) at Novanta. Location: Berlin, Berlin, Germany. Role: Managing documentation, Reviewing documentation, Supporting design controls Requirements: Extensive regulatory experience (5-8 years) in medical devices; advanced training in Regulatory Affairs; strong English (C1) and German (B2); capable of coordinating cross-functional teams. Category: Legal and Compliance Seniority: Mid Level Commitment: Full Time Workplace: Onsite Languages: English, German