Lead Regulatory Affairs Specialist Medical Devices (m/f/d)
Novanta Inc.Berlin, Germany
Posted March 3, 2026
Full Time
About the Company
Novanta is a global team that creates engineered components and sub-systems for mission-critical applications in healthcare and advanced manufacturing.
Job Description
Lead Regulatory Affairs Specialist ensures medical devices meet regulatory requirements and coordinates regulatory submissions and approvals.
Requirements
- 5-8 years of experience in Regulatory Affairs for Medical Devices
- Completed studies in natural sciences, engineering, medical or comparable field
- Advanced training in "Manager Regulatory Affairs for Medical Devices"
- Excellent communication and team collaboration skills
- Quality-oriented, reliable, and dependable
Benefits
- Benefits not specified