Company: Getinge
Location: Wayne, NJ, United States
Type: Full-time | Regulatory Affairs
About the Role
Getinge is hiring a Senior Regulatory Affairs Specialist to support the medical device regulatory strategy for their product portfolio across US and global markets.
Requirements
- 5+ years of regulatory affairs experience in medical devices
- Experience with FDA 510(k) and PMA submissions
- Knowledge of ISO 13485 and EU MDR
Apply: View on LinkedIn