Principal Regulatory Affairs Specialist - Bracco Medical Technologies
Bracco(1 day ago)
About this role
The Principal Regulatory Affairs Specialist at Bracco Medical Technologies ensures that the company's medical devices meet global regulatory standards, manages submissions, interacts with regulatory authorities, and supports product compliance and lifecycle management.
Required Skills
- Regulatory Affairs
- 510(k)
- EU MDR
- FDA
- Health Canada
- Medical Devices
- Regulations
- Technical Documentation
- Submission
- International Compliance
About Bracco
bracco.comSince the kick-off in 1927, Bracco has grown to become a leading authority in improving people’s lives by shaping the future of prevention and precision imaging.
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