Principal Regulatory Affairs Specialist
Bracco(1 month ago)
About this role
A Principal Regulatory Affairs Specialist at Bracco Medical Technologies leads regulatory strategy and supports product approvals and registrations across U.S. and international markets. This role partners with internal stakeholders and external consultants to ensure compliance with applicable regulations and maintain regulatory documentation and registrations.
Required Skills
- Regulatory Strategy
- 510(k)
- EU MDR
- Licensing Submissions
- Global Registrations
- Project Management
- FDA Interactions
- Audits
- Labeling Review
- Documentation
+2 more
Qualifications
- Bachelor’s Degree
- RAC Certification
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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