Senior Regulatory Affairs Specialist
Medtronic(6 days ago)
About this role
The role involves supporting design and development activities within the regulatory framework for medical devices and pharmaceuticals. It includes preparing documentation for global regulatory submissions, maintaining regulatory files, and developing regulatory strategies, working closely with various internal teams and external agencies.
Required Skills
- Regulatory Affairs
- Documentation
- Regulatory Strategy
- Medical Devices
- Pharmaceuticals
- Regulatory Submissions
- Internal Audits
- Change Control
- Regulatory Compliance
- Data Management
Qualifications
- Bachelor’s degree in Medical, Mechanical, Electric Life Science or related field
- 7+ years experience in regulatory affairs in medical device or pharmaceutical industry
About Medtronic
medtronic.comPeople-centered, data-driven, personalized. Solving our world’s biggest health challenges with advanced technology.
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