Regulatory Affairs Specialist
Medtronic(20 days ago)
About this role
A Regulatory Affairs Specialist at Medtronic supports global product registration and regulatory compliance for medical devices, with emphasis on markets in the Americas and the EU. The role sits within the company’s regulatory organization and contributes to enabling product market entry while ensuring adherence to global regulatory and quality standards.
Required Skills
- Regulatory Submissions
- Regulatory Strategy
- FDA Submissions
- EU MDR
- ISO 14971
- ISO 13485
- Communication
- Negotiation
- Project Management
- Quality Management
+1 more
Qualifications
- Bachelor’s Degree in Scientific Discipline
- Advanced Degree in Scientific Discipline
About Medtronic
medtronic.comPeople-centered, data-driven, personalized. Solving our world’s biggest health challenges with advanced technology.
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