Regulatory Affairs Specialist - Neuro
Medtronic(11 days ago)
About this role
A Regulatory Affairs Specialist at Medtronic supports the development and submission of regulatory documentation for medical devices across global markets. The role involves collaboration with teams, ensuring compliance, and maintaining product registrations, focusing on innovative healthcare solutions.
Required Skills
- Regulatory Submissions
- Medical Devices
- FDA
- EU MDR
- ISO 13485
- ISO 14971
- Quality Standards
- Regulatory Requirements
- Communication
- Organizational Skills
About Medtronic
medtronic.comPeople-centered, data-driven, personalized. Solving our world’s biggest health challenges with advanced technology.
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