Sr Regulatory Affairs Spec -Neuro
Medtronic(7 days ago)
About this role
Medtronic is seeking a Senior Regulatory Affairs Specialist to develop strategies for worldwide product registration, prepare submissions, and ensure compliance with global regulatory requirements. The role involves collaborating with cross-functional teams, interacting with regulatory agencies, and supporting both new and existing products in a regulated medical device environment.
Required Skills
- Regulatory Submissions
- FDA
- EU MDR
- QMS Audits
- Post-Market Surveillance
- ISO 13485
- ISO 14971
- Medical Devices
- Device Registration
- Regulatory Compliance
About Medtronic
medtronic.comPeople-centered, data-driven, personalized. Solving our world’s biggest health challenges with advanced technology.
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