Sr Regulatory Affairs Spec
Medtronic(10 days ago)
About this role
This role supports international registrations for Medtronic's Acute Care & Monitoring products, overseeing regulatory submission documentation, licensing, and compliance strategies. The position involves liaising with regulatory agencies and optimizing tracking systems to facilitate clinical trial approvals and product registrations.
Required Skills
- Regulatory Submissions
- Documentation
- Clinical Trials
- Regulatory Compliance
- Labeling
- Manufacturing Support
- Global Regulations
- Audits and Inspections
- Registration Strategies
About Medtronic
medtronic.comPeople-centered, data-driven, personalized. Solving our world’s biggest health challenges with advanced technology.
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