Regulatory Affairs Specialist
Stryker(1 day ago)
About this role
A Regulatory Affairs Specialist with approximately 3 years of experience supports regulatory activities throughout the product lifecycle, ensuring compliance with various regulations, assisting with submissions, and collaborating with cross-functional teams to maintain regulatory standards in the medical device industry.
Required Skills
- Regulatory Affairs
- Regulatory Submissions
- Medical Devices
- ISO 13485
- FDA
- CE Marking
- MDSAP
- Quality Assurance
- Regulatory Compliance
- Global Strategy
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