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Regulatory Affairs Specialist: Accelerate Device Approvals
Posted 7 days 21 hours ago by Stryker Group
Permanent
Full Time
Other
Cork, Cork, Ireland
Job Description
Stryker Ireland is seeking a Regulatory Affairs Specialist to support bringing medical devices to market and maintaining ongoing regulatory compliance. You will work under supervision and collaborate with cross-functional teams to develop global regulatory strategies, author submissions, and interact with regulators.
The role focuses on US, EU, and international regulatory requirements, including labeling review and change assessment, with opportunities to contribute to post-market activities
