Hybrid Regulatory Affairs Specialist - Medical Devices

Stryker Ireland is seeking a Regulatory Affairs Specialist to contribute to global regulatory strategies and submissions for medical devices. You will interact with regulatory bodies, review labeling, and ensure compliance across US, EU, and other regions while working under supervision.

The role emphasizes collaboration with global affiliates, participation in development teams, and ongoing regulatory support for launched products and changes. Hybrid work flexibility is offered in Ireland.