Regulatory Affairs Specialist: Medical Devices

Fuze Health Inc. in Dublin seeks a Regulatory Affairs Specialist to support regulatory requirements across global jurisdictions for in vitro diagnostics and medical devices.

You will collaborate with clinical, quality, and engineering teams to prepare submissions, maintain EU IVDR/MDR files, and support post-market activities. The role emphasizes cross-functional teamwork, continuous improvement, and building relationships with regulatory authorities, consultants, and internal departments to