Remote Senior Regulatory Affairs Specialist; Devices
Siemens Healthineers Canada is seeking a Senior Regulatory Affairs Specialist to lead submissions for FDA 510(k), IVDR, and other regulatory activities. This remote role supports cross‑functional teams and quality systems, ensuring compliant lifecycle documentation.
The ideal candidate has 4+ years in IVDs or medical devices, GMP experience, and strong communication skills. You will train stakeholders, review labeling, and prepare technical files while staying audit‑ready in a dynamic healthtech
We have an opening for a Remote Senior Regulatory Affairs Specialist (Devices) in Ottawa, ON, Canada within Legal, Management & Operations.
The Remote Senior Regulatory Affairs Specialist (Devices) role at Siemens Healthineers is now open for applications in Ottawa, ON, Canada.
Join us at Siemens Healthineers as our next Remote Senior Regulatory Affairs Specialist (Devices) in Ottawa, ON, Canada.
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