Siemens Healthineers in Canada is seeking a Senior Regulatory Affairs Specialist to lead regulatory submissions and maintain lifecycle documentation for medical devices and IVDs. You will collaborate with cross‑functional teams, provide guidance on design controls, and ensure audit-ready documentation while supporting internal training and regulatory projects.
The role requires a Bachelor’s degree in a scientific discipline, 4+ years of regulatory experience, GMP exposure, and solid attention
📌 Remote Senior Regulatory Affairs Specialist - Medical Devices (Toronto)
🏢 460w EPOCAL
📍 Toronto
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