Senior Regulatory Affairs Consultant – EU MDR Expert (Manitoba)

Senior Regulatory Affairs Consultant – EU MDR Expert (Manitoba)

12 Oct
|
ClinChoice
|
Manitoba

12 Oct

ClinChoice

Manitoba

ClinChoice Canada Inc. is seeking a Sr. Regulatory Affairs Associate – CONSULTANT to join its global CRO team on a 12‑month contract.
You will work closely with regulatory project teams to review, draft, and manage Technical Documents for EU MDR and other regulatory needs, ensuring accuracy and timely delivery. The role requires at least 2 years in Regulatory Affairs focused on EU MDR, knowledge of ISO13485 and FDA regulations, and robust English communication.

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📌 Senior Regulatory Affairs Consultant – EU MDR Expert (Manitoba)
🏢 ClinChoice
📍 Manitoba

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