13 Oct
|
ClinChoice
|
Winnipeg
13 Oct
ClinChoice
Winnipeg
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 (Winnipeg)
🏢 ClinChoice
📍 Winnipeg