Clin Choice 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 ISO
13485 and FDA regulations, and strong English communication.
Join us at Clin Choice as our next Senior Regulatory Affairs Consultant – EU MDR Expert in Canada.
We are looking to fill the Senior Regulatory Affairs Consultant – EU MDR Expert position at Clin Choice in Canada.
The Senior Regulatory Affairs Consultant – EU MDR Expert role at Clin Choice is now open for applications in Canada.
We are currently recruiting a Senior Regulatory Affairs Consultant – EU MDR Expert for our team in Canada.
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