Sr. RA Associate Consultant
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Description
This position is listed on behalf of a partner company, who manages all applications and next steps.
Our partner is looking for a Sr.
RA Associate Consultant based in Canada.
This is a client-facing Regulatory Affairs consulting opportunity supporting medical device regulatory activities in a collaborative project environment.
You will work closely with regulatory project teams to develop, update, review, and maintain technical documentation in line with EU MDR and other applicable
requirements
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