Partner Company in Canada is seeking a Sr. RA Associate Consultant to support regulatory activities for medical devices. You will work with client-facing teams to develop, review, and maintain technical documentation in line with EU MDR and other applicable regulations.
This 12-month contract offers exposure to global regulatory work, collaboration with cross-functional stakeholders, and prospects to advance regulatory submissions and quality control processes.
📌 Senior Regulatory Affairs Consultant – Remote Canada Quebec City
🏢 Jobgether
📍 Quebec City
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.