Sr. RA Associate Consultant

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.

The role combines regulatory knowledge with detailed document management, quality control, and cross-functional coordination. You will help ensure regulatory submissions and supporting documentation are accurate, complete, current, and compliant.

The position requires strong independence, organization, and communication skills, while maintaining close collaboration with regulatory experts, local affiliates, and project stakeholders. This 12-month contract, with potential for extension, offers meaningful exposure to global medical device regulatory work and a trusted client-facing environment.