This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME) based in Canada. Join a global clinical research environment where regulatory compliance and quality excellence contribute to the development of life-changing therapies. As a Regulatory Affairs Consultant, you will serve as a subject matter expert in controlled document management, with a focus on Veeva Quality and GxP compliance. You will play a key role in maintaining accurate, compliant, and inspection-ready documentation across regulatory and quality operations. Working closely with cross-functional teams, you will strengthen document governance, training compliance, and Quality Management System (QMS) processes. You will also support regulatory inspections, identify compliance risks, and drive continuous improvement initiatives. This fully remote opportunity offers an environment focused on collaboration, professional growth, and operational excellence within the pharmaceutical and biotechnology industries.