Veeva Quality expertise defines this fully remote Regulatory Affairs Consultant opportunity in Canada, focused on controlled documents and GxP compliance. Support inspection-ready quality operations.
This consultant serves as a subject matter expert in Veeva Quality and electronic document management systems. The work covers document governance, training compliance, Quality Management System processes, and regulatory inspections. Collaboration spans Regulatory Affairs, Quality, CMC, Clinical Operations, Pharmacovigilance, and Medical Writing teams.
Key Responsibilities: Oversee controlled document creation, review, approval, and archival
Support global GxP compliance and mitigation strategies
Prepare regulatory inspections involving FDA, EMA, and MHRA




Manage role-based GxP training governance and completion monitoring
Improve QMS workflows, templates, and governance practices
Requirements: Bachelor's degree in a related scientific or technical field
At least eight years in regulatory, quality, or GxP functions
Hands-on Veeva Vault or comparable eDMS experience
Robust FDA, EMA, ICH, and global GxP knowledge
Experience supporting inspections, audits, and compliance findings
Apply controlled document management, Veeva Quality knowledge, and GxP expertise to strengthen compliant pharmaceutical operations across Canada.

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📌 Regulatory Affairs Veeva Quality Consultant (Manitoba)
🏢 Jobgether
📍 Manitoba