Veeva Quality expertise defines this fully remote Regulatory Affairs Consultant prospect 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 archivalSupport global GxP compliance and mitigation strategiesPrepare regulatory inspections involving FDA, EMA,



and MHRAManage role-based GxP training governance and completion monitoringImprove QMS workflows, templates, and governance practicesRequirements:
Bachelor's degree in a related scientific or technical fieldAt least eight years in regulatory, quality, or GxP functionsHands-on Veeva Vault or comparable eDMS experienceStrong FDA, EMA, ICH, and global GxP knowledgeExperience supporting inspections, audits, and compliance findingsApply 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 Winnipeg (Canada)
🏢 Jobgether
📍 Canada