Veeva Quality expertise defines this fully remote Regulatory Affairs Consultant chance in Canada, focused on controlled documents and Gx P 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 Gx P compliance and mitigation strategiesPrepare regulatory inspections involving FDA, EMA,



and MHRAManage role-based Gx P 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 Gx P functionsHands-on Veeva Vault or comparable e DMS experienceStrong FDA, EMA, ICH, and global Gx P knowledgeExperience supporting inspections, audits, and compliance findingsApply controlled document management, Veeva Quality knowledge, and Gx P expertise to strengthen compliant pharmaceutical operations across Canada.#J-18808-Ljbffr

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