Lead GMP audits and supplier qualification for Grifols Canada Plasma in Winnipeg, applying quality assurance expertise within a regulated healthcare organization.
As Supply and Audit Director, you will lead risk-based audit programs, auditor development, and supplier oversight. The position reports to the Quality Senior Director and supports regulatory inspections. Your work covers Canadian regulations, cGMP requirements, FDA standards, and European standards across Grifols Canada Plasma activities.

Key Responsibilities
Develop and oversee global risk-based GMP audit programsParticipate in internal and external GMP auditsLead auditor and supplier qualification training programsProvide feedback on findings, risks,



and corrective actionsSupport regulatory inspections and notified body auditsRequirements: Bachelor’s degree in health-related sciences, preferably PharmacyPost-graduate certification in Quality ManagementAuditor certification and pharmaceutical GMP auditing experienceTen years’ general experience, including six GMP audit yearsMicrosoft Office proficiency and robust communication skillsBring GMP auditing, supplier qualification, and regulatory inspection expertise to Grifols Canada Plasma’s quality assurance leadership in Winnipeg. #J-18808-Ljbffr

📌 Supply And Audit Director Gmp (Winnipeg)
🏢 Grifols
📍 Winnipeg