Lead GMP audit strategy and supplier qualification as Grifols’ Supply and Audit Director, supporting regulatory compliance across Canadian Plasma activities.
Reporting to the Quality Senior Director, this director provides Quality Assurance leadership for risk-based audits, supplier performance, and regulatory inspections. The position assesses GMP risks, quality trends, and quality-system effectiveness across Grifols Canada Plasma. It also supports quality agreements, auditor development, and continued supplier qualification within a matrix organization.
Key Responsibilities: Develop and oversee global risk-based GMP audit programs
Participate in internal and external GMP audits
Lead auditor and supplier-qualification training programs
Support regulatory inspections and notified-body audits




Maintain quality agreements with critical suppliers
Requirements: Bachelor’s degree in health-related sciences, preferably Pharmacy
Post-graduate certification in Quality Management
Auditor certification and pharmaceutical GMP auditing experience
Ten years’ general experience, including six auditing years
Microsoft Office proficiency and robust analytical communication skills
Apply your GMP auditing, supplier oversight, and Quality Assurance leadership experience to Grifols Canada Plasma’s regulated operations.

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📌 Supply and Audit Director (Ontario)
🏢 Grifols
📍 Ontario