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 strong 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 in Mississauga employer: Grifols, S.A
Grifols is an exceptional employer that fosters a collaborative and innovative work culture, dedicated to improving healthcare globally. Located in Toronto, Ontario, the company offers competitive benefits, professional development opportunities, and a commitment to employee growth, making it an ideal place for those passionate about making a meaningful impact in the healthcare sector.
