GMP documentation control is central to this Specialist role at Grifols in Winnipeg, supporting accurate, compliant quality records and tracking systems.
Reporting to the Quality Management System Manager, the Documentation Specialist supports QA document processing, filing, tracking, and archiving. You will maintain controlled documents, monitor activities affecting product quality, and support the quality management system. The work covers SOPs, forms, protocols, reports, and plasma supply chain documentation.
Key Responsibilities: Maintain GMP templates and document tracking systems
Coordinate change control requests, approvals, preparation, and distribution
Review Documentation Lifecycle System SOPs against Canadian requirements




Compile Quality System key process indicator information
Prepare Grifols viral marker data for PPTA reporting
Requirements: Bachelor’s degree in health-related sciences
Minimum two years’ blood, plasma, or pharmaceutical experience
Understanding of quality management systems and related regulations
Knowledge of Health Canada, FDA, and EMA GMP regulations
Microsoft Office Suite proficiency and robust communication skills
Apply documentation control, change management, and GMP knowledge to strengthen Grifols quality operations in Winnipeg.

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📌 GMP Documentation Control Specialist (Ontario)
🏢 Grifols
📍 Ontario