Quality systems expertise defines this Documentation Specialist opportunity with Grifols, based in Winnipeg and focused on controlled records and compliance.
The role provides QA support for GMP documentation processing, filing, tracking, and archiving. Reporting to the Quality Management System Manager, you will maintain the document control system and QA operations files. Your work supports accuracy, integrity, availability, and legibility across controlled documentation affecting plasma operations and product quality.
Key Responsibilities: Maintain controlled documents, templates, and tracking databases
Ensure documents remain current through regular review controls
Track and coordinate document changes for approval




Support document control implementation across plasma supply chain areas
Perform assigned duties for the Quality System Manager
Requirements: Bachelor’s degree in health-related sciences
Two years’ minimum blood, plasma, or pharmaceutical industry experience
Ability to follow, explain, and enforce SOPs
Experience in change and deviation management preferred
Solid integrity and commitment to quality and compliance
Bring document control discipline, regulatory understanding, and clear communication to Grifols’ quality management system in Winnipeg.

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📌 Quality Systems Documentation Specialist (Ontario)
🏢 Grifols
📍 Ontario