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 databasesEnsure documents remain current through regular review controlsTrack and coordinate document changes for approvalSupport document control implementation across plasma supply chain areasPerform assigned duties for the Quality System ManagerRequirements:Bachelor's degree in health-related sciencesTwo years' minimum blood, plasma, or pharmaceutical industry experienceAbility to follow, explain, and enforce SOPsExperience in change and deviation management preferredStrong integrity and commitment to quality and complianceBring document control discipline, regulatory understanding, and explicit communication to Grifols' quality management system in Winnipeg.

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