Join Grifols to ensure compliance and quality as a Validation Specialist for Plasma Centers. The role requires travel for conducting validation tests while maintaining adherence to industry standards. As a Field Validation Specialist, you will help uphold Grifols' commitment to quality in plasma-derived medicines.

With at least two years of experience in a cGMP setting, you will interact with staff to facilitate validation processes. Your expertise will ensure timely approvals prior to routine use of systems. Key Responsibilities:
Conduct and document validation testing at donor centers
Assist in the evaluation of validation methodologies and systems
Communicate compliance concerns to quality teams
Prepare and distribute validation reports
Train donor center staff on validation activities Requirements:
2+ years experience in quality assurance, particularly in cGMP
Solid critical thinking and problem-solving abilities
Familiarity with Microsoft Office and laboratory equipment
Ability to communicate complex information clearly
Flexibility for extensive travel across Canada Contribute to better healthcare outcomes by leveraging your validation skills at Grifols.

📌 Grifols Plasma Center Validation Specialist Toronto
🏢 Grifols
📍 Toronto