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 workplace, 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
• Strong 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.
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📌 Grifols Plasma Center Validation Specialist (Toronto)
🏢 Grifols
📍 Toronto