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 environment, 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
- Robust 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