Grifols Plasma Center Validation Specialist

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

• 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