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. #J-18808-Ljbffr