Grifols is seeking a Validation Specialist to ensure that the company adheres to Good Manufacturing Practices (cGMP) and FDA standards throughout the evaluation, review, and approval of documentation. The role involves developing validation procedures, investigating deviations, and ensuring compliance with SOPs. The position is hybrid, based in RTP, NC.
Requirements
- Bachelor's degree
- 2+ years of quality and validation experience in a cGMP and/or IT environment
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Requirements: Bachelor's degree required. 2+ years' cGMP experience. Excellent communication & analytical skills