A leading pharmaceutical organization in Ireland seeks a Validation Specialist for a hybrid role focusing on testing and validation of manufacturing systems. The successful candidate will execute IQ/OQ/PQ validation and work closely with QA, automation, and engineering teams to ensure systems are compliant and ready for production. Essential qualifications include experience in CSV within pharma or biotech, hands-on IQ/OQ/PQ execution, and understanding of GxP/GMP requirements. Experience with Emerson Syncade is a plus.
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