A global biopharmaceutical organization is seeking an experienced CSV Engineer for their new greenfield manufacturing facility in Ireland. The ideal candidate will lead Computer System Validation activities for QC laboratory systems, ensuring compliance with GMP standards. This role involves developing validation documentation and collaborating with cross-functional teams. A degree in Engineering or Computer Science and proven experience in CSV within pharmaceutical or biotech environments are essential. This opportunity offers the chance to contribute to a cutting-edge project.
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