OverviewAre you a CSV expert passionate about automation, compliance, and helping deliver life-saving medicines? Our client, a leading aseptic drug product facility, is expanding their automation project support team.ResponsibilitiesAct as the Subject Matter Expert for Computer System Validation (CSV), supporting automation projects across formulation, filling, lyophilisation, and packaging.Prepare and execute validation documentation, perform risk assessments, review vendor protocols, and ensure compliance with GxP, 21 CFR Part 11, and GAMP 5.What You’ll NeedDegree in Engineering, Computer Science, or related field5+ years of control systems validation experience in pharma/biotechExpertise with PLC/SCADA systems & OSIsoft PI validationStrong understanding of GAMP SDLC & regulatory requirementsWhy JoinCompetitive contract ratesLong-term opportunity with a leading global manufacturerBe part of a team committed to continuous improvement & innovationApplicationApply now or reach out directly: William@eu-recruit.comJob detailsSeniority level: Mid-Senior levelEmployment type: Full-timeJob function: Engineering and ManufacturingIndustries: Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Biotechnology Research
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