Location: Ireland (Hybrid)Contract: 12 monthsRate: Competitive hourly rate (DOE)OverviewWe're supporting a global pharmaceutical organisation during a critical phase of manufacturing systems readiness, with a focus on validation and testing across MES and automation platforms.This role is centred on hands‑on testing and validation execution, (not QA oversight/documentation‑only work). You'll be working within a delivery‑focused environment to ensure systems are fully tested, compliant, and ready for use in a regulated production setting.What you'll be doingExecute IQ/OQ/PQ validation activities across MES and/or DeltaV systemsPerform system testing, defect identification, and resolution supportDevelop and execute validation and test scriptsWork closely with QA, automation, and engineering teamsEnsure systems are inspection‑ready and fully compliantSupport validation activities during system rollout and readiness phasesWhat we're looking for (essential)Strong experience in CSV / validation within pharma or biotechProven hands‑on experience executing IQ/OQ/PQ (not just reviewing)Experience testing MES and/or DeltaV systemsSolid understanding of GxP / GMP requirementsComfortable working in fast‑paced, delivery‑focused environmentsNice to haveExperience with Emerson Syncade or similar MES platformsPrevious involvement in system go‑live or pre‑production phases
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