CSV / Validation Test Engineer (MES / DeltaV), Limerick

Location:

Ireland (Hybrid) Contract:

12 months Rate:

Competitive hourly rate (DOE) Overview

We'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 doing

Execute

IQ/OQ/PQ validation activities

across MES and/or DeltaV systems Perform

system testing, defect identification, and resolution support Develop and execute

validation and test scripts Work closely with QA, automation, and engineering teams Ensure systems are

inspection‑ready and fully compliant Support validation activities during

system rollout and readiness phases What we're looking for (essential)

Strong experience in

CSV / validation within pharma or biotech Proven hands‑on experience executing

IQ/OQ/PQ (not just reviewing) Experience testing

MES and/or DeltaV systems Solid understanding of

GxP / GMP requirements Comfortable working in

fast‑paced, delivery‑focused environments Nice to have

Experience with

Emerson Syncade or similar MES platforms Previous involvement in

system go‑live or pre‑production phases

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