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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