About the role
CSV Engineer - Galway - 6 Month Contract Are you looking for the opportunity to work alongside a global pharmaceutical organisation in Galway? Our esteemed client is looking for a CSV Engineer to join their team in their existing manufacturing facility in Galway.
The facility is a responsible for tablet manufacturing (OSD) and secondary packaging (blister packing and bottle primarily for tablets and capsules), and our client is looking for a CSV Engineer to help maintain manufacturing operations.
What You'll Need
- Lead CSV activities across GxP systems, including preparation and execution of validation deliverables (URS, RA, IQ/OQ/PQ, reports).
- Maintain the validated state of computerised systems and perform periodic reviews to ensure ongoing compliance.
- Manage QMS records including Change Controls, Deviations, Investigations, and CAPAs.
- Support audit readiness by ensuring documentation accuracy and participating in internal/external inspections.
What you'll do:
- Extensive experience in Computer System Validation within a GxP-regulated environment.
- Strong knowledge of GAMP 5, data integrity principles, Annex 11, and 21 CFR Part 11.
- Proven experience delivering full CSV lifecycle documentation and managing QMS processes.
- Excellent communication skills and ability to work autonomously in a compliance-driven environment.
If this role is of interest to you, please apply now!
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