Benefits Package, including (but not limited to):
Competitive pension scheme
Comprehensive health and dental insurance
22 days of annual leave
Flexible time banking / overtime options
Additional competitive benefits
Job Summary
We’re thrilled to announce that our valuable Client in the Life Science sector is currently looking for a Senior CQV Utilities Engineer to join their team and be part of pharmaceutical projects in county Tipperary and the Netherlands. Permanent and Fixed-term Contract options are available for discussion
They are seeking a Senior CQV Utilities Engineer to lead the Commissioning, Qualification, and Validation (CQV) of critical utility systems in our pharmaceutical facility. This is a hands‑on, technical role with a focus on ensuring all utilities are installed, operated, and validated to meet GMP and regulatory standards. The ideal candidate will have strong experience in commissioning and qualifications of pharmaceutical utility systems and the ability to work independently or as part of a multidisciplinary team.
Key Responsibilities
Design, operate, and maintain utility systems (HVAC, WFI, purified water, cleaning steam, compressed gases, cooling towers).
Perform system validation and support IQ/OQ/PQ activities using e‑validation system.
Ensure compliance with GMP, regulatory standards, and internal quality policies.
Monitor performance, troubleshoot issues, and implement improvements.
Collaborate with production, quality, and engineering teams to ensure seamless operations.
Support audits and regulatory inspections.
Qualifications
4+ years of relevant experience in pharmaceutical utilities.
Proven CQV experience with clean and black utilities, including PW, WFI, clean steam, HVAC, process gases, and cooling towers.
Familiarity with Kneat (e‑validation system) is a bonus – training will be provided.
Knowledge of GMP, regulatory requirements, and validation protocols.
Ability to work independently in a project‑driven environment.
Strong problem‑solving, teamwork, and communication skills.
Other Requirements
Must be able to commit to a minimum 40-hour work week, with flexibility based on project needs.
This is a site‑based role.
Eligible to work in the EU without the need for visa sponsorship, now or in the future.
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