Clean Utilities C&Q Engineer
Duration
Option 1: February 2026 – December 2026
Option 2: February 2026 – May 2027
Location:
Cruiserath, Ireland
Working hours:
39 hours per week
Onsite requirements:
Onsite role
Engagement Type:
LTD Company Contractors ONLY
Hourly Rate:
€70–€80 per hour (depending on experience)
LEGAL RIGHT TO WORK:
You must have the legal right to work in Ireland. No sponsorship can be provided.
Atrium Global is supporting a client in the pharmaceutical industry to appoint Clean Utilities C&Q Engineers to join a critical sterile drug product facility project.
Job Overview
Working alongside the CQV Lead, you will prepare and execute commissioning and validation testing for clean utility systems at the Cruiserath Drug Product Facility. You will ensure compliance with GMP, regulatory standards, and project schedules while delivering high quality documentation and execution.
RESPONSIBILITIES
* Develop and execute CQV testing documentation for Clean Utilities across a sterile drug product facility
* Deliver assigned tasks to meet safety, CQV schedule and documentation quality targets
* Ensure GMP equipment and Clean Utilities are tested in line with EU and FDA regulations and company standards
* Ensure commissioning testing aligns with required project standards
* Manage deviations related to assigned equipment and utilities
* Identify and categorise CQV risks, producing mitigation action plans
* Execute FAT activities and leverage results into the qualification lifecycle
* Complete all assigned training within agreed timelines
REQUIREMENTS
* Proven experience executing CQV testing from initiation through to completion
* Full CQV project lifecycle expertise from design through to handover
* Experience delivering tasks as part of a diverse team within budget and schedule
* CQV experience with sterile manufacturing equipment and integrated automation
* Strong knowledge of High Purity Water systems (PW & WFI), Clean Steam, and High Purity Gas systems
* Strong documentation, execution and planning skills with on time performance record
* Excellent communication skills and ability to influence collaboratively
* Experience working within matrix environments
* Experience with electronic validation platforms such as ValGenesis or Kneat
* Degree in a scientific, engineering or technical discipline
* Minimum 5 years pharmaceutical industry experience, ideally with sterile filling line experience