CQV Engineer

https://www.teamhorizon.ie/job-search/1820-cqv-engineer/engineering/roscommon/job2026-07-16 12:23:372053-11-29Team Horizon
Job TypeContractor
AreaRoscommon, IrelandWestmeath, IrelandRoscommonIreland
SectorEngineering
Start Date
AdvertiserDavid Connolly
Job Ref1003964
Job Views6
Description

Team Horizon is seeking a CQV Engineer for a leading pharmaceutical company in Athlone.


We are seeking an experienced CQV Engineer to manage commissioning and qualification activities for utilities, equipment, and process systems. It’s a short term contract role


 


Why you should apply:



  • Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.

  • You enjoy working on exciting projects and want to work with a global manufacturing site in Athlone.


 


 


What you will be doing:



  • Lead the CQV strategy for the facility upgrades, ensuring alignment with project goals and regulatory requirements.

  • Develop and maintain the CQV master plan, protocols, and schedules.

  • Coordinate cross-functional teams including engineering, quality, manufacturing, IT, automation and project management.

  • Manage commissioning and qualification activities for utilities, equipment, and process systems.

  • Ensure timely execution of IQ/OQ/PQ protocols and documentation.

  • Drive resolution of CQV issues, deviations, and change controls.

  • Ensure adherence to GMP, FDA, EMA, and other applicable regulatory standards.

  • Maintain accurate and audit-ready CQV documentation.

  • Support regulatory inspections and internal audits.

  • Act as the primary CQV point of contact for project stakeholders.

  • Provide regular updates on CQV progress, risks, and mitigation strategies.

  • Collaborate with vendors and contractors to ensure CQV deliverables are met.

  • Any duties as assigned.


 


What you need to apply:



  • Bachelor’s or Master’s degree in Engineering (Mechanical, Chemical, Biopharmaceutical, or related field).

  • Minimum 5 years of experience in C&Q within the Life Sciences industry.

  • Strong knowledge of regulatory guidelines (FDA, EMA, ISPE, GAMP).

  • Hands-on experience with risk-based qualification and C&Q protocols.

  • Strong problem-solving, communication, and teamwork skills. Experience working on large-scale capital projects is a plus.

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