Senior CQV Engineer (Process Equipment)

https://www.teamhorizon.ie/job-search/1155-senior-cqv-engineer-process-equipment/engineering/sligo/job2024-02-12 15:20:062051-06-28Team Horizon
Job TypeContractor
AreaSligoSligoIreland
SectorEngineering
Start Date
AdvertiserDavid Connolly
Job Ref1003163
Job Views438
Description
CQV Engineer (Process Equipment)

 

Team Horizon is seeking a CQV Engineer (Process Equipment) for a high-value expansion pharmaceutical in the North-West. In this role the CQV Engineer will be responsible for all aspects of the process equipment package, involved in the entire project lifecyle from design stage to commercial handover. 

 

Why you should apply:

·       You will join a fast-paced global engineering projects team, working in a dynamic environment.

·       Strong culture of innovation, autonomy and excellence.

·       Competitive hourly rates

 

 

What you will be doing:

·       Delivery of process systems and vendor packages

·       Working as part of a large CAPEX Projects team within a start-up GMP facility (greenfield / brownfield).

·       Involvement in design, Vendor review, FAT, SAT, I/O/PQ

·       Work with project stakeholder team to ensure all process equipment and systems are managed appropriately for the entire Project Lifecycle.

·       Perform and lead all field walk-downs for all relevant systems.

·       Ensure Commissioning readiness of all equipment and systems and to support Equipment Start-up and CQV Testing.

·       Review and approval of all Turn-Over Packages, both Vendor and Contractor within the Process Equipment Scope.

·       All other duties as requested or assigned.

 

What you need to apply:

·       7+ years’ experience of working in large-scale pharma construction projects & proven experience of process equipment vendor package owner for large construction projects

·       Great communicator and team player

·       Knowledge of risk based (ASTM E2500) approach to CQV

·       Experience of working to deadlines within a time critical environment

Working knowledge of US FDA & EU GMP regulatory requirements
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