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CQV Engineer

  1. Dublin
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
26-05-2023
31429
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CQV Engineer – Life Science- Contract – Dublin

Do you want to work with an exciting company who are an established market leader within their niche field? We have a fantastic opportunity for a CQV Engineer to work on an exciting CAPEX project in Ireland on an initial 24-month contract.

CQV Engineer Responsibilities:
  • Participate in design document reviews and ensure that quality aspects are included in design.
  • Attend FAT and execution of agreed testing protocols and sign off on permission to ship forms.
  • Generate CQV documents at project level and for specific equipment/systems. Liaising with Quality, Engineering and CQV to align on Critical parameters and document content.
  • Work with the automation teams, ensure that process descriptions are provided, and Functional Specs are reviewed and approved to ensure that the automation element of the project meets schedule.
  • Partake in HAZOPs and other required process safety reviews.
  • Track and confirm closure of actions items identified through FAT, HAZOP, Design Qualification and other reviews.
  • Maintain a strong interface with the Automation and Engineering teams to ensure that the information flow meets the needs of the Automation and Engineering teams, resolving issues as they arise.
  • Participate in construction system completion walkdowns.
  • Perform shakedown and commissioning and qualification of systems.
 

About you:
  • B.Sc/B.Eng. degree in engineering discipline, with particular emphasis mechanical or process engineering.
  • Minimum of 4 years’ experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment.
  • Demonstrated ability to work on own initiative and proactively respond to business needs.
  • Excellent interpersonal and communication skills.
  • Familiar with Delta-V & Navis Works an advantage
 

Are you a good fit for a CQV Engineer? Get in touch with us today.



The candidate must have the rights to work in the location stated in the job advert.

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