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C&Q Document Reviewer

  1. Dublin
Dublin
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
03-10-2023
32100

This vacancy has now expired

C&Q Document Reviewer - Pharmaceuticals - 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.

Your role will be focused on the documentation review and approval of Vendor Turnover Packages and Trade Turnover Packages.  These will primarily be made available for review electronically.

Responsibilities:
  • Review Turnover Packages.  Follow up issues with applicable vendor/contractor.
  • Approve documentation within Turnover Packages and fully compiled Turnover Packages.
  • Attend FAT, where onsite fabrication documentation review is required prior to uploading to electronic document system.
  • Participate in design document reviews and ensure that quality aspects are included in design.
  • 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.
  • Track and confirm closure of actions items identified through FAT, HAZOP, Design Qualification and other reviews.
  • Perform shakedown and commissioning and qualification of systems.
Requirements:
  • B.Sc/B.Eng. degree in engineering discipline, with particular emphasis mechanical or process engineering.
  • Minimum of 2 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 EIDA and/or PIMS an advantage.
If this sounds like the position for you then please apply today!

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

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