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C&Q Engineer

  1. Ireland, Dublin
Dublin
  1. Contract
Competitive
  1. Compliance / Quality Assurance
37261
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C&Q Engineer - Ireland, Dublin - 12 Month Contract

With more than 2,000 employees, more than 300 million units per year, and a lot of innovative medicines in the pipeline, no wonder our client is one of the largest production units in the world! Our client produces, packs and distributes in a high-tech environment, sterile injectable medicines. More than 1 million injectable medicines are produced, packaged and distributed every day. Their destination: 170 countries, worldwide! 

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 C&Q Engineer to work on an exciting CapEx project in Dublin on an initial 12 month contract. As a C&Q Engineer you will play a key role in the successful delivery of a new state of the art facility.

Essential Duties and Responsibilities for this C&Q Engineer role include, but are not limited to, the following:
  • 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.
  • 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.
Desirable Experience:
  • B.Sc/B.Eng. degree in engineering discipline, with particular emphasis mechanical or process engineering.
  • Extensive 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
  • Extensive Clean in Place (CIP) experience
If this role is of interest to you, please apply now!
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