C&Q Engineers
QCS StaffingIreland1 day ago
ContractEngineering, Information Technology
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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 C&Q Engineer you will play a key role in the successful delivery of a new state of the art facility.
What You'll Do
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 C&Q Engineer you will play a key role in the successful delivery of a new state of the art facility.
What You'll Do
- 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.
- 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.
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