C&Q Engineer - Ireland, Dublin - 12 Months Contract
With more than 2,000 employees, more than 300 million units per year, and a lot of innovative medicines in the pipeline, our client is one of the largest production units in the world.
The company produces, packs and distributes in a high-tech, sterile injectable medicines environment.
More than 1 million injectable medicines are produced, packaged and distributed every day to 170 countries worldwide.
Do you want to work with an exciting company that is an established market leader within its 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.
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.
Liaise with Quality, Engineering and CQV to align on Critical parameters and document content.
Track and confirm closure of action items identified through FAT, HAZOP, Design Qualification and other reviews.
Maintain a strong interface with the Automation and Engineering teams to ensure that information flow meets their needs and resolve issues as they arise.
Participate in construction system completion walkdowns.
Perform shakedown, commissioning and qualification of systems.
Desirable Experience / Qualifications
B.Sc/B.Eng.
degree in engineering discipline, with emphasis on 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 & NavisWorks is an advantage.
If this role is of interest to you, please apply now!
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