Brilliant opportunity for an experienced CQV Engineer to join a world leading biopharma facility based in Carlow. This role will involve supporting all suite teams during a commissioning and qualification program for a new facility build! You will assist the C&Q Technical Lead in the planning and tracking of activities.
As part of this project you will be responsible for implementing C&Q strategies as set out by the C&Q Lead EMEA ensuring that system delivery progresses in accordance with the approved project schedule.
Excellent remenuration on offer with flexible working options and the opportunity to work one of the most exciting projects in the industry.
You should have a bachelor of Engineering or Science Degree in Engineering with a minimum of 5 years’ experience in commissioning and/or validation of USP/DSP/Facilities/Utilities systems within Pharmaceutical industry.
Send your CV now if you're interested in taking the next step in your career!
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