An engineering consultancy firm in Sligo is looking for a professional to coordinate its validation program.
The ideal candidate must have a 3rd level qualification in a relevant engineering or scientific discipline, alongside 5-10 years of experience in a cGMP regulated environment.
Responsibilities include ensuring compliance of computerized systems, directing validation efforts, and generating validation plans.
This is a full-time, onsite position offering an opportunity to work with prominent life sciences and technology clients.
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