A leading biopharmaceutical company in Munster, Ireland is seeking a professional to lead the execution of cleaning validation protocols and support commissioning activities in a state-of-the-art aseptic manufacturing site. The ideal candidate should possess a degree in Engineering, Chemistry, or related discipline and have over 3 years of cleaning validation experience within GMP environments. This role involves working cross-functionally with various teams during the facility's start-up phase.
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