A leading biopharma company located in Stamullen is seeking a Validation Specialist for a permanent role. This position involves implementing and executing validation tasks related to processes, facilities, and equipment development. The ideal candidate should have a degree in Quality/Validation, a minimum of 2 years of relevant experience, and proficiency in Microsoft Office. This is a full-time, on-site role, requiring strict adherence to regulatory standards and strong problem-solving skills.
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