A leading pharmaceutical company is seeking a Validation Engineer to join its Technical Operations team in Sligo.
This role offers the candidate the chance to manage validation activities while ensuring compliance with regulatory standards.
Responsibilities include co-ordinating the Validation Program, managing validation plans, and ensuring that all systems meet necessary standards.
Candidates should have a relevant engineering degree and at least 2 years of experience in a cGMP environment.
Excellent communication and problem-solving skills are required.
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