A leading life sciences consulting firm is seeking a CSV engineer for their Tipperary location.
The candidate will be responsible for Computer System Validation ensuring compliance with regulatory standards.
Key responsibilities include developing quality documents, ensuring vendor compliance, and working closely with automation teams.
The ideal candidate will have a minimum of 3 years' experience in pharmaceutical manufacturing and expert knowledge of GAMP5.
Proficiency in Emerson DeltaV and strong communication skills are essential.
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