GMP Validation Engineer - Isolator & Sterility Systems

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Ireland

Ireland

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À propos

A leading biotechnology firm in Leinster is seeking an Engineering Specialist (Validation) to support validation activities in a cGMP regulatory environment.
Ensure you read the information regarding this opportunity thoroughly before making an application.
Key responsibilities include authoring and executing validation documentation, resolving technical issues, and ensuring compliance with regulatory requirements. xcfaprz
The ideal candidate will have significant experience in GMP environments and relevant qualifications in pharmaceutical sciences, bringing strong analytical skills to the team.
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Ireland

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