A biopharmaceutical company in Carlow is seeking a Validation Engineer to support validation activities within a cGMP regulated environment.
The ideal candidate will design and execute qualification documentation, troubleshoot technical issues and collaborate with cross-functional teams to ensure compliance with regulatory standards.
Candidates should have a degree in a relevant field and experience in validation documentation and change control processes, with a familiarity in systems like DeltaV being advantageous.
This role offers the chance to contribute to continuous improvement initiatives and regulatory submissions.
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