Validation Engineer - cGMP & Process Excellence

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.