A leading biopharmaceutical company in Carlow seeks an Engineering Specialist (Validation) to enhance compliance and validation processes in a c GMP environment.
The ideal candidate will possess a relevant technical qualification and experience in GMP settings, with skills in documentation, project delivery, and regulatory compliance.
Excellent communication and analytical skills are required, and the role supports flexible hybrid working arrangements.
The position includes responsibilities in validation documentation, quality engagement, and compliance auditing.
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