A prominent recruitment agency is seeking a qualified Inspection C&Q Engineer for a biopharmaceutical client in Dublin. This full-time role involves developing CQV testing documentation, ensuring compliance with GMP, and managing risks associated with Inspection Systems in the sterile drug product facility. The ideal candidate will have a BS degree in a scientific or engineering field and a minimum of 5 years' experience in the pharmaceutical industry, with a strong collaborative spirit and excellent communication skills.
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