A leading pharmaceutical manufacturer in Dublin is seeking a CQV Engineer to lead the commissioning and qualification lifecycle supporting CAPEX projects. The ideal candidate will have at least 5 years of experience in a pharmaceutical manufacturing setting, focusing on OSD process equipment and technical documentation for GMP compliance. You will be responsible for ensuring all processes align with strict cGMP standards while fostering a culture of quality across engineering projects. The role offers a full-time position with a 12-month contract starting March 2025.
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