Are you aCommissioning & Qualification (C&Q) Engineer with a passion for ensuringGMP compliance, safety, and efficiency in pharmaceutical / biotech projects? Were looking for a driven professional to leadC&Q activities for clean utilities, facilities, and process equipment in a high-impact capital project! ?? Key Responsibilities : ? OwnC&Q projectsdrafting protocols, executing tests (FAT / SAT / IV / FT), and ensuring compliance. ? Generate criticalC&Q documentation (Plans, Summary Reports, URS, Risk Assessments). ? Supervise & coordinateC&Q activities, ensuring schedule adherence and risk mitigation. ? Leaddaily C&Q meetings, track progress, and report on system readiness. ? Ensuresafe startup of equipment / utilities while collaborating with cross-functional teams. ?? What You Bring : ??3+ years in Engineering or C&Q withinPharma / Biotech. ??Technical degree in Engineering (or equivalent). ?? Strong knowledge ofGMP, regulatory requirements, and risk-based qualification. ?? Leadership & communication skills to engagesenior stakeholders. ?? Experience withpaperless validation systems is a plus! Skills : Clean Utilities Process Equipment GMP Pharma Kneat
Engineer • Dublin, Leinster, Republic of Ireland