Are you a Commissioning & Qualification (C&Q) Engineer with a passion for ensuring GMP compliance, safety, and efficiency in pharmaceutical/biotech projects? Were looking for a driven professional to lead C&Q activities for clean utilities, facilities, and process equipment in a high-impact capital project ?? Key Responsibilities: ? Own C&Q projectsdrafting protocols, executing tests (FAT/SAT/IV/FT), and ensuring compliance.
? Generate critical C&Q documentation (Plans, Summary Reports, URS, Risk Assessments).
? Supervise & coordinate C&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 within Pharma/Biotech.
??Technical degree in Engineering (or equivalent).
?? Strong knowledge of GMP, 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