C&Q Engineer – GMP Projects

pb5–6-month assignment | French and English required |Equipment, Utilities and CSV /b /ppHelp deliver pharmaceutical capital projects from construction through qualification. In this on-site assignment, you’ll coordinate CQ activities for facilities, utilities, production equipment and computerized systems in a GMP environment. /ph3Your responsibilities /h3ulliDrive commissioning and qualification activities in line with project milestones, GMP requirements and site procedures. /liliDevelop and maintain CQ plans and schedules, particularly for construction and qualification phases. /liliPrepare, review and approve qualification plans, protocols, reports and acceptance criteria. /liliCoordinate colleagues, contractors and stakeholders across Engineering, QA, MST, suppliers and end-user teams. /liliSupport investigations, change controls, corrective actions and audit readiness. /li /ulh3Your profile /h3ulliDegree in Engineering, Life Sciences or a related scientific discipline. /liliAt least 3 years of relevant experience in a pharmaceutical GMP environment. /liliExperience in commissioning, qualification or validation; exposure to capital projects or oral solid dosage manufacturing is an advantage. /liliStrong planning, communication and problem-solving skills, with the ability to work independently and collaboratively. /li /ul #J-18808-Ljbffr