About this role
Do you want to help ensure the quality of systems and processes at a leading pharmaceutical company? Select Projects is seeking a Qualification Engineer for an assignment with our client in Geel. You will support the engineering team in qualifying equipment throughout its entire lifecycle. Your responsibilities: Reviewing and approving qualification and validation documents (SOPs, URS, risk assessments, test plans, scripts, change controls, CAPAs, etc.) Supporting engineering teams with the introduction of new or updated systems and processes Providing advice on cGMP aspects and compliance during qualification and validation activities Following up on deviations and communicating status updates to QA teams You hold a professional bachelor’s or master’s degree in a scientific or technical field (e.g., industrial sciences, bioscience engineering, etc.). You have proven work experience with qualification or validation activities in the pharmaceutical sector. You are knowledgeable about GMP, GDP, and safety documentation. Experience with change control management (preferably using TrackWise) is an asset. You have strong verbal and written communication skills.