The posting
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.



