Validation Engineer We are looking for a Validation Engineer. You will be working in our newest plant where we make products for the healthcare market. A new plant for the production of cell culture media is being built at our location in Tilburg. Cell culture media are raw materials for the biopharmaceutical industry, where they are used for the production of medicines or vaccines. For this new production facility we have a vacancy for a Validation Engineer in the department Quality Systems / Regulatory Affairs (QS/RA). The position Within Life Science Manufacturing (LSM), the QS/RA department is responsible for all activities relating to quality. This includes the approval of raw materials, the release of finished products and all tests on these materials, but also supplier evaluations, deviations during production and change control. Document control also falls under this department. As Validation Engineer, you are responsible for carrying out and setting up various validations; both on equipment and for various processes and production. In addition, you support the writing of procedures and protocols for this. You are also involved in the evaluation of existing processes and in change control, deviations and CAPAs around validations. Together with the validation specialist, you are responsible for ensuring that all equipment, utilities and processes are and remain in a validated state.