Validation engineer aseptic manufacturing

Role and responsabilities: Commissioning and qualification of new and existing equipment Assuring appropriate risk management in the validation strategy Writing URS of pharma equipment Performing testing and validation activities (FAT and SAT) Ensuring that adequate documentation is available for operations and QA You will be working in cross-functional teams in a project or operational environment Your background: Experience in the pharmaceutical sector as validation or C&Q engineer Experience in commissioning and qualification of equipment or processes such as formulation, filling, cleaning, sterilization Candidate must speak fluent English. Italian is an asset. Dutch is not required. The location of the project is NORTHERN ITALY with a good airplane connection to Brussels Conditions: Full-time contract. (Freelance also possible) You will be part of a growing Belgian SME where initiative and personal development are encouraged. We will provide you with an enjoyable work environment with fun colleagues. Well work out a career plan with you, with attention and a budget for extra education/certification. You can count on an attractive salary, supplemented with extra-legal benefits, including a company car.