Process Engineer Aseptic Manufacturing

Role and Responsibilities: You write the specifications for new formulation equipment. You are part of a project team or you lead the project yourself. You organize technical/process technical meetings with your suppliers. You guide the design, basic and detailed engineering activities of the installation/equipment constructors. You organize the testing of the equipment (FAT en SAT). You coordinate startup in operations and handover to production. Your Background: Knowledge and experience in pharma formulation processes. Knowledge of CIP (clean in place) and SIP (sterilize in place) processes and equipment. Master level engineer or bioengineer. Experience with vaccine formulation is an asset. Experience in a pharmaceutical (or life science) environment is an asset (GMP). Requirements: 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. We'll 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. #J-18808-Ljbffr