Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining what's possible and taking action.

　　How You Will Achieve It

　　Responsible for project engineering activities related to specific filling technology, equipment or process installationProvide technical input in the project team for own discipline, having technical and operational knowledge and expertise. Know how the installation or system functions and know the internal requirements (operational/technical/compliance).Define and documents the technical specs (Engineering Design Specification or technical spec, P&ID's, electrical diagrams) and review with the relevant SME.Follow the engineering standards and aligns with the lead engineer during design, construction and implementation.Follow up the construction, implementation and functioning of the equipment to guarantee the installation is according to spec.Guarantee good PM practices and tools (schedule, budget control, issues, decisions, reporting, stakeholder management, ...) for own equipment/installation/scope.Keep oversight of the contractor company that will build, install or test the equipment.Responsible for transfer to operations of own equipment, delivering all project documentation and close out of the project. Follow start up results to guarantee that the project deliverables were achieved.Assure correct documentation of construction and verification/validation on the engineering project folder.Responsible for defining and executing the engineering tests, verification and validation of own equipment. Define the validation approach, creates test protocols for engineering tests, creates verification and validation documents, executes tests, coordinates SME and system owner approvals. PE is responsible to solve and document deviations and actions (CAPA's, risk assessments, CGMP review, new document versions).

　　Qualifications

　　Must-Have

　　Master's Degree3+ years of experienceKnowledge of Good Manufacturing Practices and experience in Pharmaceutical environmentExperience of project orientated admin/cost control/managementBroad knowledge of theory and principles within a professional discipline or advanced knowledge of specific technical/operational practicesStrong technical, management and organizational skillsGood leadership and communication skills

　　Nice-to-Have

　　Relevant pharmaceutical experience

　　De Pfizer site in Puurs is één van de grootste productie- en verpakkingssites van Pfizer wereldwijd, gespecialiseerd in aseptische productie en verpakking. Jaarlijks worden in Puurs meer dan 400 miljoen doses injecteerbare vaccins en medicijnen geproduceerd. Deze zijn ter plaatse verpakt in ampullen, flacons, plastic flessen, spuiten en patronen voor pennen.

　　De medicijnen die in Puurs worden gemaakt, zijn bestemd voor patiënten in meer dan 170 landen wereldwijd. 30% van de productie uit Puurs is bestemd voor ontwikkelingslanden, in samenwerking met UNICEF, WHO, GAVI en ngo's.

　　Met het gebruik van twee windturbines, zonnepanelen en een warmtekrachtcentrale richten we ons op hernieuwbare energie.

　　Engineering