**Are you our new Process Optimalization Engineer?** **Location: Weesp, Netherlands** **Department: Competence Center Influenza (CCI)** **Abbott Biologicals** , part of Abbott’s Established Pharmaceuticals Division (EPD), operates from Weesp and Olst. The Weesp site hosts three production facilities and several supporting (research) departments that provide global support. In our advanced facilities, qualified professionals produce active ingredients for medicines such as laxatives, hormones, and the flu vaccine. **Where will you work?** You will join the **CCI department** , a multidisciplinary team of laboratory technicians, scientists, process engineers, and project managers. The department supports influenza vaccine production processes and analytical release testing, while also driving process improvements and innovation. CCI collaborates closely with quality and regulatory departments, contributing to documentation and reporting. **What will you do?** As a **Process Optimization Engineer** , you will lead and contribute to technical projects within the CCI department, focusing initially on the commissioning and qualification of laboratory equipment. Over time, your responsibilities will expand to include the production facility. You will play a key role in multidisciplinary projects, requiring strong collaboration and communication across departments. Your tasks and responsibilities include: + Translating scientific and technological insights into clear improvement plans. + Becoming an expert in the technological aspects of influenza vaccine production. + Developing technical plans with realistic timelines. + Inventing, presenting and implementing process optimizations for upstream (USP) and downstream (DSP) process steps. + Acting as a change initiator for lab and production equipment. + Participating in commissioning and qualification activities (e.g., URS, FAT, SAT, C&Q). + Representing CCI in cross-functional project teams. + Growing into a **Production Project Lead (PPL)** role. **What do you bring?** + A completed bachelor’s or master’s degree in (Bio)Process Technology or a related field. + At least 5-10 years of relevant experience, preferably in the pharmaceutical industry. + Hands-on experience with equipment installation and qualification in a GMP environment. + Knowledge of USP/DSP processes such as centrifugation, filtration, and protein purification/characterization. + Strong analytical and systematic thinking skills. + Experience in project-based work and affinity with project leadership. + A proactive attitude and clear communication style. + Professional proficiency in **Dutch and English** . + Availability for a **full-time (40 hours)** position. **Why Abbott?** At Abbott, you’ll work in a dynamic and innovative environment where your contributions directly impact global health. We offer: + A collaborative and inclusive culture. + Opportunities for professional growth and leadership. + Competitive compensation and benefits. + A chance to be part of a mission-driven company improving lives worldwide. An Equal Opportunity Employer Abbot welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call 224-667-4913 or email corpjat@abbott.com