Systems Engineer

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Pharmaceuticals
The Company A leading pharmaceutical manufacturing organization focused on producing high quality medicines in a highly regulated environment. The company emphasizes quality, compliance, continuous improvement, and operational excellence across its production activities. About the Role This role is responsible for supporting and maintaining quality assurance activities within pharmaceutical manufacturing operations. The position focuses on ensuring GMP compliance, investigating deviations, driving CAPA initiatives, and supporting continuous improvement efforts. The successful candidate will work closely with production teams to enhance quality systems and maintain regulatory standards.
Company Our client is a global, innovation-driven organisation operating in a highly regulated manufacturing environment. The site focuses on reliable delivery of critical products and works to high quality and compliance standards. Teams collaborate closely across Manufacturing, Quality, Engineering and Technology to improve processes and keep operations running smoothly. Job Description We are looking for a Validated Systems Engineer to strengthen the Operations Technology team in Breda. This position sits at the intersection of digital technology and the production floor, helping to improve reliability, efficiency and compliance of packaging and labelling operations. The Validated Systems Engineer will support and improve a defined set of manufacturing systems (including SCADA and system integrations), working with site stakeholders and global teams to deliver practical solutions in a GMP-regulated environment. Responsibilities - Support the design, testing, qualification and change-control of manufacturing systems in line with GMP requi...