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As a Process Engineer you will be responsible for technical, operational, compliance, and qualification support for GMP and non-GMP systems within manufacturing and R&D environments in Belgium, including the site. This encompasses project management and execution of discrete work scopes for overall project delivery, with a strong focus on process design, equipment validation, and continuous improvement.Identifying and resolving production bottlenecks, conducting root cause investigations for quality deviations, implementing changes to existing equipment, and supporting the introduction and validation of new products and processesDeveloping and implementing automated visual inspection systems, managing electronic batch records, and supporting tech transfer activities for vaccine manufacturing processesProviding support for product validation activities, including the follow-up and support of various launch projectsDocumenting qualification work in aseptic manufacturing and engineering.Qualifications:Master's degree in a relevant engineering field such as industrial, civil, bio-engineering, chemical, or mechanical engineering, or hold an industrial pharmacist degreeExperience in an engineering, technical, or operations role within a GMP industrial environment, with proven expertise in projects and equipment qualificationStrong analytical and problem-solving skills, a structured approach, and the ability to work both independently and as a teamExcellent written and verbal communication and interpersonal skills are crucial for effective stakeholder interactionProficiency in both Dutch and English is requiredExperience with process equipment, structured problem-solving methodologies (e.g., FMEA), and control systems (PLC, SCADA) is highly advantageousSome projects may require flexibility for shift work or weekend coverage