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 processes
* Developing and implementing automated visual inspection systems, managing electronic batch records, and supporting tech transfer activities for vaccine manufacturing processes
* Providing support for product validation activities, including the follow-up and support of various launch projects
* Documenting 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 degree
* Experience in an engineering, technical, or operations role within a GMP industrial environment, with proven expertise in projects and equipment qualification
* Strong analytical and problem-solving skills, a structured approach, and the ability to work both independently and as a team
* Excellent written and verbal communication and interpersonal skills are crucial for effective stakeholder interaction
* Proficiency in both Dutch and English is required
* Experience with process equipment, structured problem-solving methodologies (e.g., FMEA), and control systems (PLC, SCADA) is highly advantageous
* Some projects may require flexibility for shift work or weekend coverage