Process Engineer: Additive Manufacturing for Medical

MAT BEL Materialise NV; Heverlee; On-site; EUR 60,000 - 80,000; Full time

Job summary

Materialise Medical in Leuven seeks a Process Engineer to join the HQ Process Engineering team. You will drive cross-functional agile projects on CMF product development, manufacturing process development, and implementation, applying your engineering mindset to additive manufacturing, post-processing, cleaning and quality inspection.

You lead validation programs, assess manufacturability, support design transfer, and set up process characterization studies to understand parameter effects.

Qualifications

• Master's degree in engineering or related field.
• At least 2 years of experience in process (validation) engineering in regulated industries (medical devices, pharmaceuticals or aerospace).
• Experience with Design Transfer activities and/or Additive Manufacturing is a strong plus.
• Strong eye for detail, proactive and able to think out of the box.

Responsibilities

• Lead larger process development, implementation and validation projects across teams.
• Assess manufacturability and process validation needs in early development.
• Define product specifications input for process validation and implementation after design transfer.
• Own validation programs for manufacturing processes and equipment (IQOQPQ).
• Drive standardization and automation of process steps to enable scalability and operational excellence.

Skills

Process engineering

Validation

Project management

Troubleshooting

Problem solving

Quality mindset

Self-organized

Additive Manufacturing

Education

Master's degree in engineering

Tools

IQ/OQPQ

Additive Manufacturing

Job description

Materialise Medical in Leuven seeks a Process Engineer to join the HQ Process Engineering team. You will drive cross-functional agile projects on CMF product development, manufacturing process development, and implementation, applying your engineering mindset to additive manufacturing, post-processing, cleaning and quality inspection.

You lead validation programs, assess manufacturability, support design transfer, and set up process characterization studies to understand parameter effects.