Medical Process Engineer - 3D Printing & Validation

Materialise; Plymouth; On-site; GBP 63,000 - 97,000; Full time

Job summary

Materialise is seeking a Medical Process Engineer to join the Plymouth, MI team. You will collaborate with the global Production group on 3D printing, post-processing, cleaning and production planning, acting as a technical GoTo person for both development and operations.

You will drive validation programs, create documentation, and train operators, while working across operations, device development, biosafety, research, quality and regulatory teams to enable continuous improvement and growth.

Qualifications

• Master degree in engineering or equivalent through experience.
• Experience in a process (validation) engineering role within highly regulated industries (medical devices, pharmaceuticals or aerospace).
• Quality oriented with attention to detail and ability to think outside the box.
• Strong troubleshooting and problem solving skills.
• Proactive, self-organized, takes ownership of tasks.
• Value impeccable coordination.

Responsibilities

• Collaborate with global Production team on 3D printing, post-processing, cleaning and production planning; become a GoTo for development and operations.
• Identify, define, and implement process improvements following medical quality standards; use data to improve quality and efficiency.
• Maintain validation programs and complete new equipment, product and process validations; provide process documentation and training.
• Work with stakeholders from operations, device development, biosafety, research, quality and regulatory teams to shape growth.

Skills

Process engineering

Validation

Quality standards

Troubleshooting

Problem solving

Ownership

Cross-functional collaboration

Education

Master's degree in engineering

Experience in regulated industries

Job description

Materialise is seeking a Medical Process Engineer to join the Plymouth, MI team. You will collaborate with the global Production group on 3D printing, post-processing, cleaning and production planning, acting as a technical GoTo person for both development and operations.

You will drive validation programs, create documentation, and train operators, while working across operations, device development, biosafety, research, quality and regulatory teams to enable continuous improvement and growth.