Process Engineer - Medical Devices & Validation Expert

MAT CZE Materialise SRO; Plymouth; On-site; GBP 55,000 - 75,000; Full time

Job summary

Materialise is seeking a process engineer to join our Medical team in the UK. You will work with the global Production team on validation, process improvements and production planning for 3D printing, post-processing, and cleaning.

With a Master’s degree in engineering and experience in regulated industries, you will define and implement quality-driven validations, develop documentation, train operators, and collaborate across operations, device development, biosafety, quality and regulatory

Qualifications

• Master degree in engineering or equivalent.
• Experience in process (validation) engineering in highly regulated industries such as medical devices, pharmaceuticals or aerospace.
• Detail-oriented with ability to think outside the box when needed.
• Strong troubleshooting and problem-solving skills.
• Proactive, self-organized, take initiative and own your tasks.
• Value and uphold impeccable coordination with stakeholders.

Responsibilities

• Work with the global Production team on topics related to 3D printing, post-processing, cleaning & production planning.
• Identify, define, and implement process improvement following medical quality standards on documentation and validation of your work.
• Maintain existing validation programs and complete new equipment, product and process validations; provide process documentation and operator training.
• Collaborate with stakeholders from operational, device development, biosafety, research, quality and regulatory teams to shape growth trajectory at Materialise.

Skills

Quality mindset

Troubleshooting

Proactive work ethic

Ownership

Coordination

Education

Master's degree in engineering

Job description

Materialise is seeking a process engineer to join our Medical team in the UK. You will work with the global Production team on validation, process improvements and production planning for 3D printing, post-processing, and cleaning.

With a Master’s degree in engineering and experience in regulated industries, you will define and implement quality-driven validations, develop documentation, train operators, and collaborate across operations, device development, biosafety, quality and regulatory