Medical Process Engineer - 3D Printing & Validation Specialist

Mondeadditif

Plymouth

On-site

GBP 67,000 - 89,000

Full time

7 days ago
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Job summary

Materialise is seeking a Medical Process Engineer to join the US team in Plymouth, Michigan. You will collaborate with global production on 3D printing, post-processing, cleaning and production planning, driving process improvements and validation activities.

You will validate equipment, products and processes, develop documentation and training materials, and support quality and regulatory efforts across multiple teams to enable safe, efficient patient-specific solutions.

Qualifications

  • Master's degree in engineering or equivalent
  • A few years of experience in a process (validation) engineering role in highly regulated industries such as medical devices, pharmaceuticals or aerospace
  • Strong problem-solving and troubleshooting skills
  • Quality oriented with attention to detail and proactive approach
  • Owns tasks with initiative and collaborative mindset

Responsibilities

  • Work with global Production team on 3D printing, post-processing, cleaning and production planning topics
  • Define, implement and document process improvements in line with medical quality standards
  • Validate equipment, products and processes and update work instructions and training materials
  • Provide operational support to ensure quality and efficiency of processes
  • Collaborate with stakeholders from quality, regulatory, device development and biosafety teams

Skills

Process engineering
Validation
Troubleshooting
Quality mindset

Education

Master's degree in engineering

Job description

Materialise is seeking a Medical Process Engineer to join the US team in Plymouth, Michigan. You will collaborate with global production on 3D printing, post-processing, cleaning and production planning, driving process improvements and validation activities.

You will validate equipment, products and processes, develop documentation and training materials, and support quality and regulatory efforts across multiple teams to enable safe, efficient patient-specific solutions.

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