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Materialise

3D printing services, software tools, consulting

Medical Device Development Manager

Biomedical Engineering & Medical DevicesUpdated on Nov 15
Full-timeLeuven, BelgiumNo salary listedHybrid

About the Job

Requirements

  • A Master’s degree or PhD in Biomedical Engineering, Mechanical Engineering, Materials Engineering, or a related engineering discipline; an equivalent combination of education and relevant experience may be considered.
  • Five to ten years of experience in medical device development, preferably in orthopedic or CMF devices, implants, surgical instruments, or patient-specific solutions.
  • Demonstrated experience leading engineering teams or technical groups in a regulated environment.
  • Strong working knowledge of medical device design controls and product development processes.
  • A proven track record of bringing products through development to transfer or commercialization.
  • Experience working in cross-functional environments involving quality, regulatory, manufacturing, and clinical stakeholders.

Responsibilities

  • Lead, coach, and develop a team of device development engineers working on personalized and standard medical devices.
  • Set clear objectives and key results for each team member and follow up through periodic check-ins.
  • Build and maintain a high-performing engineering team with appropriate technical skills, regulatory awareness, and problem-solving capabilities.
  • Identify competency gaps and define training, mentoring, and development plans to ensure team readiness for current and future business needs.
  • Foster a culture of ownership, collaboration, innovation, quality, and continuous improvement.
  • Support resource planning, workload balancing, and prioritization across projects and product lines.
  • Recruit, onboard, and retain engineering talent aligned with company values and strategic needs.
  • Lead and contribute to development of standard and personalized 3D-printed guides and implants for various applications.
  • Translate clinical, business, and technical requirements into product development plans and engineering deliverables.
  • Drive product development activities across the design and development lifecycle, including user needs and design inputs, concept development, risk management, design outputs, verification and validation, design reviews, design transfer, and change management.
  • Collaborate with clinical, regulatory, quality, manufacturing, and commercial stakeholders to support product development and launch.
  • Ensure products are safe, effective, manufacturable, scalable, and aligned with customer and patient needs.
  • Ensure design control processes are implemented effectively and efficiently across development activities.
  • Drive compliance with applicable regulations and standards, including FDA 21 CFR 820, ISO 13485, ISO 14971, MDR, and other relevant medical device development guidance.
  • Improve development processes, templates, governance, and documentation practices to enhance compliance and development speed.
  • Promote pragmatic, right-sized process implementation that balances innovation, compliance, and operational efficiency.
  • Partner with Quality Assurance, Regulatory Affairs, Manufacturing Engineering, Clinical/Medical teams, Supply Chain, and Business Line management to execute development programs.
  • Act as a technical and organizational interface between R&D and other departments.
  • Align with other R&D teams in Paris and Rio Claro, Brazil, within the community of practice.
  • Communicate progress, risks, trade-offs, and resource needs to management and stakeholders.
  • Contribute to portfolio planning, technical roadmap discussions, and strategic decisions for orthopedic product lines.
  • Serve as an active technical contributor on selected orthopedic development projects.
  • Provide technical guidance in device design, materials selection, mechanical performance, patient-specific design considerations, and additive manufacturing processes.
  • Review and contribute to engineering documentation, design reviews, technical justifications, and problem-solving activities.
  • Support root cause investigations, design changes, and continuous product improvements across the product lifecycle.

Desired Qualifications

  • Experience with personalized devices, additive manufacturing or 3D printing, and/or orthopedic applications is highly preferred.

About the Company

Materialise

3D printing services, software tools, consulting

Materialise is a 3D printing provider offering prototyping, serial manufacturing, and personalized healthcare solutions. It combines high-precision printing with software that manages print workflows, file preparation, and production planning, plus consultancy to optimize designs. It serves automotive, aerospace, engineering, and healthcare industries and earns revenue from printing services, software licenses, and consulting. Its goal is to help customers turn ideas into scalable production, improve healthcare personalization, and advance sustainable, customer-focused manufacturing from prototype to volume production.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Leuven, Belgium
Founded
1990

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