Biosafety Engineer

MAT CZE Materialise SRO

Vlaams-Brabant

On-site

EUR 60,000 - 90,000

Full time

2 days ago
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Job summary

Materialise Medical is seeking a Biomedical Engineer to join the Medical Business Unit, focusing on biocompatibility, cleaning, packaging and sterilization of medical devices.

You will collaborate with regulatory, development and manufacturing teams to ensure safety and compliance, support ISO 10993-1 activities, develop validation protocols, and drive improvements across processes.

Qualifications

  • Master's degree in engineering, biochemistry, biology or medical fields.
  • Knowledge of regulatory requirements for biocompatibility evaluation and sterilization validation.
  • Ability to manage multiple projects and set priorities.
  • Effective teamwork and independent decision-making to meet goals.
  • Clear verbal and written English communication.
  • Analytical mindset with meticulous attention to detail.

Responsibilities

  • Ensure biocompatibility of medical devices and develop/validate cleaning, packaging, and sterilization processes.
  • Support biological safety evaluations per ISO 10993-1 and validation of cleaning/sterilization processes.
  • Develop new or optimized packaging for sterile and non-sterile devices and test performance.
  • Set up and monitor programs to verify regulatory and quality requirements.

Skills

Biocompatibility
Sterilization validation
English communication
Regulatory knowledge
Project management

Education

Master's degree

Job description

At Materialise Medical, we believe that better healthcare starts with solutions designed around the individual patient. If you're passionate about bringing personalized care to every patient, you'll love being a part of this team. Through the technology we develop, researchers, engineers, and clinicians are revolutionizing personalized treatment - helping improve and save lives daily.

Responsibilities
  • Within the Medical Business Unit, you are part of the team of specialists that ensure the biocompatibility of our medical devices and that develop and validate their cleaning, packaging, and sterilization processes.
  • You participate in medical device development by supporting biological safety evaluations in accordance with ISO 10993-1 and by executing cleaning and sterilization process validations.
  • In addition, you develop new or optimized packaging for sterile and non-sterile medical devices and test their performance.
  • You set up and take part in monitoring programs to ensure continued fulfillment of requirements.
  • You contribute to regulatory submissions of new devices.
  • You build a thorough understanding of the manufacturing process, especially the steps related to cleaning, packaging, and sterilization, to effectively plan new development and validation activities.
  • You create and finalize validation protocols and reports, ensuring they are clear, concise, and compliant with work instructions and standards.
  • You assess the impact of the process or product changes and propose adequate actions.
  • You plan and follow up on test sample production with the manufacturing team and with suppliers.
  • You coordinate the tests that are being performed at external test labs.
  • You interact closely with internal stakeholders (including the Quality, Regulatory, Development, Process Engineering, and Manufacturing teams) and external partners (including test labs and suppliers) to ensure good communication and swift collaboration.
  • You act as an ambassador and safeguard of biological safety within Materialise Medical.
Requirements
  • Master degree (engineering, biochemistry, biology, or medical)
  • Knowledge and understanding of regulatory requirements, standards, and guidance documents in the field of biocompatibility evaluation, cleaning validation, packaging development, or sterilization validation of medical devices.
  • Able to work on multiple projects simultaneously, set priorities, and establish short- and long-term planning horizons.
  • Effective as a team member to accomplish project deadlines and objectives, yet able to work and make decisions independently to reach goals.
  • Clear and effective verbal communication and technical writing skills in English.
  • Good analytical skills, meticulous approach with a high level of attention to detail.
  • Passionate about patient safety and customer satisfaction
What's waiting for you
Work that matters

The technology we build at Materialise pushes the boundaries. You'll find pride in building something that matters, whether you designed it, printed it, or shipped it. No matter your role, we unlock new possibilities to build a better and healthier world every day.At Materialise, we expect you to think about the customer, not just the task. You push for better solutions and care about the difference your work makes.

A people-centered space

When you join Materialise, you join a group of colleagues invested in you, not just your work. From your own team to a department across the world, you'll find a sense of belonging with people who help without being asked, challenge you, and have your back.At the same time, we expect you to invest in the people around you - not just your own work - to make the group stronger than the sum of its parts.

An environment of trust

As a company of innovators, we know how crucial autonomy is in your work. When we hire you, we trust in your expertise, giving you space to organize your tasks, work flexibly, and make your own calls.At Materialise, we expect you to deliver on that trust and keep your commitments.

A career ready to build

When you see opportunities for your career to grow at Materialise, we encourage you to go for them. People shape a fulfilling career at their own pace here.At Materialise, we expect you to take initiative in your own development. Don't wait for someone else to plan your career. Step into the space and make it count.

Make a difference together with the Medical team.

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