Materialise

What you will do

• Create test plans and define test strategies for manual and automated testing
• Perform manual and automated testing for Python-based applications
• Report test results according to test plans
• Create and update release testing documentation
• Help the product owner create requirements
• Participate in user needs discussions with customers and within a team
   

Your profile

• 2+ years of experience in manual/automated testing
• Solid knowledge of Python
• At least an upper-intermediate level of speaking and written English
• Strong interest in the medical field
• Open to learning new things
• Analytical thinking
• Excellent team player
• 3D mindset
• Out-of-the-box thinking
   

Nice to have

• Experience/knowledge of medical imaging (DICOM standard)
• Experience with Pydicom and NumPy libraries
• Experience with Docker and Linux
• Human anatomy knowledge

Mimics Enlight CMF is a workflow-based software to plan the surgical treatment of cranio-maxillofacial procedures. It contains separate workflows for the diagnosis and treatment planning of different indications within the cranio-maxillofacial field. Each workflow follows similar steps. First, the user creates 3D anatomical models by importing, visualizing, and segmenting the medical images of the patient. Next, the user plans the surgical treatment, making use of visualization and measurement tools. Last, the user can design personalized occlusal splints to transfer the plan to the operating room. The created models can be exported for 3D printing purposes.

The workflows in Mimics Enlight CMF are built on the Mimics Enlight platform. Mimics Enlight CMF and the Mimics Enlight platform are written for the Microsoft Windows family of operating systems and have a graphical user interface consistent with common Microsoft Windows applications.

 

Responsibilities:

— Design, build, and maintain efficient, reusable, and reliable C++ code.

— Identify bottlenecks and bugs and devise solutions to these problems.

— Help to maintain code quality, organization, and automatization.

— Take part in building and supporting cross-product platform.

— Code review and technical consultancies.

 

Requirements:

— At least 2 years of commercial experience in Software Development using C++.

— Mathematical background.

— Generic programming and templates, STL.

— At least an intermediate level of English.

— Agile/Scrum mindset.

 

Will be a plus:

— Python is a plus.

— Experience with Qt Widgets is a plus.

— Experience in UI programming.
— Boost skills.

Join our Medical Software department as a Software Development Engineer С++.

Responsibilities:

• Design, develop, and maintain efficient, reusable, and reliable C++ code for developing an Industry-standard 3D medical image segmentation software
• Identify and resolve performance bottlenecks and bugs, ensuring robust and high-quality software deliveries.
• Uphold and improve code quality, organization, and automation processes across the development team.
• Collaborate in the development and support of cross-product platforms to foster integration and seamless functionality.
• Develop user interfaces using QT, focusing on creating intuitive and user-friendly experiences.
• Conduct code reviews and provide technical consultancy to team members, promoting best practices and continuous improvement.
• Create detailed design specifications that guide the development and implementation of new features and enhancements.
• Integrate desktop products with cloud services, enhancing connectivity and expanding functionality.
   

Requirements:

• Proven experience in software engineering with a strong focus on C++ development.
• Expertise in identifying and resolving software bottlenecks and bugs.
• Demonstrated ability to maintain high code quality and organization.
• Experience in cross-product platform development and support.
• Strong skills in code review and providing technical guidance.
• Ability to create clear and comprehensive design specifications.
  English language proficiency (at least B2 level, ability to communicate with colleagues in multinational environment).

Will be a plus
Degree in Engineering, Math, Physics, or similar.
Knowledge of QT for user interface development.
Experience with cloud integration for desktop products.

Mimics software allows you to process and edit your 2D image data (CT, MRI, etc.) to construct 3D models with the utmost accuracy, flexibility, and user-friendliness. The powerful segmentation tools allow you to segment your medical CT/MRI images, take measurements, and engineer directly on your 3D model. From there you can export your 3D data to a wide range of output formats and engineering applications; such as FEA, design, surgical simulation, additive manufacturing, and more. 

In this role, you will be instrumental in developing Python-based applications that automate our medical services, contributing to our innovative SuperNova Python framework, and supporting various projects through detailed technical analysis and documentation. In this position, you will work closely with researchers, process and service engineers.

Responsibilities:

- Develop Python-based applications for Medical services automation.

- Contribute to internal Python framework.

- Create and update development documentation (SDS).

- Help the product owner and product manager define technical details for implementation.

- Contribute to project requirements analysis.

Requirements:
- 2+ years of experience in software development.
- Strong knowledge of Python.

- Analytical thinking.

- Excellent team player.

- Experience with medical imaging (DICOM standard, etc.)

- At least Upper- Intermediate level of speaking and written English.

Preferred skills:

- Experience with Linux and Docker.

- A good understanding of and experience with OOP.
- Strong interest in the medical field.
- Spatial thinking.
- Experience with cloud infrastructure for AI.

Are you passionate about healthcare and technology? Join our company as a Quality Manager.


Key Responsibilities:

• You are responsible for the global medical quality system, allowing global compliance to corporate and local quality procedures and to regulatory requirements. The scope is the global medical quality management system compliance, and the interactions with entities not fully integrated (i.e. Materialise Southampton).
• Management representative, when appointed, responsible for ensuring that processes needed for the quality management system are documented, reporting to top management on the effectiveness of the quality management system and any need for improvement, ensuring the promotion of awareness of applicable regulatory requirements and quality management system requirements throughout the organization, Materialise Japan, Materialise Colombia, Materialise Southampton, Materialise USA.
• You ensure that Corporate Medical and business/service unit Management Reviews are held in accordance with applicable standards and procedures, and that relevant data is gathered.
• You monitor the status of medical regulatory projects to ensure regulatory compliance for distribution activities across the world. To this end, you are a functional manager to the regulatory affairs project manager and senior regulatory affairs officer. You monitor, among others, company registrations, product registrations, vigilance activities, regulatory notification/reporting.
• Monitor, via team members more directly involved, the status of medical labeling (claims) projects to ensure regulatory compliance with technical files across the world with regulatory officers, including labels, instructions for use, marketing pieces, social media
• Ensure implementation of quality management system within corporate global and local management teams, as an example, Purchasing system/Supplier Evaluations, Document Control, Electronic Documents/Records. Liaise with the Medical Business Unit’s Director of Operations team to ensure streamlined application of the QMS principles throughout Quality Management, Production and Process Engineering.
• Champion FDA compliance at all Materialise locations, ensuring successful inspections, which you will attend and steer.
• Follow-up of non-medical software development activities but only to ensure uniformity with medical software development. Liaise with SAM quality.
• Mentor Quality Engineer MatUSA, Point of Contact for MatUSA with FDA; coordinate with the MatUSA Managing Director where needed in this respect.
• Business trips 4 times per year to UK and Spain
  
   

Required Skills & Qualifications:

• Degree educated in Business, Computing, Science, Medical, or Mathematical Based Discipline. These qualifications are documented within individual personnel records.
  
   

Experience

• Applicant should be an experienced quality manager with 5+ years of experience in managing a quality system, with particular experience of Medical Device Regulations (US, EU, Canada, Japan, Australia, Brazil, etc.,). Pre-joining experience is documented within individual personnel records.
• Ability to analyse regulatory documentation and to derive the necessary changes needed to conform (demonstrated in interview or from in house performance).
• Demonstrated understanding of the importance of quality — including good practices, understanding of the importance of process and documentation (demonstrated in house or through interview and relevant experience).
• Experienced in delivery of quality systems in a software environment (demonstrated through previous held positions and projects).
• Knowledge of key medical software regulation practices and procedures and the auditing processes associated with them (demonstrated in interview or from in house performance).
• Possession of good communication skills (demonstrated through interview or in house performance).
• Great attention to detail and quality first mentality (demonstrated in interview or from in house performance).