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Development engineer

Louvain
Materialise
De 80 000 € à 120 000 € par an
Publiée le 4 novembre
Description de l'offre

What you will do

Research and innovation activities:

* Collaborate closely with surgeons to understand clinical challenges and gather input
* Identify and analyze market and user needs specific to soft tissue surgery innovations
* Translate user and market needs into actionable technical requirements
* Stay updated with the latest scientific and technological advancements in 3D printing and soft tissue surgery applications
* Assess the technical feasibility of innovative 3D-printed solutions for soft tissue surgery

Development activities:

* Design and develop new 3D-printed medical devices tailored for soft tissue surgery
* Prepare and maintain technical documentation, including design history files (DHF) and technical files
* Define and execute verification and validation activities for prototypes and final designs
* Plan and support the transfer of designs to production teams
* Manage and maintain technical communication with external partners and subcontractors

Executional and process engineering activities:

* Build a hands-on understanding of 3D printing processes, post-processing, and quality assurance methods
* Contribute to small-scale tasks, such as assembly, testing, and quality inspection of prototypes
* Identify and implement process improvements to optimize efficiency and scalability
* Support the development of workflows and documentation (e.g., work instructions) for new product introductions
* Ensure the seamless transition of R&D innovations into market-ready solutions

Your profile

Must-haves:

* A master's degree in biomedical engineering, mechanical engineering, materials science, or a related technical field.
* Strong communication skills and the flexibility to change gears whenever needed, with a start-up mentality.
* Proficiency in English (spoken and written), particularly for creating technical documentation and collaborating with diverse stakeholders

Nice-to-haves:

* Experience designing and developing medical devices or other regulated products
* Familiarity with medical device regulations and quality management systems (e.g., ISO 13485)
* Able to think strategically about product development while engaging in small, detail-oriented tasks
* Comfortable working in a small, dynamic team with tight deadlines
* Strong problem-solving skills, creativity, and a hands-on approach to challenges
* Excellent communication skills to interact effectively with team members, surgeons, and external partners
* Demonstrated ability to adapt, plan, and execute tasks with minimal supervision

Location and type of contract

* Leuven (HQ), Belgium
* Full-time
* Hybrid
* Mid-senior level
* CV in English

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