- Key responsibility for designing our new medical devices and supporting maintenance of released products.
- Key responsibility for analyzing concept/design solutions e.g. tolerance stack-up, structural analysis (both manual calculation and FEM).
- Create and maintain 2D and 3D documentation during development phases.
- Design test setups, and manufacturing tools.
- Conduct pre-engineering and verification testing related to design control requirements.
- Engage in problem-solving activities, root cause analysis, and NC & CAPA processes.
- Analyze the state of the art for similar products and assist in defining input requirements for projects, ensuring compliance with relevant standards.
- Prepare quality and technical documentation related to design, development, testing, and regulatory purposes.
Collaborate with cross-functional departments, clinical experts, regulatory officers, technical consultants, and suppliers.
- Minimum of 3 years of experience in R&D or a similar field
- Experience in designing for mass production
- Master’s degree or equivalent in engineering (preferably Mechanical or Mechatronic Engineering, Biomedical Engineering).
- Extensive experience with SolidWorks, and ideally also with Creo.
- Experience in designing small plastic parts for injection molding.
- Experience in designing small metal parts.
- Preferred experience and knowledge in the medical device industry.
- Strong organizational skills and a high sense of ownership.
- Enthusiasm for hands-on device testing and prototyping.
- Ability to work effectively in teams and prioritize tasks.
Proficiency in English (speaking, reading, and writing at B2 level or higher).
- The opportunity to develop cutting-edge technology that saves lives.
- Work in the R&D department within an international, interdisciplinary team.
- Interesting technical challenges.
- A great office atmosphere.
A range of benefits, including private medical care, sports card, flexible working hours, and English lessons.