Your responsibilities

• Design & Development: Design and development of custom and patient-matched medical devices for Medartis CMX service 

• Cross-Functional Collaboration: Collaborate closely with surgeons, R&D, manufacturing, and regulatory teams to deliver the custom made or patient matched devices on time to the operation room 

• Quality & Compliance: Ensure design and manufacturing processes comply with relevant medical device regulations (e.g., ISO 13485). Partner with Quality and Regulatory Affairs to maintain and improve quality standards

• Continuous Improvement: Participate in design reviews, risk assessments, and product validation activities. Identify opportunities to enhance product performance, reduce costs, and optimize manufacturing processes 

• Project Management: Coordinate cases and maintain clear case documentation 

Your qualifications

• Bachelor's or master's degree in biomedical engineering, mechanical engineering, or a related field. 

• Working experience in a clinical environment with 3D modelling or surgical planning 

• Excellent English skill in both written and spoke, German skills are an advantage 

• Proficient in 3d modelling. Familiarity with additive manufacturing, 3D printing, and other digital fabrication methods 

• Understanding of medical device regulations and industry standards (e.g., ISO 13485, FDA requirements)