Responsibilities: Assist in the design and development of medical devices (such as implants and catheters) using CAD software. Prepare all necessary documentation for product approval, ensuring compliance with current medical technology regulations. Develop and continuously improve production processes. Perform minor adjustments to tools as needed. Plan, execute, and document various tests. Coordinate with development, production, and quality assurance teams to make drawing adjustments. Support the QA/RA department in validating production processes. Qualifications: Completed technical studies or training in medical technology, plastics technology, mechanical engineering, or a related field. Professional experience in product development within a medium-sized medical technology company, including CE approval. Proficiency in CAD software, preferably SolidWorks. Strong written and verbal English communication skills. Demonstrated entrepreneurial mindset, resilience, and attention to detail in documentation.