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.