Your Tasks

• Development of new implantable components and their manufacturing processes
• Creation of documents (specifications, test reports, development documents) and management of them within the quality system
• Collaboration with and coordination of external suppliers
• Planning and execution of verification & validation tests
• Supporting the production transition

Your Profile

• MSc degree or higher (University, FH) in the field of mechanical engineering, medical technology or comparable qualification
• First professional experience in medical technology is an advantage
• Experience with design (SolidWorks) and in quality management is an advantage
• Independent, self-organized, precise and structured way of working as well as motivation to work independently and in a team
• Good oral and written communication skills in German and English