Embedded Software Developer for Medical Devices | Entwickler Embedded Software für Medizingeräte (m/w/d)

LRE Medical GmbH

München, Bayern, Deutschland
Published Feb 24, 2026
Full-time
No information

Job Summary

This role involves the development of embedded software for sophisticated medical and diagnostic systems at LRE Medical's Munich location. As part of an interdisciplinary project team, you will be responsible for the entire software lifecycle, including system analysis, architecture design, and implementation of firmware. You will work closely with electronics development to integrate hardware and software, ensuring high-quality standards for medical diagnostics. Key tasks include documenting requirements, integrating external software components, and designing development-related tests. This position is particularly attractive for those who enjoy working on complex systems involving optics, mechanics, and electronics. The company offers a dynamic environment with flexible working hours and the opportunity to see a product move from initial development through to production handover. You will act as a technical bridge, communicating with internal departments, customers, and suppliers to deliver innovative analytical systems.

Required Skills

Education

Successfully completed degree in Electrical Engineering, Electronics, (Medical-Technical) Computer Science, or a comparable field of study.

Experience

  • At least 3 years of relevant experience in embedded software development, preferably in device development
  • Several years of experience in programming real-time systems using C or C++
  • Professional experience with operating systems such as FreeRTOS or Embedded Linux
  • Proven experience in implementing communication protocols and working with hardware interfaces
  • Practical experience in hardware-related software development using oscilloscopes and logic analyzers

Languages

German (Fluent)English (Fluent)

Additional

  • Must be able to work on-site in Munich, Germany. Requires the ability to document technical requirements and solutions according to internal guidelines and medical industry processes.