Company Description
Founded in Munich, Germany in 1989, Brainlab develops, manufactures and markets software-driven medical technology, enabling access to improved, more efficient, less-invasive patient treatments. Our key to success is our creative, talented and hard-working team, which consists of around 2400 dedicated and inspiring individuals in 25 locations worldwide. To succeed in reaching our targets, we are seeking committed colleagues who can stand behind our core values curious, authentic and useful.
Job Description
We are looking for an additional (Senior) Project Engineer (with focus on Software) to join our R&D Imaging Endoscopy team!
Our focus is on developing innovative software and hardware solutions for neurosurgical endoscopy. The first focus for this position is to bring forward Endoscope Navigation 1.0. Looking ahead, we see exciting opportunities to integrate with robotics, video detection technologies and many other cutting-edge advancements. In addition, our long-term vision is to expand development into other clinical areas, as endoscopy plays a vital role across all segments in which Brainlab operates (spine, cranial, ENT, vascular).

As a member of our R&D Imaging Endoscopy team you will

• drive and support the product development process of software solutions
• take ownership over Risk Management activities for the software
• coordinate, define and execute verification and validation activities
• generate ideas, concepts and transfer them into medical devices

You will be part of a small but highly motivated, dynamic team and have the opportunity to push the boundaries of endoscopy to surgical navigation.

Qualifications

• University degree in biomedical, electrical or software engineering preferred, but other degrees may be considered (if coupled with medical relevant experience)
• Professional experience in the design and/or development of medical devices, especially in software risk management and validation activities
• Knowledge of medical device related standards and regulations such as FDA 21 CFR Part 820 and ISO 13485, IEC 60601, ISO 8600, IEC 62366
• Experience with technical documentation for medical devices
• Experience in working according to design control
• Well-organized and proactive working style
• Fluent written and spoken English

Please refer the Job description for details