Computer-Stellen für Engineering

. • Coordination and cooperation with third-party suppliers and contractors • Supporting project management in planning software-related tasks • Collection and determination of technical requirements • Support of trouble shooting in production related to software issues • Sustaining of existing products / systems to ensure stable and reliable operations a spart of the product lifecycle management process b) Documentation • Adherence of projects goals, national and international standards and regulations (CE, FDA, MDR…) • Create documentation according to regulatory requirements in the strongly regulated field for medical devices, like requirements, specifications, risk analysis and verification documents Ihr Profil • Graduate in engineering or computer science or Technical education (e.g. staatl. gepr. Techniker) with adequate experience • Proven working experience of 5 years+ of software engineering in the embedded field • Experience in coordinating software-related tasks and assisting with project planning is desirable • Experience in a regulated environment, preferably in the field of regulated medical devices or a different domain • profound knowledge in Ansi C, C++ • experience with interfaces like RS232, RS485, CAN • experience with RTOS, Yocto and QT • experience with git, make, gcc are a plus • Quick learner • proactive attitude and strong teamplayer • Systematic work ability and high-quality awareness Warum wir?