Medical Informatics Specialist | Medizininformatiker (m/w/d) Siegen

Job Summary

The Medical Informatics Specialist will be responsible for the planning, conception, and implementation of demanding medical software for healthcare clients, ensuring strict compliance with regulatory requirements such as the Medical Device Regulation (MDR, IVDR) and FDA regulations. This role involves structured development of medical software within regulatory environments, contributing to software architecture concepts, specifications, and documentation. The ideal candidate holds a Bachelor's or Master's degree in Science, possesses initial project experience in developing robust, high-performance medical software, and has fundamental knowledge of key medical device standards (ISO/IEC 13485, 62304, 62366). Success in this position requires strong analytical skills, a solution-oriented approach, and excellent communication abilities, coupled with fluency in both German and English. This is a full-time, permanent position offering flexible hours and a hybrid work model in Siegen.