deepeye Medical GmbH

Support distribution partners in implementing AI software for ophthalmologists and train customers to maximize the value of the AI assistant. Present solutions at conferences and provide product feedback to the management team to improve the tool.

Lead the preparation and quality control of Clinical Evaluation Plans (CEP) and Reports (CER) in accordance with EU MDR regulations. Translate clinical and technical data into scientific manuscripts and white papers while collaborating across R&D and regulatory teams.

Develop full-stack medical software for vision loss prevention in compliance with quality management systems. Responsibilities include system integration, rigorous testing, and managing deployment within Windows or Cloud environments.