Description
The subsidiary tPM is seeking a Quality Management Specialist to develop, coordinate, and maintain its quality management system for medical devices, including AI-enabled Class IIa/IIb products. The role covers QMS documentation, regulatory compliance with MDR, IEC 62304, IEC 62366-1, ISO 14971, ISO 13485, and the AI Act, certification and audit support, quality data reporting, and process improvement. It is a part-time position generally requiring at least 30 hours per week, with 100% home-office work from Germany.
