- Own the product end-to-end: from feature scoping through implementation, launch, and international roll-out
- Translate medical and business requirements into clear technical specifications and a prioritized backlog, based on input from users, markets, and internal stakeholders
- Support the MDR process by bringing technical and product input into Regulatory's decisions on intended use, risk, and output presentation
- Own the software requirements specification (SRS) and work closely with our AI team to specify and integrate the MDR-certified AI system into the product
- Work with the product team to bring the device live across multiple markets on our existing platform, adapting to local requirements where needed