Responsibilities
- Define and maintain the product vision, roadmap, and prioritized backlog for the Patient Viewer.
- Convert clinical and business requirements into detailed user stories and acceptance criteria.
- Collaborate closely with XR engineering teams on Unity, Android XR, hand tracking, spatial UI, and DICOM/NIFTI rendering.
- Ensure product decisions align with MDR, IEC 62304, and ISO 13485 standards, coordinating with Quality and Regulatory teams on requirements, risk management, and traceability.
- Engage with clinicians, partners, and internal teams to gather and organize feedback.
- Manage release cycles, app store preparation, and define measurable product objectives.
- Assist the global sales team in their efforts.
Nice to Have
- German language skills are advantageous.
- Experience with regulated medical software under EU MDR, IEC 62304, and ISO 13485.
- Familiarity with medical imaging formats such as DICOM, NIFTI, STL, or GLB.
- Background in a clinical setting or experience working with healthcare professionals.
Benefits
- Opportunity to work on a product with tangible clinical impact at the intersection of XR and medicine.
- Short decision-making paths and high ownership within a focused team.
- Collaboration with international partners and pioneering work in a rapidly growing field.
- Flexible hybrid working arrangement with a base in Hamburg.
Work Arrangement
Hybrid — Hamburg
Other
- Fluent in English; German is a plus.
- Flexible, hybrid working with a base in Hamburg.