• Define and drive the roadmap for one or more Qu product capabilities. • Collaborate closely with clinicians and regulatory experts to ensure all features meet safety, privacy (GDPR/HIPAA), and MDR/FDA medical device standards. Previous work with ISO13485 and ISO14971 is a plus. • Use data and experimentation to improve key product metrics — adoption, engagement, and quality scores (precision/recall, OSCE pass rates, etc.). • Translate complex clinical and technical concepts into clear product requirements and user stories. • Partner with engineering and AI teams to scope features that balance innovation with safety and compliance. • Champion user needs — both clinicians and enterprise customers — to prioritize features that deliver measurable value.