Principal or Director of Product Management

Join HeartFlow, a pioneering company in the field of cardiovascular disease diagnosis and treatment. As a Principal or Director of Product Management, you will shape the future of care delivery by owning the strategy for a portfolio of medical-grade products. You will be the company's deepest product-side expert on clinical workflow, validation, and real-world performance, and your success will be measured by the quality of decisions the organization makes because of you.

• Définir et posséder la stratégie de portefeuille pour une gamme de produits médicaux, en identifiant les problèmes à résoudre et en séquençant les priorités.
• Agir en tant qu'expert en matière de flux de travail clinique, de validation et de performance réelle, en prenant des décisions éclairées qui influencent l'organisation.
• Aligner les équipes interfonctionnelles autour d'une intention produit unique, en construisant un modèle mental partagé qui permet à ces équipes d'agir sans attendre.

• Track record: Extensive product management experience with FDA-regulated software, including at least one product taken from concept through clearance or approval and into routine use
• Adaptability: Comfort where priorities, evidence, and constraints all change
• Customer orientation: Deep curiosity about how clinicians actually work, and a habit of grounding decisions in observed practice rather than stated preference
• Design and usability standard: Strong instincts for visual design, workflow, and usability, and a high bar you hold others to — especially where product output meets interpretation and decision-making
• Domain depth: Real depth in a relevant area — cardiovascular disease, diagnostic imaging and interpretation, multimodal risk assessment, disease pathogenesis, or decision support — enough to hold your own with physicians and in a technical review
• Validation judgment: Fluency in how medical products are validated: study and dataset design, generalization across patient populations and sites, sensitivity and specificity trade-offs, and the gap between a benchmark result and real-world performance
• Strategic and quantitative rigor: Ability to frame ambiguous problems, size opportunities, reason under uncertainty, and defend a recommendation with data and explicit rationale
• Regulatory fluency: Working command of design controls, risk management, V&V, human factors, and post-market obligations — enough to shape strategy with QA/RA as a peer
• Influence without authority: A history of changing an organization’s direction through clarity and credibility rather than reporting lines
• Demonstrated experience owning a product area or portfolio at the scale expected of a Principal or Director-level individual contributor
• 15+ years of professional experience, with substantial time in product management for Software as a Medical Device, agile development, and regulated product development
• BS, MS, or PhD in Engineering, Science, or a similar technical discipline. An advanced degree or clinical training in a relevant field is a strong plus