Principal/Director, Product Management

Required

• 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.
• 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.
• Strategic and quantitative rigor: Ability to frame ambiguous problems, size opportunities, reason under uncertainty, and defend a recommendation with data and explicit rationale.
• Influence without authority: A history of changing an organization’s direction through clarity and credibility rather than reporting lines.
• 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.
• Customer orientation: Deep curiosity about how clinicians actually work, and a habit of grounding decisions in observed practice rather than stated preference.
• Adaptability: Comfort where priorities, evidence, and constraints all change.
• 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.
• 15+ years of professional experience, with substantial time in product management for Software as a Medical Device, agile development, and regulated product development.
• Demonstrated experience owning a product area or portfolio at the scale expected of a Principal or Director-level individual contributor.