Senior Director, AI Enabled Digital Products

Innovation starts from the heart. Our Advanced Innovation & Technology (AI&T) teams harness imagination, courage, and resourcefulness to think beyond what is currently possible and create solutions for patients many years into the future. If you are an early-stage innovator, the Edwards AI&T team is the place for you to take the next step in your career. We will give you the tools and resources you need to create groundbreaking innovations that shape the future of structural heart technology .        How you will make an impact:    Define intended use and claims for AI-enabled features, and own the related product requirements, roadmap, and lifecycle   Define the AI-enabled product portfolio strategy and sequence investments across therapy and workflow opportunities   Build and defend the business case and commercial model for AI-enabled therapy features   Validate product-market fit with clinicians, customers, therapy leaders, and commercial partners before scaling investment   Own adoption, product analytics, user feedback, and value realization after launch   Evaluate ecosystem, licensing, and partnership options when they accelerate differentiated product value   Partner with Clinical & Evidence AI on procedural-workflow features, owning the workflow as a shipped product while clinical teams own the correctness of the guidance itself   Define the predetermined change control plan that governs how the product can evolve after clearance       What you'll need (Required):    Bachelor's Degree in a related field plus 14 years of product management experience , with at least 5 years in a regulated software, medtech, or health-tech environment   A track record shipping AI-enabled products that achieved real adoption, spanning discovery, roadmap, lifecycle, and commercial model   Demonstrated ownership of product economics, market adoption, and cross-functional launch outcomes, not only roadmap delivery   Experience shipping at least one software product under formal design controls (ISO 13485, IEC 62304, or equivalent)   Direct experience managing an AI/ML product through its full lifecycle , including model versioning, retraining cadence, and performance drift after launch   Prior product leadership in medtech, health tech, or another FDA-regulated software environment   Experience partnering with regulatory and quality functions on submission-track products        What else we look for (Preferred):    Master's Degree or equivalent plus 12 years of product management experience , with at least 5 years in a regulated software, medtech, or health-tech environment   AI/ML product lifecycle management specifically: intended use definition, model versioning and retraining governance, and post-market performance tracking, distinct from general software product lifecycle work   Working familiarity with FDA Software as a Medical Device (SaMD) guidance and the predetermined change control plan (PCCP) framework   Verification and validation (V&V) planning and evidence generation for AI/ML-based products, including test protocol design for a model whose behavior is probabilistic rather than deterministic   Workflow integration design: embedding an AI feature into an existing clinical or procedural workflow without disrupting it, including human-factors and usability considerations for a physician-facing tool   Product requirements definition and roadmap ownership for a regulated, evidence-driven product, using tools such as Jira, Aha!, or Productboard   Product analytics and adoption measurement (Amplitude, Pendo, or equivalent)   Executive communication, portfolio judgment, and influence across Therapy, R&D, Clinical, Regulatory, Quality, Commercial, and Finance leadership   Excellent problem-solving, organizational, analytical , and critical - thinking skills , including sound discretion and judgment in decision - making   Expert understanding of business strategy, competitive landscape,