Senior Principal PM: Medical Software Strategy & Compliance

HeartFlow

San Francisco (CA)

On-site

USD 250,000 - 350,000

Full time

14 days+
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Benefits offered by this job

Medical / Dental / Vision (HeartFlow)
401k with employer match
Parental leave
Paid time off
EAP Program
Free snacks and drinks

Job summary

HeartFlow seeks a senior product leader to own the strategy for a portfolio of medical-grade products, shaping care delivery and evidence strategy across FDA-regulated software. You will be the deepest product-side expert on clinical workflow, validation, and real-world performance, guiding decisions across engineering, clinical, and regulatory leadership.

You will define multi-year portfolio plans, decide which problems to pursue, and frame options to build, partner, or acquire.

Qualifications

  • 15+ years of professional experience in product management for FDA-regulated software
  • BS, MS or PhD in Engineering, Science, or a related technical field; advanced degree or clinical training is a strong plus
  • Demonstrated ability to own a product area or portfolio at Principal/Director level and influence across functions

Responsibilities

  • Own multi-year portfolio strategy and decisions on what problems to solve
  • Define performance targets, evidence plans, and regulatory strategy for the portfolio
  • Align engineering, clinical, QA/RA, and marketing around a single product intent and roadmap
  • Maintain direct relationships with physicians and health-system customers to inform decisions
  • Lead FDA interactions, post-market surveillance, and design-controls across releases

Skills

FDA-regulated software
Customer orientation
Design and usability
Domain depth
Validation judgment
Strategic thinking
Regulatory fluency
Influence without authority
Product portfolio ownership
Leadership in PM

Education

BS/MS/PhD in Engineering/Science
Clinical training (strong plus)

Job description

HeartFlow seeks a senior product leader to own the strategy for a portfolio of medical-grade products, shaping care delivery and evidence strategy across FDA-regulated software. You will be the deepest product-side expert on clinical workflow, validation, and real-world performance, guiding decisions across engineering, clinical, and regulatory leadership.

You will define multi-year portfolio plans, decide which problems to pursue, and frame options to build, partner, or acquire.

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