3 дня назад
Principal/Director, Product Management (AI MedTech)
240 000 - 295 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Principal/Director, Product Management (AI MedTech): Owns the multi-year strategy and performance commitments for a portfolio of FDA-regulated AI-driven cardiac products with an accent on clinical workflow, validation, regulatory evidence, and real-world outcomes. Focus on defining product requirements, shaping FDA and evidence strategy, resolving cross-functional trade-offs, and building products physicians can trust across the coronary care pathway.
Location: San Francisco, California, United States
Salary: $240,000–$295,000 yearly base compensation, plus cash bonus and equity.
Company
is a publicly traded medical technology company developing AI-driven, non-invasive products for the diagnosis and management of coronary artery disease.
What you will do
- Own the multi-year strategy for a portfolio of medical-grade cardiac products, including roadmap sequencing and build, partner, or acquire decisions.
- Define performance targets, acceptable failure modes, intended-use boundaries, patient populations, and product claims with Clinical and Regulatory teams.
- Map and optimize the end-to-end care pathway, covering referral, image acquisition, interpretation, reporting, follow-up, and reimbursement.
- Author user needs and system requirements for complex problems and resolve contested requirements across functions.
- Shape FDA interactions, pre-submission planning, verification and validation, evidence design, and post-market surveillance.
- Align engineering, data science, UX, human factors, clinical, QA/RA, marketing, and support teams while engaging physicians, advisors, and health-system customers.
Requirements
- Extensive product management experience with FDA-regulated software, including taking at least one product from concept through clearance or approval and routine use.
- 15+ years of professional experience, including substantial experience with Software as a Medical Device, agile development, and regulated product development.
- Deep expertise in cardiovascular disease, diagnostic imaging and interpretation, multimodal risk assessment, disease pathogenesis, or clinical decision support.
- Fluency in clinical validation, including study and dataset design, population and site generalization, sensitivity and specificity trade-offs, and real-world performance.
- Working knowledge of design controls, risk management, V&V, human factors, and post-market obligations.
- BS, MS, or PhD in Engineering, Science, or a similar technical discipline, plus experience owning a Principal- or Director-level product area or portfolio.
Nice to have
- Advanced degree or clinical training in a relevant field.
- Strong visual design, workflow, and usability judgment.
Culture & Benefits
- Senior individual-contributor track with Principal and Director levels calibrated according to portfolio breadth and scope of influence.
- Opportunity to work across product, engineering, clinical, regulatory, quality, and commercial functions.
- Cash bonus and equity in addition to base compensation.
- Equal-opportunity workplace committed to respect and non-discrimination.
Hiring process
- Level calibration takes place during the interview process based on demonstrated scope of influence and depth.
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