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3 дня назад

Principal/Director, Product Management (AI MedTech)

240 000 - 295 000$
Тип работы
fulltime
Грейд
senior/director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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

hirify.global 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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