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1 день назад

Senior Technical Product Manager (Medical Software)

145 000 - 180 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Senior Technical Product Manager (Medical Software): Leading delivery of complex GenXpert software capabilities across multiple teams with an accent on product scope, requirements management, backlog prioritization, and regulated medical-device development. Focus on integrating AI into Agile requirements workflows, maintaining traceability and verification-ready documentation, and managing release risks across Scrum teams.

Location: Onsite in Sunnyvale, California, United States. Travel of up to 15% domestically and internationally is required.

Annual salary: $145,000–$180,000 USD, plus eligibility for bonus or incentive pay.

Company

hirify.global operates Cepheid, a life sciences and molecular diagnostics company developing fast, accurate diagnostic systems and tests.

What you will do

  • Define and manage software product scope on quarterly and annual horizons in line with long-term strategy.
  • Lead delivery of complex GenXpert software capabilities across Software, Hardware, Assay, Operations, and other stakeholder groups.
  • Use AI in problem framing, functional decomposition, story mapping, acceptance-criteria drafting, and requirements documentation.
  • Author and maintain technical epics, user stories, and acceptance criteria in JIRA and Confluence.
  • Own and prioritize the product backlog across multiple Scrum teams, leading sprint execution and release planning.
  • Track engineering release metrics and use data analytics to manage dependencies, risks, impediments, and delivery decisions.

Requirements

  • Bachelor’s or master’s degree in computer science or a related field.
  • 8+ years of experience as a Software Product Owner or Business Analyst in regulated medical device or IVD environments.
  • 5+ years of experience with Agile and SDLC practices, including backlog management in JIRA and documentation in Confluence.
  • Experience delivering software in FDA-, ISO 13485-, or IVDR-compliant environments.
  • Strong background in requirements management, traceability, and lifecycle documentation aligned with IEC 62304 or equivalent standards.
  • Ability to work onsite in Sunnyvale and travel up to 15%.

Nice to have

  • Hands-on experience using AI assistants for functional requirements, acceptance criteria, ambiguity detection, and edge-case identification.
  • Experience working with globally distributed teams and developing software products in regulated environments.

Culture & Benefits

  • Work within a culture focused on belonging, continuous improvement, and measurable impact in healthcare.
  • Comprehensive benefits package including paid time off.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) benefits for eligible employees.
  • Bonus or incentive pay eligibility.

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