1 день назад
Senior Technical Product Manager (Medical Software)
145 000 - 180 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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