Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Средняя
$140к-165к/год
$120к$140кмедиана$170к
По похожим ролям (50) ~ $140к/год
На СНГ рынке: $3.1к/мес ($2.5к - $3.7к)
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Чёткая ответственность за портфель медицинских устройств, зарплата на уровне рынка и значимая задача в медтехе делают вакансию сильной, хотя гибридный формат и поездки подойдут не всем.
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Частые поездкиЧёткая зона ответственностиЗарплата на уровне рынкаМедтех с общественной пользой
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Product Manager (Medical Devices) (Hardware/Firmware): Managing FDA-regulated medical device products across development, launch, and sustaining with an accent on product requirements, design controls, usability, and cross-functional execution. Focus on driving hardware and firmware roadmaps, leading new product introductions, translating customer insights into product decisions, and ensuring compliance with clinical and quality standards.
Location: Hybrid in San Mateo, California, three days per week; local candidates only. Travel up to 25% of the time. Applicants must be authorized to work in the United States or eligible for work authorization through a sponsorship path hirify.global can support.
Salary: $140,000–$165,000 per year
Company
hirify.global develops non-invasive prescription therapies and connected medical devices for chronic disease, including neurology and cardiology applications.
What you will do
Own the physical device hardware and firmware portfolio across development, launch, sustaining, and end-of-life.
Drive product roadmap execution and align product priorities with portfolio strategy and business objectives.
Translate user, customer, and stakeholder needs into product requirements and documentation.
Lead new product introductions, launch planning, cross-functional readiness, and performance tracking.
Partner with Engineering, Quality, Regulatory, Clinical, Operations, and Commercial teams to deliver compliant products.
Collect Voice-of-the-Customer feedback and use market insights, data, and metrics to guide product decisions.
Requirements
3–5 years of experience in FDA-regulated medical devices.
Experience managing hardware-based products through development, launch, and post-market improvements.
Expertise in Design Controls, requirements management, Human Factors Engineering, and usability studies.
Strong Voice-of-the-Customer research, analytical, and market insight generation skills.
Experience leading cross-functional teams and balancing multiple priorities in a fast-paced environment.
Clear, structured communication and consensus-building skills.
Nice to have
Durable Medical Equipment experience.
Experience with wearable, software-enabled, or connected medical devices.
Culture & Benefits
Tools, training, and mentoring are provided to support employee development.
Work with cross-functional teams across Engineering, Clinical, Quality, Regulatory, Operations, and Commercial functions.
Product work is focused on reducing the burden of chronic disease through non-invasive medical technology.
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