10 дней назад
Product Manager (Medical Devices)
140 000 - 165 000$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Product Manager (FDA-Regulated Medical Devices): Owning the lifecycle of physical medical device hardware and firmware products from new product development through launch and sustaining with an accent on product requirements, usability, clinical compliance, and cross-functional execution. Focus on driving hardware and firmware roadmaps, leading new product introductions, translating voice-of-customer insights into decisions, and managing post-market improvements.
Location: Hybrid in San Mateo, California, three days per week; local candidates only. Travel of up to 25% may be required.
Salary: $140,000–$165,000 per year.
Company
Develops non-invasive prescription therapies and connected medical devices for chronic diseases, including neurology and cardiology applications.
What you will do
- Own the physical device hardware and firmware portfolio across new product development, launch, sustaining, and end-of-life.
- Drive product roadmap execution and align product work with portfolio strategy and business priorities.
- 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 usability feedback and market insights, use product metrics, and manage improvements, cost reductions, and issue resolution.
Requirements
- 3–5 years of experience specifically in FDA-regulated medical devices.
- Experience managing hardware-based products from development and launch through post-market improvements.
- Expertise in Design Controls, requirements management, Human Factors Engineering, and usability studies.
- Strong voice-of-customer research, insight generation, analytical, and data-driven decision-making skills.
- Proven ability to lead cross-functional teams, balance multiple priorities, and build consensus.
- Must be authorized to work in the United States full-time, or eligible for a sponsorship path supported by the company.
Nice to have
- Durable Medical Equipment experience.
- Experience with wearable medical devices and software-enabled or connected devices.
Culture & Benefits
- Tools, training, and mentoring are provided to support employee development.
- Work involves close collaboration across engineering, clinical, quality, regulatory, operations, and commercial functions.
- Product work is focused on reducing the burden of chronic disease through non-invasive therapies.
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