Product Manager

Posted 15 Days Ago
Santa Clara, CA, USA
In-Office
135K-155K Annually
Mid level
Hardware • Healthtech • Manufacturing
The Role
Own end-to-end product management for a multi-component cardiac device platform: gather VOC, prioritize R&D, build TAM, lead go-to-market and launches, manage SKU lifecycle and sales enablement, ensure regulatory and quality compliance, and coordinate cross-functional stakeholders to support commercial ramp and sustaining operations.
Summary Generated by Built In

Description

About EBR Systems

At EBR Systems, we're not imagining the future of cardiac care. We're building it. We are the team behind the world's first FDA-approved leadless left ventricular endocardial pacing device for heart failure. It's a breakthrough that's redefining what's possible, and it's just the beginning.

Based in Silicon Valley, we're advancing the WiSE System, a first-of-its-kind device in cardiac rhythm management. Your work here has a direct line to patients whose lives depend on what we build. We hire people who want to solve hard problems and who care about getting it right.

We invest in our people as much as our technology. Expect a collaborative, transparent culture, real career growth in a fast-moving startup, competitive compensation, equity, comprehensive benefits, and generous PTO.

If you want your work to matter, EBR is where you belong.

The Opportunity

This is a full-lifecycle Product Manager role and a foundational hire for our growing Marketing team. This is an onsite role at our Santa Clara office, with the ability to work from home 2 days per week.  The WiSE CRT System is a multi-component platform supported by an active R&D portfolio and an ambitious commercial ramp. You will own product management responsibilities spanning upstream needs-finding and roadmap through downstream launch execution and sustaining operations, partnering across R&D, Regulatory, Quality, Clinical, Operations, Sales, and Training. If you want end-to-end ownership and direct proximity to physicians and the technology, this role offers unusual breadth. 

ESSENTIAL AND OTHER DUTIES AND RESPONSABILITIES:

Essential Duties and Responsibilities

  

Upstream Product Management

  • Collect Voice of Customer inputs to help prioritize R&D projects and develop marketing requirements documents (MRDs).
  • Lead ongoing market & competitive analysis
  • Build and maintain the total addressable market (TAM) model; refine it as clinical and market data mature.
  • Channel user and field feedback into Leadership reviews on post-market surveillance

Downstream Product Management & Launch

  • Lead go-to-market planning and new product launches — launch strategy, cross-functional coordination, forecasting and availability, and physician and sales training hand-off.
  • Own product positioning, value propositions, and core messaging, tailored to key customer and stakeholder segments.
  • Develop and maintain the product claims matrix, partnering with Clinical and Regulatory to align claims with its supporting evidence and approved language.
  • Build sales enablement tools and training — playbooks, pitch decks, objection-handling and in-service guides, clinical-evidence talking points, and case libraries — in partnership with Sales, Training, and Clinical.
  • Provide product-related content for marketing assets (brochures, presentations, digital assets, product animations, trade-show materials) to Marketing Communications and creative partners.
  • Manage product transitions in the field, including component end-of-life, inventory swaps, and equipment upgrades.

Commercial Operations & Sustaining

  • Own SKU lifecycle management — creation, specification, configuration, discontinuation, and maintenance across all products and accessories.
  • Define demo/non-sterile product requirements for in-service, Training, and marketing/sales activities.
  • Set up e-fulfillment for promotional & demonstration items for the field

Cross-Functional Leadership & Compliance

  • Facilitate needs from the Commercial organization (Sales, Training, Marketing) across internal EBR teams in R&D, Regulatory, Quality, Clinical, Operations/Supply Chain.
  • Operate within the design-control and quality-management-system framework; maintain audit-ready documentation and reasoning.

Other Duties and Responsibilities

  • Other duties as assigned. 

 SUPERVISORY RESPONSABILITIES:

  • None

QUALIFICATIONS:

     

Education and Required Experience:

  •  Bachelor's degree in engineering, life   sciences, business, or a related field.
  • 3–6 years of product management experience   in medical devices, with demonstrated ownership across the product lifecycle   — from upstream needs-finding through commercial launch.
  • Direct experience leading or materially   supporting a product launch (NPI) in a cross-functional environment.
  • Experience with SKU lifecycle management.
  • Experience with promotional material and   sales tool development.
  • Can be an equivalent combination of   education and professional experience.

Knowledge, Skills, and Abilities:

  • Working knowledge of VOC / needs-finding methods and the ability to translate customer insight into requirements.
  • Strong analytical skills, including Excel and comfort working with CRM systems (e.g., Salesforce), and Microsoft Office.
  • Familiarity with design controls, quality-management systems, and the regulatory constraints governing device   labeling and claims.
  • Excellent written and verbal communication, including executive-ready deliverables.
  • Comfort operating in a fast-paced, small-cap medical device environment; able to work on-site in Santa Clara, CA and   travel to clinical cases and conferences.

Preferred

  • Master’s in Business Administration (MBA)
  • Experience in cardiac rhythm management, electrophysiology, cardiac resynchronization, or structural heart.
  • Experience launching Class III or active implantable devices and working with clinicians.

Physical Requirements

  • Required to stand, walk and sit; talk or   hear; use hands to finger, handle or feel objects or controls; reach with   hands and arms. 
  • Required to stoop, kneel, bend, crouch and   lift up to 20 pounds. 
  • Specific vision abilities required by this   job include close vision, distance vision, depth perception, color vision and   the ability to adjust focus.
  • Subject to extended periods of sitting   and/or standing, vision to monitor, and moderate noise levels.
Compensation & Benefits
  • Salary Range: $135,000 – $155,000.
  • Additional Compensation: Eligible for an annual performance bonus and equity/stock options.
  • Comprehensive medical, dental, and vision benefits (employee only covered at 100%)
  • 401k program with match
  • Generous PTO
  • Education stipend
  • A company-wide mandate to hire fast and hire well - recruiting is a business priority, not a back-office function here
  • A mission that matters:  Giving life-saving technology to patients with no other options

EBR Systems, Inc. is an Equal Opportunity Employer committed to a diverse, inclusive, and equitable workplace

EBR Systems, Inc. does not accept unsolicited resumes from headhunters, recruitment agencies, or fee-based recruitment services. Please refrain from solicitations at this time.

Skills Required

  • Bachelor's degree in engineering, life sciences, business, or related field (or equivalent experience)
  • 3-6 years product management experience in medical devices with full product lifecycle ownership
  • Direct experience leading or materially supporting a product launch (NPI) in a cross-functional environment
  • Experience with SKU lifecycle management
  • Experience developing promotional materials and sales enablement tools
  • Working knowledge of VOC / needs-finding methods and translating customer insight into requirements
  • Strong analytical skills, including Excel and comfort working with CRM systems (e.g., Salesforce) and Microsoft Office
  • Familiarity with design controls, quality-management systems, and regulatory constraints on device labeling and claims
  • Excellent written and verbal communication, including executive-ready deliverables
  • Ability to work onsite in Santa Clara, CA and travel to clinical cases and conferences
  • Ability to perform physical tasks listed (stand, walk, sit, lift up to 20 pounds, required vision abilities)
  • Master's in Business Administration (MBA)
  • Experience in cardiac rhythm management, electrophysiology, cardiac resynchronization, or structural heart
  • Experience launching Class III or active implantable devices and working with clinicians
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The Company
159 Employees
Year Founded: 2003

What We Do

EBR Systems, Inc. develops the WiSE System — a leadless left-ventricular endocardial pacing device for cardiac resynchronization therapy (CRT). Founded in 2003 and headquartered in Sunnyvale, CA, the company designs implantable wireless cardiac stimulation hardware to overcome limitations of conventional CRT and expand cardiac rhythm management options; it is commercializing the WiSE platform following regulatory approvals.

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