Eko Health, Inc.
(Eko) is a leading digital health company advancing how healthcare professionals detect and monitor heart and lung disease with its portfolio of digital stethoscopes and AI detection platform, SENSORA™.
The company’s FDA-cleared technologies are used by hundreds of thousands of healthcare professionals worldwide, allowing them to detect earlier and with higher accuracy, diagnose with more confidence, manage treatment effectively, and ultimately give their patients the best care possible.
Eko Health is headquartered in Emeryville, California, with over $125 million in funding from Highland Capital Partners, Questa Capital, Artis Ventures, DigiTx Partners, NTTVC, Morningside Technology Ventures Limited, Mayo Clinic, Sutter Health, and others.

Eko Health

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compliance

Eko Health is a company specializing in digital and AI-powered stethoscopes and health solutions. Their products, such as the Eko CORE 500™ and Eko DUO, integrate digital stethoscope technology with artificial intelligence to enhance the detection of cardiovascular diseases, including murmurs, atrial fibrillation, and heart failure. Eko's technology is utilized in telehealth settings, life sciences partnerships, and for health systems globally, providing enhanced clinical insights through acoustic and cardiac examination tools. Their solutions aim to improve the standard of care by providing better diagnostic insights during auscultation, supporting clinicians in making more accurate and confident health assessments.

Eko Health, Inc. (Eko) is a leading digital health company advancing how healthcare professionals detect and monitor heart and lung disease with its portfolio of digital stethoscopes and AI detection platform, SENSORA™. The company’s FDA-cleared technologies are used by hundreds of thousands of healthcare professionals worldwide, allowing them to detect earlier and with higher accuracy, diagnose with more confidence, manage treatment effectively, and ultimately give their patients the best care possible. Eko Health is headquartered in Emeryville, California, with over $125 million in funding from Highland Capital Partners, Questa Capital, Artis Ventures, DigiTx Partners, NTTVC, Morningside Technology Ventures Limited, Mayo Clinic, Sutter Health, and others.

• Proven ability to own and drive end-to-end regulatory strategy from concept through commercialization, including portfolio prioritization and resource allocation aligned with business goals
• Lead and execute regulatory submissions (FDA 510(k)/De Novo, CE Mark, Health Canada, PMDA) for medical device hardware and SaMD products, directly authoring technical documentation and managing agency interactions (e.g., interactive responses and presubmission meetings) to secure timely approvals
• Serve as the regulatory lead for the company, managing all interactions with regulatory authorities including pre-submissions, responses to deficiencies, inspections, and ongoing correspondence
• Partner with cross-functional teams (R&D, Clinical, Quality, Product, Commercial) to define and proactively embed regulatory requirements into product development workflows and align global market access strategies with business priorities
• Collaborate with Head of Quality to ensure the Quality Management System represents state-of-the-art practices and supports regulatory compliance and post-market surveillance programs
• Establish and lead a proactive regulatory intelligence program to monitor evolving global requirements (EU MDR, EU AI Act, FDA SaMD guidance, IMDRF standards), provide and implement strategic recommendations to executive leadership on product roadmap, risk mitigation, and competitive positioning
• Build and mentor a high-performing regulatory team while driving the continuous optimization of internal workflows and submission processes, establishing scalable processes that support rapid portfolio expansion while maintaining compliance excellence
• Ensure compliance with company policies and applicable laws across all regulatory activities, including adverse event reporting, clinical studies and evaluations, and labeling requirements
• Other duties as assigned

Director, Global Regulatory Affairs – Intelligence

Director of Global Regulatory Affairs leading regulatory strategy for AI medical devices in a dynamic healthcare company. Ensuring compliance and facilitating accelerated market access for innovative products.

marketing

• Own strategy, planning, and execution for all conferences and tradeshows.
• Partner with sales and leadership to build pre-event and post-event workflows (targeting lists, outreach cadences, booth messaging, event invites, lead follow-up).
• Manage conference assets including banners, booths, handouts, case studies, and video needs.
• Develop field-ready content and campaigns to support pipeline acceleration across our Enterprise business.
• Budget management for conferences and tradeshows
• Own organic social media strategy for enterprise channels (LinkedIn & X), including writing, scheduling, engagement monitoring, and performance tracking.
• Lead segmentation and targeting lists supporting strategic outbound and ABM programs.
• Build and optimize multi-touch email campaigns in marketing automation tools.
• Partner with Growth Marketing on paid campaigns and enterprise-specific audience targeting.
• Support the creation of key enterprise assets such as sales decks, 1-pagers, brochures, case studies, conference materials, and product marketing updates
• Collaborate with clinical, product, creative, and sales teams to ensure alignment, accuracy, and compliance.
• Manage inbound lead flow, qualification routing, and monthly reporting dashboards.
• Track funnel performance (MCL → MQL → Opportunity) for enterprise segments.
• Deliver insights that inform campaign strategy, targeting, and ROI.
• Support company awards submissions and industry recognition programs.

Enterprise Marketing Manager

Enterprise Marketing Manager leading enterprise-level marketing initiatives at a healthcare technology company. Overseeing demand generation and enhancing product adoption across health systems.

growth-marketing

• Lead and scale select B2C direct-to-consumer marketing channels, with an immediate focus on ROAS performance.  Will start with programmatic display/native as the primary channel of focus, with additional channels to be taken on in the future following business need and bandwidth
• Build and manage full-funnel acquisition strategies, through prospecting net new audiences and retargeting high-intent users, to grow incremental revenue at efficient ROAS
• Proactively own the full lifecycle of channel management: onboarding, research, planning, execution, creative strategy, tactical optimization, and reporting—with an innovative, test-and-learn mindset.
• Optimize channels by proactively improving targeting, creative strategy, testing velocity, bid strategies, landing page strategy, etc. to improve ROAS at scale
• Drive channels’ creative strategy and storytelling—developing clear, compelling narratives for each audience, based on channel-specific performance data and brainstormed new ideas
• Establish clear performance goals, KPIs, and tracking frameworks for each channel with a primary focus on ROAS and scalability.
• Present weekly performance updates, insights, and optimization recommendations to cross-functional stakeholders and leadership.
• Partner closely with creative, content, ecommerce, and analytics teams to develop compelling channel-specific messaging, assets, and customer journeys.
• Collaborate with BI and data teams to develop attribution frameworks, and reporting that drive decision-making.
• Stay ahead of marketing, platform, and creative trends to identify new opportunities that keep Eko competitive.

Growth Marketing Channel Manager

Growth Marketing Channel Manager scaling Eko's B2C direct-response acquisition channels focusing on programmatic and paid social marketing. Driving efficiency and revenue growth in a fast-paced digital health environment.

mechanical-engineer

• Design mechanical systems and enclosures using SolidWorks for advanced medical devices
• Create detailed drawings, assemblies, and manufacturing specifications
• Conduct tolerance analysis and design for manufacturability (DFM)
• Work closely with our supply chain and program management team to engage with contract manufacturers and component vendors globally
• Work with CMs to design and optimize manufacturing processes for scale production
• Lead design for assembly (DFA) and cost optimization initiatives
• Design and execute experimental protocols using Design of Experiments (DOE) methodology
• Develop test fixtures and validation procedures for medical device compliance
• Analyze statistical data to drive design decisions and process improvements
• Work closely with electronics teams on mechanical-electrical integration
• Collaborate with industrial designers on form factor and user experience
• Interface with firmware engineers on sensor mounting and signal optimization

Senior Mechanical Engineer

Senior Mechanical Engineer leading mechanical design and manufacturing of digital stethoscopes at Eko. Collaborating across teams to meet medical standards and consumer expectations in healthcare technology.

Eko Health

About the company

Open jobs

4 jobs found

Director, Global Regulatory Affairs – Intelligence

Eko Health

Enterprise Marketing Manager

Eko Health

Growth Marketing Channel Manager

Eko Health

Senior Mechanical Engineer

Eko Health