Jobs at iRhythm Technologies

Leads complex embedded hardware and firmware development projects from concept through production and commercialization. Owns project planning, schedules, resources, risks, documentation, design-control release plans, and cross-functional execution. Acts as scrum master, facilitates technical discussions, coordinates engineering, quality, regulatory, manufacturing, clinical, and commercial teams, and ensures compliance with company and international standards. Supports production release, project health monitoring, and continuous process improvement for medical device products.

Supports medical device product development from concept through commercialization and post-market evaluation. Leads design controls, risk management, verification and validation, design history files, traceability, risk assessments, change evaluations, technical reporting, and audit support. Partners with hardware, firmware, software, and engineering teams to ensure compliance with quality systems, medical device regulations, and standards including IEC 60601, IEC 62366, IEC 62304, ISO 13485, and ISO 14971.

The role involves managing a firmware team for cardiac monitoring devices, guiding technical decisions, collaborating cross-functionally, and ensuring compliance with engineering standards.

The Key Account Manager at iRhythm will nurture relationships with high-volume accounts, ensure customer satisfaction, monitor account performance, and collaborate internally to drive business success.

The manager will develop regulatory strategies for medical devices, manage a regulatory team, lead FDA submissions, and ensure compliance with global regulations.

Field-based Territory Manager responsible for new business development, strategic selling to cardiology/EP stakeholders, full sales-cycle management, territory planning and pipeline forecasting, cross-functional account management, and meeting quarterly/annual sales targets while traveling extensively within a defined geographic territory.

Drive sales growth for the Zio cardiac monitoring platform across Central LA by acquiring new healthcare accounts, expanding market share, and managing the full sales cycle. Build relationships with cardiologists, electrophysiologists, health systems, and executives; deliver value-based presentations; manage territory pipelines in Salesforce; oversee account adoption, training, inventory, and workflow optimization; analyze market performance; and collaborate cross-functionally to achieve sales targets.

Lead technical ownership of the Gateway Android app for a safety-critical mobile cardiac telemetry product. Architect and implement reliable long-running Android applications, make architectural decisions, write production code, drive design discussions and code reviews, mentor engineers, and establish durable engineering practices. Collaborate with cross-functional teams and ensure robust BLE, background execution, and secure communication capabilities.

Leads technical medical device projects from planning through launch and post-implementation. Responsibilities include project scoping, scheduling, budgeting, risk management, design-control release planning, Scrum facilitation, cross-functional coordination, technical discussions, testing support, regulatory compliance, production release monitoring, and process improvement.

The Senior Systems Engineer I will develop and enhance mobile applications for cardiac health solutions, collaborating with engineers and cross-functional teams to ensure compliance with standards and successful project delivery.

Leads finance support for cost-of-revenue functions, including manufacturing, cost accounting, clinical operations, quality, regulatory, and sales and operations planning. Owns budgeting, forecasting, long-range planning, gross-margin performance, cost controls, inventory accounting, integrations, and executive decision support. Builds scalable finance capabilities, improves processes and analytics, develops high-performing teams, and partners with operations and executive leadership on productivity, risk, and strategic growth.

Provides commercial legal counsel to commercial, market access, payer relations, and sales teams. Drafts and negotiates customer, payer, service, consignment, EHR integration, and strategic agreements. Advises on healthcare laws, fraud and abuse, compliance, billing, reimbursement, privacy, and transparency. Develops contract templates and negotiation processes, supports strategic transactions, conducts legal research, and translates legal developments into business guidance for medical device and digital health operations.

Drive adoption and market expansion of iRhythm’s Zio cardiac monitoring platform across Eastern Washington and Montana. Develop new healthcare business, manage the full sales cycle, build relationships with cardiologists, electrophysiologists, health systems, and executives, and execute strategic territory plans. Manage pipelines and forecasting in Salesforce.com, oversee account performance, training, inventory, and workflow optimization, analyze market trends, and consistently achieve sales targets while collaborating with cross-functional teams.

Leads the enterprise AI platform and transformation roadmap, moving generative AI from experimentation into secure, scalable production. Oversees AI architecture, LLM applications, RAG, agents, data integration, governance, reliability, monitoring, adoption, and value realization. Partners with executive, engineering, security, privacy, legal, compliance, quality, and finance teams while leading internal teams and strategic vendors. The role requires extensive experience building healthcare AI products and large-scale machine learning infrastructure in regulated environments.

Drives growth for iRhythm’s Zio cardiac monitoring platform across a defined territory. Responsibilities include acquiring new business, expanding healthcare-system adoption, managing the full sales cycle, building physician and executive relationships, developing territory plans, maintaining Salesforce pipeline forecasts, optimizing account performance, analyzing market trends, and meeting sales goals. The role requires extensive field travel and collaboration with clinical, payer, billing, customer success, and marketing teams.

Field-based Territory Manager responsible for expanding adoption of iRhythm’s Zio cardiac monitoring platform across South Connecticut. Duties include acquiring new healthcare accounts, managing the full sales cycle, developing territory growth plans, engaging cardiologists and health system stakeholders, managing pipelines in Salesforce, optimizing account performance, analyzing market trends, and meeting sales targets. Requires extensive territory travel and experience in medical device or healthcare technology sales.

The Territory Manager will drive adoption and revenue growth for iRhythm’s Zio cardiac monitoring platform across a defined territory. Responsibilities include acquiring new business, developing strategic sales plans, managing the full sales cycle, engaging cardiologists and healthcare executives, expanding health-system accounts, maintaining Salesforce pipeline data, supporting onboarding and account performance, analyzing market trends, and meeting sales targets. The role requires extensive field travel and collaboration with cross-functional teams.

Leads product discovery, roadmap prioritization, requirements definition, and delivery for clinician-facing digital workflow software. Partners with engineering, design, clinical, regulatory, operations, and commercial teams to launch scalable features, measure adoption and operational impact, and guide post-launch improvements. The role requires healthcare technology experience, strong stakeholder leadership, workflow and systems analysis, analytics proficiency, and familiarity with regulated software, integrations, and product management tools. Remote within the US, with travel up to 20%.

Lead execution and architecture for early-stage medtech innovations across AI, sensors, digital biomarkers, and wearables. Drive needs-finding, feasibility, business cases, partnerships, and transition of validated concepts into funded product development while aligning cross-functional stakeholders and managing portfolio timelines, budgets, and evidence strategies.

Lead scientific aspects of clinical research projects including study design, analysis, protocol development, evidence dissemination, and cross-functional collaboration to support device market clearance and post-market evidence. Drive analyses of prospective and real-world data, author regulatory and scientific documents, support HEOR and regulatory teams, and oversee project execution and quality standards.