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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.

This role requires a Staff Firmware Engineer to lead firmware projects for medical devices, focusing on architecture, implementation, and cybersecurity decisions in a regulated environment.

Oversee a team of engineers while managing the technical strategy for web-based applications in a regulated medical device environment.

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.

This role involves optimizing HR processes through the configuration and maintenance of Workday, focusing on Benefits and Absence management, and providing support for HR business needs.

Designs, builds, and supports corporate networks, servers, storage, telephony, and cloud systems across on-prem, colo, and cloud. Leads infrastructure projects, provides technical escalation, mentors staff, manages vendors, drives vulnerability remediation and lifecycle tasks, and supports global 24x7 operations with SOX compliance.

The Territory Manager will drive growth by acquiring new business and expanding iRhythm's market presence, focusing on the Zio platform in cardiology and electrophysiology.

Provide day-to-day administration and user support for Workday Adaptive Planning and related financial systems. Maintain models, reports, integrations, and security; validate data and reconcile between ERP and planning systems. Support planning cycles, system enhancements, UAT, training, and audit/compliance activities while collaborating with Finance, Accounting, IT, and vendors.

As a Senior Systems Engineer II for ECG Monitoring Applications, you will design software solutions for arrhythmia detection, manage system architecture, and ensure seamless integration while collaborating with cross-functional teams.

Lead the validation and compliance of non-product software used in medical device development. Responsibilities include defining validation strategies, ensuring compliance with FDA and ISO standards, and cross-functional collaboration.