Jobs at iRhythm Technologies

The Director of Procurement will lead procurement functions, drive savings, manage purchasing strategies, and develop supplier relationships to support business growth.

Leads electrical testing, failure analysis, root-cause investigations, test method development, process validation, and manufacturing support for regulated medical devices. Troubleshoots PCBAs and electronic assemblies, analyzes reliability and field data, supports CAPA and nonconformance investigations, drives corrective actions, and improves test automation, yield, quality, and product reliability. Collaborates with manufacturing, quality, suppliers, and design teams while ensuring FDA, ISO 13485, IEC 60601, and QMS compliance. Provides technical leadership and mentorship.

Designs, programs, integrates, troubleshoots, and maintains industrial automation systems for manufacturing assembly and packaging. Responsibilities include PLC control logic, industrial networking, HMI and SCADA development, system commissioning, root cause analysis, cybersecurity, MES/ERP integration, documentation, operator training, and preventive maintenance support. Collaborates with mechanical, electrical, IT, and production teams while ensuring safety and regulatory compliance.

The Senior Financial Analyst will support operations FP&A through budgeting, forecasting, financial reporting, variance analysis, ROI modeling, expense management, and monthly close activities. The role partners with operations, supply chain, cost accounting, and senior business leaders to deliver insights, track performance, support strategic projects, and manage financial risks and opportunities. This hybrid position requires 2–3 days onsite in Orange County.

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.

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