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.

The role involves testing embedded systems software and desktop applications, defining testing strategies, developing protocols, and ensuring quality adherence in regulated environments.

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 Quality Control Manager leads inspection and compliance activities in manufacturing, ensuring product quality and regulatory adherence. They oversee QC teams, drive continuous improvement initiatives, and manage nonconformance processes to enhance operational efficiency.

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