On-Site Production Lead — Medical Devices & Quality

iRhythm Technologies, Inc.; Anaheim (CA); On-site; USD 70,000 - 88,000; Full time

Job summary

iRhythm Technologies, Inc. in Orange County, California, is seeking a Production Supervisor to lead day‑to‑day manufacturing operations, ensure schedules are met safely and in compliance with quality and regulatory standards, and drive continuous improvement.

You will supervise teams, deliver training on GMP and GDP, coordinate with planning and supply chain, and uphold FDA and ISO 13485 requirements while maintaining documentation and performance metrics.

Qualifications

• Associate degree or equivalent experience in manufacturing.
• 3-5 years of experience in manufacturing operations, with 1-2 years in a supervisory role.
• Experience in a medical device or regulated industry.

Responsibilities

• Supervise daily production operations to meet output safely and to quality specifications.
• Maintain compliance with FDA, ISO 13485, and other medical device regulations.
• Communicate daily goals and performance expectations to the production team.
• Identify and upscale production issues to minimize schedule disruption.
• Lead and motivate associates to achieve performance goals.
• Train on SOPs, GDP, GMP, and ensure adherence to quality procedures.
• Coordinate with planning and supply chain to ensure material availability.
• Document production records, deviations, and maintenance activities.

Skills

Leadership

Communication

Problem-solving

Organizational skills

Team motivation

Education

Associate degree or equivalent

Bachelor's degree in Engineering/Manufacturing

Tools

ERP systems (QAD, SAP, Oracle)

Job description

iRhythm Technologies, Inc. in Orange County, California, is seeking a Production Supervisor to lead day‑to‑day manufacturing operations, ensure schedules are met safely and in compliance with quality and regulatory standards, and drive continuous improvement.

You will supervise teams, deliver training on GMP and GDP, coordinate with planning and supply chain, and uphold FDA and ISO 13485 requirements while maintaining documentation and performance metrics.