iRhythm Technologies, Inc.
Supervisor, Production (2nd Shift | 3pm - 11pm PST)
iRhythm Technologies, Inc., California, Missouri, United States, 65018
Supervisor, Production (2nd Shift | 3pm – 11pm PST)
This day-to-day supervisor role manages iRhythm’s manufacturing operations for a 2nd shift production line. The role ensures production schedules are met safely, efficiently, and in compliance with all quality and regulatory standards. Base Pay
USD 68,000 – 85,000 per year (actual compensation may vary). Location
Orange County, California. Key Responsibilities
Supervise daily production operations to deliver quality products on time. Maintain compliance with FDA, ISO 13485, and other medical device regulations. Communicate daily goals, priorities, and performance expectations to the manufacturing team. Identify and escalates production issues promptly. Lead and motivate manufacturing associates; conduct training and coaching. Monitor attendance, performance, safety, and quality procedures. Execute production plans, adjust staffing/resources to meet output requirements. Document production records, deviations, and maintenance activities. Partner with planning and supply chain to optimize materials and inventory. Monitor Plan vs. Actual performance and root cause analysis. Support nonconformance investigations, CAPAs, and quality audits. Promote adherence to Good Documentation Practices and data integrity. Maintain safe and compliant work environment; conduct safety inspections. Participate in continuous improvement initiatives (Lean, 5S). Qualifications
Associate degree required; Bachelor’s degree in Engineering, Manufacturing or related field preferred. 3–5 years of experience in manufacturing operations; 1–2 years in a supervisory role, preferably in a regulated or medical device environment. Experience leading small to medium production teams. Knowledge of ISO 13485, FDA 21 CFR Part 820, GMP, and quality systems. Familiarity with ERP or MRP systems (e.g., QAD, SAP, Oracle). Strong communication, problem‑solving, organizational, and leadership skills. Commitment to teamwork, employee engagement, and continuous improvement. Work Environment
On‑site production floor; may involve shift and weekend coverage; occasional overtime may be required. FSLA Status
Exempt. Equal Employment Opportunity
iRhythm Technologies, Inc. is an Equal Opportunity Employer (M/F/V/D). Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment all qualified applicants with arrest and conviction records. Accommodations
We welcome and celebrate people of all backgrounds, experiences, skills, and perspectives. iRhythm provides reasonable accommodations for qualified individuals with disabilities in job application procedures. If you need an accommodation, you may contact us at taops@irhythmtech.com.
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This day-to-day supervisor role manages iRhythm’s manufacturing operations for a 2nd shift production line. The role ensures production schedules are met safely, efficiently, and in compliance with all quality and regulatory standards. Base Pay
USD 68,000 – 85,000 per year (actual compensation may vary). Location
Orange County, California. Key Responsibilities
Supervise daily production operations to deliver quality products on time. Maintain compliance with FDA, ISO 13485, and other medical device regulations. Communicate daily goals, priorities, and performance expectations to the manufacturing team. Identify and escalates production issues promptly. Lead and motivate manufacturing associates; conduct training and coaching. Monitor attendance, performance, safety, and quality procedures. Execute production plans, adjust staffing/resources to meet output requirements. Document production records, deviations, and maintenance activities. Partner with planning and supply chain to optimize materials and inventory. Monitor Plan vs. Actual performance and root cause analysis. Support nonconformance investigations, CAPAs, and quality audits. Promote adherence to Good Documentation Practices and data integrity. Maintain safe and compliant work environment; conduct safety inspections. Participate in continuous improvement initiatives (Lean, 5S). Qualifications
Associate degree required; Bachelor’s degree in Engineering, Manufacturing or related field preferred. 3–5 years of experience in manufacturing operations; 1–2 years in a supervisory role, preferably in a regulated or medical device environment. Experience leading small to medium production teams. Knowledge of ISO 13485, FDA 21 CFR Part 820, GMP, and quality systems. Familiarity with ERP or MRP systems (e.g., QAD, SAP, Oracle). Strong communication, problem‑solving, organizational, and leadership skills. Commitment to teamwork, employee engagement, and continuous improvement. Work Environment
On‑site production floor; may involve shift and weekend coverage; occasional overtime may be required. FSLA Status
Exempt. Equal Employment Opportunity
iRhythm Technologies, Inc. is an Equal Opportunity Employer (M/F/V/D). Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment all qualified applicants with arrest and conviction records. Accommodations
We welcome and celebrate people of all backgrounds, experiences, skills, and perspectives. iRhythm provides reasonable accommodations for qualified individuals with disabilities in job application procedures. If you need an accommodation, you may contact us at taops@irhythmtech.com.
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