New · posted Oct 15
iRhythm · Medical Devices
Quality Control Manager
- Orange County, CA
- On-site
- Full-time
- Manager
Open until filled
The role
Career-defining. Life-changing.
At iRhythm, you’ll have the opportunity to grow your skills and your career while impacting the lives of people around the world. iRhythm is shaping a future where everyone, everywhere can access the best possible cardiac health solutions. Every day, we collaborate, create, and constantly reimagine what’s possible. We think big and move fast, driven by our commitment to put patients first and improve lives. We need builders like you. Curious and innovative problem solvers looking for the chance to meaningfully shape the future of cardiac health, our company, and your career
The Quality Control Manager is responsible for leading Quality Control execution across Manufacturing and Receiving operations, ensuring effective inspection, documentation, material control, and disposition activities. This role provides direct leadership to Manufacturing Quality Inspectors and Receiving Inspection teams and owns day-to-day quality control execution on the manufacturing floor.
The Quality Control Manager ensures compliance with applicable regulatory requirements and internal procedures while enabling efficient production through robust inspection plans, effective nonconformance and deviation management, and continuous improvement initiatives.
What you need
What you'll do
1. Quality Control Leadership & Execution
- Lead, coach, and develop Manufacturing Quality Inspectors and Receiving Inspection personnel.
- Ensure inspectors are trained, qualified to perform inspections and documentation per approved procedures.
- Establish clear expectations and accountability for inspection accuracy, documentation integrity, and timely escalation of quality issues.
2. Inspection Strategy & Manufacturing Quality Support
- Support the development, implementation, and continuous improvement of inspection plans, sampling strategies, and control plans in collaboration with Quality Engineering, Supplier Quality and Manufacturing Engineering.
- Ensure effective in-process, final, and receiving inspections are executed in accordance with approved inspection plans and work instructions.
- Drive improvements to inspection efficiency, first-pass yield, and defect containment across manufacturing operations.
3. Nonconformance, MRB & Planned Deviation Support
- Ensure timely identification, documentation, and containment of nonconforming material in manufacturing and receiving.
- Support and participate in Material Review Board (MRB) activities, ensuring accurate disposition execution and documentation.
- Support planned deviations to maintain production continuity while ensuring risk assessments, approvals, and documentation are completed per the Quality Management System.
- Ensure all dispositions, deviations, and containment actions are accurately reflected in work orders, travelers, and batch records.
4. Material Identification, Traceability & Documentation Control
- Ensure proper material identification, segregation, labeling, and traceability from receiving through manufacturing and final disposition.
- Enforce Good Documentation Practices (GDP) across inspection records, batch records, travelers, RI/DAI records, and disposition documentation.
- Ensure work orders, travelers, and batch records are executed in compliance with approved procedures and instructions.
Batch Record Review
- Own the review, verification, and acceptance of manufacturing batch records and travelers to ensure completeness, accuracy, and compliance prior to lot release or handoff.
- Verify that all required inspection results, testing reports, in-process checks, deviations, nonconformances, and MRB dispositions are properly documented and approved within the batch record or traveler.
- Ensure traceability is complete and intact, including material lots, subassemblies, equipment identification, and inspection status.
- Identify documentation errors, omissions, or trends during batch record review and ensure timely correction, escalation, and retraining as necessary.
- Partner with Manufacturing and Quality Engineering to improve batch record clarity, usability, and execution robustness.
5. Receiving Inspection Oversight
- Oversee execution of Receiving Inspection and FAI activities per approved sampling plans and inspection criteria.
- Ensure accuracy, completeness, and traceability of RI and FAI records, including lot identification and acceptance status.
- Collaborate with Supplier Quality to ensure timely escalation and documentation of supplier-related quality issues.
6. Equipment Control: Calibration, PM & Maintenance Support
- Support of calibration and preventive maintenance (PM) programs for inspection and manufacturing equipment used for product acceptance.
- Ensure equipment is calibrated, maintained, and suitable for its intended use prior to release for production or inspection.
- Support corrective maintenance activities by ensuring quality impact assessments are completed, documentation is updated, and effectiveness is verified following repairs or failures.
7. Compliance, Audit Support & Risk Management
- Ensure QC operations comply with ISO 13485, QSMR/FDA 21 CFR 820 and applicable internal SOPs, DOP’s and work instructions.
- Support internal audits, external audits, and regulatory inspections by demonstrating effective QC execution and control.
- Monitor QC-related metrics and trends to proactively identify compliance risks and improvement opportunities.
8. Continuous Improvement & Gemba Leadership
- Own continuous improvement initiatives within Quality Control, including monthly Gemba walks focused on inspection effectiveness, material flow, documentation quality, and compliance.
- Use data, observations, and team feedback to identify systemic gaps and drive sustainable improvements.
- Partner with cross-functional teams to implement corrective and preventive improvements.
What We Want to See
- Bachelor’s Degree in Life Sciences, Engineering, or a related technical discipline is required; Master’s Degree is preferred.
- Minimum of 8 years of progressive experience in a medical device manufacturing environment, with demonstrated responsibility for quality control, inspection, or manufacturing quality operations.
- Strong working knowledge of ISO 13485, FDA 21 CFR Parts 820 , with working familiarity of EU MDD and EU MDR requirements.
- Demonstrated ability to identify, investigate, and resolve complex quality and manufacturing issues, including nonconformances, MRB activities, deviations, and corrective actions.
- Proven experience collaborating with Manufacturing, Quality Engineering, Supplier Quality, Engineering, Operations, and Facilities/Maintenance teams.
- High level of attention to detail, with strong focus on timeliness, data accuracy, and GDP compliance.
- Excellent verbal and written communication skills, with the ability to communicate expectations, risks, and decisions at all organizational levels.
- Working knowledge of statistical and quality tools, including trend analysis, process capability (Cp/Cpk, Pp/Ppk), Gage R&R, and defect trend analysis.
- Working knowledge of medical device risk management, including process FMEAs and alignment with ISO 14971 principles.
Ways to Stand Out
- Highly organized, with the ability to manage multiple priorities, balance production demands with compliance, and operate effectively in a fast-paced manufacturing environment.
- Demonstrated leadership style that is empathetic, collaborative, and accountability-driven, with experience coaching and developing QC inspectors and quality personnel.
- Experience providing training, mentoring, and development to strengthen inspection capability and consistency.
Pay
$112,000 – $145,000 a year
Employer providedEstimated Pay Range
$112,000.00 - $145,000.00
Where you'll work
Orange County, CAOn-siteOpen in Maps (opens in a new tab)
More jobs in Orange County, CAWorking conditions
Location
Orange County
Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location.
From the posting
About iRhythm
Why This Role Is Critical
- Establishes clear ownership of shop-floor quality execution
- Reduces compliance and audit risk related to inspection, documentation, and material control
- Enables scalable manufacturing growth while maintaining product quality and regulatory compliance
- Strengthens quality culture through visible leadership and continuous improvement
About iRhythm Technologies
iRhythm is a leading digital healthcare company that creates trusted solutions that detect, predict, and prevent disease. Combining wearable biosensors and cloud-based data analytics with powerful proprietary algorithms, iRhythm distills data from millions of heartbeats into clinically actionable information. Through a relentless focus on patient care, iRhythm’s vision is to deliver better data, better insights, and better health for all.
Make iRhythm your path forward. Zio, the heart monitor that changed the game.
There have been instances where individuals not associated with iRhythm have impersonated iRhythm employees pretending to be involved in the iRhythm recruiting process, or created postings for positions that do not exist. Please note that all open positions will always be shown here on the iRhythm Careers page, and all communications regarding the application, interview and hiring process will come from a @irhythmtech.com email address. Please check any communications to be sure they come directly from @irhythmtech.com email address. If you believe you have been the victim of an imposter or want to confirm that the person you are communicating with is legitimate, please contact [email protected]. Written offers of employment will be extended in a formal offer letter from an @irhythmtech.com email address ONLY.
For more information, see https://www.ftc.gov/business-guidance/blog/2023/01/taking-ploy-out-employment-scams and https://www.ic3.gov/Media/Y2020/PSA200121
Equal opportunity, accessibility and legal noticesiRhythm's statements, word for word
As a part of our core values, we ensure an inclusive workforce. We welcome and celebrate people of all backgrounds, experiences, skills, and perspectives. iRhythm Technologies, Inc. is an Equal Opportunity Employer. We will consider for employment all qualified applicants with arrest and conviction records in accordance with all applicable laws.
iRhythm provides reasonable accommodations for qualified individuals with disabilities in job application procedures, including those who may have any difficulty using our online system. If you need such an accommodation, you may contact us at [email protected]
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is 1% above the US median for Quality Control roles at this level.
This roleEmployer provided
Manager roles in California5 roles publishing pay
Manager roles in the US24 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $112,000 | — | $145,000 |
| California (middle half) | $128,500 | $140,000 | $171,000 |
| All US (middle half) | $108,500 | $127,250 | $143,500 |
This role: iRhythm's own published range. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 275 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not iRhythm's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 46 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance25
- Documentation and SOPs19
- Collaboration and leadership12
- Quality systems and risk9
- Investigations and CAPA6
- Regulatory submissions2
- Lab testing and methods1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices
- European UnionEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Risk management for medical devices
Company hiring pulse
iRhythm on Regulatory Jobs
- 6
- Open roles
- 6
- Distinct roles
- 3
- Locations
By discipline
- Quality5 83%
- Regulatory1 17%
By level
- Manager2 33%
- Senior & Principal2 33%
- Director1 17%
More roles at iRhythm
- View role
Firmware Quality Assurance Engineer Co-Op Intern
San Francisco, CAAssociate & SpecialistMedical Devices$52K–$73K
- View role
Senior Supplier Quality Engineer
Orange County, CA · HybridSenior & PrincipalMedical Devices$99K–$129K
- View role
Director, Design Quality
Remote, USDirectorMedical Devices$182K–$237K
- View role
Senior Design Quality Engineer
San Francisco, CA +1 more · HybridSenior & PrincipalMedical Devices$138K–$180K
Similar Quality Control roles elsewhere
- View role
Manager Quality Control
TransMedicsAndover, MAManagerMedical Devices$119K–$148K
- View role
Quality Control Manager
The Cretex CompaniesBrooklyn Park, MNManagerMedical Devices$101K–$151K
- View role
QC Lab Supervisor
STERISSt. Louis, MOManagerMedical Devices$80K–$103K
- View role
Senior Quality Manager
BaxterCleveland, MSManagerMedical Devices$136K–$170K
Quality Control Manager at iRhythm
Open until filled. $112K–$145K a year, employer provided.