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Material Control Manager Jobs in Irvine, CA (NOW HIRING)

Divergent

Inventory Control Manager

Long Beach, CA

... materials disposition, inventory movements, and labor or machine hours where applicable. * Monitor ... S05/Inventory Control Manager : $109,240 - $150,210 Pay Range $109,240--$150,210 USD What We Offer:

New

Divergent

Inventory Control Manager

Irvine, CA

... materials disposition, inventory movements, and labor or machine hours where applicable. * Monitor ... S05/Inventory Control Manager : $109,240 - $150,210 Pay Range $109,240--$150,210 USD What We Offer:

New

SIP Manufacturing, LLC

QC Technician

Lake Elsinore, CA · On-site

$18.25 - $23.50/hr

Quality Control Technician 2.- REPORTS TO: QC Manager 3.- BACK-UP BY: Another QC tech 4.- IMMEDIATE SUBORDINATE: none 5.- OBJECTIVE: Quality control technicians are responsible for testing materials ...

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All JobsMaterial Control JobsMaterial Control Manager JobsMaterial Control Manager Jobs in Irvine, CA

Material Control Manager information

See Irvine, CA salary details

$38.1K

$76.7K

$100.4K

How much do material control manager jobs pay per year?

As of Aug 23, 2026, the average yearly pay for material control manager in Irvine, CA is $76,716.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,000.00 and $90,200.00 per year, depending on experience, location, and employer.

What is a material control manager?

Material Control Managers are professionals responsible for overseeing the flow, storage, and distribution of materials within an organization. They ensure that materials needed for production or operations are available in the right quantities and at the right times, while minimizing excess inventory and controlling costs. Their duties often include inventory management, coordinating with suppliers, and implementing efficient processes for material handling to support business objectives.

What are the key skills and qualifications needed to thrive as a material control manager?

To thrive as a Material Control Manager, you need expertise in inventory management, supply chain logistics, and a bachelor's degree in business, logistics, or a related field. Familiarity with ERP systems, inventory tracking software, and certification in supply chain management (such as APICS CPIM) are commonly required. Strong analytical skills, attention to detail, and effective leadership and communication abilities set top performers apart. These skills ensure accurate material flow, cost efficiency, and seamless coordination within the supply chain, which are vital for organizational success.

What are some common challenges faced by material control managers, and how can they be addressed?

Material Control Managers often encounter challenges such as inventory discrepancies, supply chain disruptions, and communication gaps between departments. To address these issues, it’s important to implement robust inventory tracking systems, establish clear procedures for material handling, and foster strong collaboration with purchasing, production, and logistics teams. Regular audits and continuous process improvements can also help maintain accurate inventory levels and ensure timely material flow, which is critical for meeting production schedules and minimizing costs.

What is the difference between Material Control Manager vs Inventory Control Supervisor?

AspectMaterial Control ManagerInventory Control Supervisor
CertificationsSupply Chain, Logistics, or Materials Management certificationsInventory Management certifications, such as APICS CSCP
Work EnvironmentManufacturing, construction, or industrial settingsWarehouses, distribution centers, manufacturing plants
Employer & Industry UsageUsed in industries requiring complex material planning and controlCommon in retail, manufacturing, and logistics sectors

The Material Control Manager oversees the planning, procurement, and management of materials to ensure smooth production flow, often handling complex supply chain processes. The Inventory Control Supervisor focuses on maintaining accurate inventory levels, managing stock counts, and reducing discrepancies. While both roles involve inventory management, the Material Control Manager has a broader scope related to material planning and procurement, whereas the Inventory Control Supervisor concentrates on inventory accuracy and stock control.

What are popular job titles related to Material Control Manager jobs in Irvine, CA?

For Material Control Manager jobs in Irvine, CA, the most frequently searched job titles are:

What job categories do people searching Material Control Manager jobs in Irvine, CA look for?

The top searched job categories for Material Control Manager jobs in Irvine, CA are:

What cities near Irvine, CA are hiring for Material Control Manager jobs?

Cities near Irvine, CA with the most Material Control Manager job openings:

Material Control Manager jobs near you
Infographic showing various Material Control Manager job openings in Irvine, CA as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $76,716 per year, or $36.9 per hour.

Quality Control Manager

iRhythm Holdings, Inc.

Orange, CA • On-site

Full-time

Re-posted 4 days ago

Job description

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
About This Role:
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.
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

What You Will Be Doing
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.

Location:
Orange County
Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location.
Estimated Pay Range
$112,000.00 - $145,000.00
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 taops@irhythmtech.com
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 taops@irhythmtech.com. 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

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