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Equipment Control Manager Jobs in California (NOW HIRING)

Quality Control Manager

Los Angeles, CA · On-site

$113K - $125K/yr

The QC Manager will coordinate with equipment manufacturers and vendors during project startup to understand quality standards, inspection requirements, and testing procedures. Essential ...

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Capital Brand Group, LLC (CBG) is hiring a Quality Control Manager to own the quality of all work ... equipment: HVAC, electrical, plumbing, fire protection, generators, elevators, water systems ...

Quality Control Manager

Barstow, CA · On-site

$7.0K - $90K/yr

Administer quality control management program * Responsible for overall quality assurance program ... Collect data for the DMLSS system including work orders and equipment history Education, Experience ...

Quality Control Manager

Barstow, CA · On-site

$7.0K - $90K/yr

Administer quality control management program * Responsible for overall quality assurance program ... Collect data for the DMLSS system including work orders and equipment history Education, Experience ...

Quality Control Manager

Santee, CA · On-site

$35 - $45/hr

Quality Control Manager (Aerospace CNC Manufacturing) Location: Santee, CA Job Type: Full-Time ... Oversee inspection activities using precision measuring equipment, including: * Micrometers

Quality Control Manager

San Carlos, CA · On-site

$95K - $195K/yr

Overview Quality Control Manager (Inspection Team) Joby Aviation is seeking a Quality Control ... Strong practical expertise with manufacturing inspection tools, measurement equipment, precision ...

Quality Control Manager

San Carlos, CA · On-site

$95K - $195K/yr

Overview Quality Control Manager (Inspection Team)Joby Aviation is seeking a Quality Control ... Strong practical expertise with manufacturing inspection tools, measurement equipment, precision ...

Quality Control Manager

San Carlos, CA · On-site

$95K - $195K/yr

Quality Control Manager (Inspection Team) Joby Aviation is seeking a Quality Control Manager to ... Strong practical expertise with manufacturing inspection tools, measurement equipment, precision ...

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Quality Control Manager

Rohnert Park, CA · On-site

$75K - $100K/yr

Quality Control (QC) Manager in a metal manufacturing company is responsible for ensuring that raw ... Maintain calibration of measuring and testing equipment * Lead internal and external audits

This role routinely uses standard office equipment such as computers, phones, photocopiers, and ... This Quality Control Manager, QCM, role is relocating from project site to project site. * Typical ...

Lead and manage all Quality Control operations, including Receiving Inspection, In-Process ... Manage the calibration program for inspection and test equipment, ensuring measurement devices are ...

New

This role routinely uses standard office equipment such as computers, phones, photocopiers, and ... This Quality Control Manager, QCM, role is relocating from project site to project site. * Typical ...

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Equipment Control Manager information

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

Equipment Control Managers often face challenges in maintaining accurate inventory records, coordinating equipment availability, and minimizing downtime due to equipment shortages or malfunctions. Effective communication with operations, maintenance, and logistics teams is essential to quickly resolve issues and ensure equipment is allocated efficiently. Utilizing modern asset management software and establishing clear processes can greatly improve tracking accuracy and help prevent losses, while regular training for staff helps uphold compliance and safety standards.

What are the key skills and qualifications needed to thrive as an equipment control manager, and why are they important?

To thrive as an Equipment Control Manager, you need a solid understanding of logistics management, inventory control, and supply chain processes, typically supported by a relevant bachelor’s degree or industry experience. Familiarity with asset tracking software, enterprise resource planning (ERP) systems, and possibly certifications like APICS or Six Sigma is often required. Strong organizational skills, attention to detail, and effective leadership and communication abilities are crucial soft skills in this role. These competencies ensure efficient equipment utilization, minimize losses, and support seamless operations in dynamic environments.

What is the difference between Equipment Control Manager vs Equipment Coordinator?

AspectEquipment Control ManagerEquipment Coordinator
ResponsibilitiesOversees equipment inventory, maintenance scheduling, and asset management at a managerial level.Assists with equipment tracking, setup, and basic maintenance tasks under supervision.
CredentialsTypically requires relevant certifications or experience in equipment management or logistics.Often requires basic technical knowledge; certifications are less common.
Work EnvironmentWorks in warehouses, production facilities, or logistics centers, managing teams and processes.Works in similar environments, focusing on operational support and coordination.

The Equipment Control Manager and Equipment Coordinator roles share similarities in work environment and industry usage but differ mainly in scope and responsibility. The manager oversees the entire equipment inventory and processes, while the coordinator supports daily operations. Both roles require relevant technical knowledge, but the manager typically holds more advanced credentials and leadership duties.

What does an equipment control manager do?

An Equipment Control Manager is responsible for overseeing the tracking, allocation, and maintenance of equipment within an organization, often in industries like shipping, construction, or logistics. They ensure that all equipment is efficiently utilized, maintained in good working condition, and correctly inventoried to meet operational needs. Their role includes coordinating with different departments, managing equipment records, and implementing systems to prevent loss or misuse. Effective Equipment Control Managers help reduce costs and improve productivity by optimizing equipment usage.
What are the most commonly searched types of Equipment Control jobs in California? The most popular types of Equipment Control jobs in California are:
What cities in California are hiring for Equipment Control Manager jobs? Cities in California with the most Equipment Control Manager job openings:

Quality Control Manager

iRhythm Holdings, Inc.

Orange, CA • On-site

Full-time

Re-posted 22 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