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Traveling Quality Control Manager Jobs in Riverside, CA

VPET USA, LLC

QC Manager

Fontana, CA

Quality Control Manager Salary Status: DOE FLSA: Exempt Employment Type: Full-Time Location ... 20% travel to support other facilities. Education and/or Experience: • Bachelor's Degree ...

VPET USA LLC

QC Manager

Fontana, CA · On-site

Quality Control Manager Salary Status: DOE FLSA: Exempt Employment Type: Full-Time Location ... 20% travel to support other facilities. Education and/or Experience: • Bachelor's Degree ...

ADURA LLC

Quality Control Manager

Corona, CA

$100K - $120K/yr

Quality Control Manager - PCB/ PCB - A Manufacturing Full-Time, Based in Corona, CA, Work hours are 8AM to 4.30PM, Salaried employee. Benefits - 401K, PTO, Sick Leave, Medical/Dental/Vision Insurance ...

Turner Mining Group

Travelling QC Technician

Anaheim, CA

$47K - $52K/yr

... Traveling Quality Control Technician Specialist to support field operations across multiple project sites. This role partners closely with Superintendents and Project Management teams to ensure all ...

Turner Mining Group

Travelling QC Technician

Anaheim, CA · On-site

$47K - $52K/yr

... Traveling Quality Control Technician Specialist to support field operations across multiple project sites. This role partners closely with Superintendents and Project Management teams to ensure all ...

Turner Mining Group

Travelling QC Technician

Anaheim, CA · On-site

$19.75 - $25.25/hr

... Traveling Quality Control Technician Specialist to support field operations across multiple project sites. This role partners closely with Superintendents and Project Management teams to ensure all ...

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 ...

VPET USA LLC

QC Lead (2nd shift)

Fontana, CA · On-site

Quality Control Inspector Lead Location: Fontana, CA, 92337 In the Quality Control Inspector Lead ... Quality Management: Assure that employees operate consistently within the policies and procedures ...

Dycom Industries, Inc.

Manager Quality Control

Upland, CA · On-site

$90K - $115K/yr

We are looking for a Manager of Quality Control Field who is passionate about building "boots on the ground" excellence and mentoring the next generation of industry experts. Join a team that ...

CEMEX

Manager Quality Control Aggregates

Rialto, CA

... performance management, and professional development for Quality Control personnel, including ... Frequent travel between plant, laboratory, and customer locations may be required. Physical ...

Nongshim USA INC

Quality Control

Rancho Cucamonga, CA · On-site

$21.50 - $23/hr

Quality Control Staff Job Summary: The QC Tech is responsible for supporting the Quality Control ... QA management. * Maintain lab cleanliness and chemical inventory. * Dispose of chemical waste in ...

VPET USA LLC

QC Inspector

Fontana, CA · On-site

This role supports company initiatives, provides training and assists the Quality Control Manager. Essential Responsibilities: * Comply with all quality, safety, and work rules and regulations.

Avid Bioservices

Supervisor, Quality Control

Tustin, CA · On-site

$86.40 - $108/hr

Attend and manage weekly contract laboratory meetings and provide status updates to required ... Minimal overnight travel by land and/or air may be required. * Perform other duties as assigned.

Avid Bioservices

Supervisor, Quality Control

Tustin, CA · On-site

$86K - $108K/yr

Attend and manage weekly contract laboratory meetings and provide status updates to required ... Minimal overnight travel by land and/or air may be required. * Perform other duties as assigned.

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All JobsTraveling Quality Control JobsTraveling Quality Control Manager JobsTraveling Quality Control Manager Jobs in Riverside, CA

Traveling Quality Control Manager information

See Riverside, CA salary details

$51.6K

$102.3K

$140.3K

How much do traveling quality control manager jobs pay per year?

As of Aug 27, 2026, the average yearly pay for traveling quality control manager in Riverside, CA is $102,316.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,100.00 and $115,800.00 per year, depending on experience, location, and employer.

What is a traveling quality control manager?

A Traveling Quality Control Manager is a professional responsible for ensuring that products or services meet quality standards across multiple job sites or locations. They travel to different facilities or project sites to inspect processes, perform audits, implement quality control procedures, and train local staff. Their role is crucial in maintaining consistency and compliance with industry regulations, regardless of where the work is performed. This position often requires strong communication skills, attention to detail, and the ability to adapt to different environments. Traveling Quality Control Managers are common in industries such as construction, manufacturing, and food production.

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

To thrive as a Traveling Quality Control Manager, you need a solid background in quality assurance processes, industry regulations, and a relevant degree such as engineering or construction management. Familiarity with quality management systems (QMS), auditing tools, and certifications like ISO 9001 Lead Auditor are typically required. Strong problem-solving, communication, and adaptability are crucial soft skills, especially when working across multiple sites and teams. These skills ensure consistent quality standards, regulatory compliance, and effective coordination in dynamic, multi-location environments.

What are some unique challenges faced by a traveling quality control manager, and how can they be addressed?

A Traveling Quality Control Manager often faces the challenge of adapting to diverse work environments and varying quality standards across different sites. They must quickly build rapport with local teams and ensure consistent implementation of company policies despite regional differences. Effective communication, strong organizational skills, and adaptability are key to overcoming these obstacles. Utilizing standardized checklists and remote collaboration tools can help maintain uniform quality assurance processes across all locations.

What is the difference between Traveling Quality Control Manager vs Quality Assurance Inspector?

AspectTraveling Quality Control ManagerQuality Assurance Inspector
CredentialsTypically requires a degree in engineering or quality management, certifications like ASQ CQEUsually requires a high school diploma or associate degree, certifications like ASQ CQI
Work EnvironmentOversees multiple sites, travels frequently, manages quality processesWorks mainly on-site inspecting products or processes at a specific location
Employer & Industry UsageUsed in manufacturing, construction, and engineering firms with multiple locationsCommon in manufacturing, production lines, and quality departments

The Traveling Quality Control Manager and Quality Assurance Inspector both focus on quality standards, but the manager oversees multiple sites and manages quality programs, often traveling between locations. The inspector performs on-site inspections at a single location, focusing on product or process compliance. Both roles require quality certifications, but the manager's role is broader and more strategic.

What are popular job titles related to Traveling Quality Control Manager jobs in Riverside, CA?

For Traveling Quality Control Manager jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Traveling Quality Control Manager jobs in Riverside, CA look for?

The top searched job categories for Traveling Quality Control Manager jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Traveling Quality Control Manager jobs?

Cities near Riverside, CA with the most Traveling Quality Control Manager job openings:

Traveling Quality Control Manager jobs near you
Infographic showing various Traveling Quality Control Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $102,316 per year, or $49.2 per hour.

Quality Control Manager

Orange, CA • On-site

iRhythm Holdings, Inc.
See more jobs at iRhythm Holdings, Inc.external

Full-time

Re-posted 8 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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