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Quality Control Manager Usace Jobs in Riverside, CA

ADURA LLC

Quality Control Manager

Corona, CA · On-site

$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 ...

Vpet USA LLC

QC Manager

Fontana, CA · On-site

Quality Control Manager The Quality Manager is responsible for maintaining and improving the company-wide quality system that focuses on customer satisfaction, defect prevention, improved defect ...

VPET USA, LLC

QC Manager

Fontana, CA

Quality Control Manager Salary Status: DOE FLSA: Exempt Employment Type: Full-Time Location: Fontana, CA Reports to: TBD Job Overview: The Quality Manager is responsible for maintaining and improving ...

VPET USA LLC

QC Manager

Fontana, CA · On-site

Quality Control Manager Salary Status: DOE FLSA: Exempt Employment Type: Full-Time Location: Fontana, CA Reports to: TBD Job Overview: The Quality Manager is responsible for maintaining and improving ...

Thompson Pipe

Senior Quality Control Manager

Fontana, CA · On-site

$57.69/hr

Senior Quality Control Manager *Who We are Thompson Pipe Group is a privately held family business of engineers, contractors, and manufacturers based in Rialto, California. From the humble beginnings ...

Klatch Coffee

Lab QC Manager

Rancho Cucamonga, CA · On-site

$20 - $30/hr

Description Primary Responsibilities Lab Management & Quality Control * Oversee green coffee sample processes, including obtaining, receiving samples, sample roasting, cupping, and scoring using ...

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 ...

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.

MAG INSTRUMENT, INC.

Quality Control Supervisor

Ontario, CA · On-site

$35 - $40/hr

Quality Control Supervisor Selected individual will be responsible for supervision and training of ... This person will be the primary contact with upper management, Engineering, Machining, Assembly ...

Urgent

Bal Seal Engineering

QC Supervisor

Lake Forest, CA · On-site

$85K - $105K/yr

The Quality Assurance Supervisor manages the hourly Quality personnel and is their main point of ... Coordinate with Production Control to assist in meeting Production goals and to ensure inspection ...

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All JobsQuality Control Usace JobsQuality Control Manager Usace JobsQuality Control Manager Usace Jobs in Riverside, CA

Quality Control Manager Usace information

See Riverside, CA salary details

$31.8K

$84.8K

$135.1K

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

As of Aug 12, 2026, the average yearly pay for quality control manager usace in Riverside, CA is $84,842.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,100.00 and $104,300.00 per year, depending on experience, location, and employer.

How does a quality control manager at USACE typically collaborate with project teams to ensure compliance with regulations and standards?

A Quality Control Manager working with the US Army Corps of Engineers (USACE) regularly coordinates with project managers, subcontractors, and field staff to review project specifications and ensure all work meets federal, state, and USACE quality requirements. This involves conducting site inspections, reviewing documentation, leading preparatory meetings, and facilitating communication to address quality issues promptly. Collaboration is crucial in this role, as the manager must ensure all team members understand quality expectations and corrective actions are implemented efficiently. This proactive teamwork helps prevent costly rework and keeps the project on schedule.

What does a quality control manager do for USACE projects?

A Quality Control Manager for USACE (U.S. Army Corps of Engineers) projects is responsible for ensuring that all construction work meets the contract specifications, standards, and regulatory requirements set by USACE. This role includes developing and implementing quality control plans, conducting inspections, managing documentation, and coordinating with contractors and engineers to address deficiencies. The QC Manager plays a critical part in preventing construction errors and ensuring project compliance from start to finish.

What are the key skills and qualifications needed to thrive as a quality control manager with the US Army Corps of Engineers (USACE), and why are they important?

A Quality Control Manager with USACE typically requires expertise in construction management, quality assurance principles, and familiarity with government contract specifications, often supported by a relevant degree and prior experience on federal projects. Proficiency with quality management systems, inspection software, and knowledge of USACE-specific protocols such as RMS (Resident Management System) and EM 385-1-1 safety standards is essential. Strong attention to detail, leadership, and effective communication skills help manage teams and ensure compliance with rigorous standards. These capabilities are vital to consistently deliver projects that meet federal requirements, ensure safety, and maintain client satisfaction.

What is the difference between Quality Control Manager Usace vs Quality Control Inspector?

AspectQuality Control Manager UsaceQuality Control Inspector
CertificationsTypically requires certifications like OSHA, NAVFAC, or equivalentOften requires OSHA 10/30, and specific industry certifications
Work EnvironmentOversees large-scale government projects, construction sites, and military facilitiesInspects ongoing work, ensures compliance on-site, and reports findings
ResponsibilitiesDevelops QC plans, manages teams, ensures project compliancePerforms inspections, documents issues, and verifies work quality

The main difference is that the Quality Control Manager Usace holds a leadership role overseeing entire projects and teams, while the Quality Control Inspector focuses on on-site inspections and reporting. Both roles require relevant certifications and are integral to construction quality assurance within government projects.

What are popular job titles related to Quality Control Manager Usace jobs in Riverside, CA? For Quality Control Manager Usace jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Quality Control Manager Usace jobs in Riverside, CA look for? The top searched job categories for Quality Control Manager Usace jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Quality Control Manager Usace jobs? Cities near Riverside, CA with the most Quality Control Manager Usace job openings:
Quality Control Manager Usace jobs near you
Infographic showing various Quality Control Manager Usace job openings in Riverside, CA as of August 2026, with employment types broken down into 95% Full Time, and 5% Nights. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $84,842 per year, or $40.8 per hour.

Quality Control Manager

iRhythm Holdings, Inc.

Orange, CA • On-site

Full-time

Re-posted 23 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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