ZipRecruiter

Log In

1

Cement Quality Control Manager 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

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 ...

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 ...

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.

CEMEX

Manager Quality Control Aggregates

Rialto, CA · On-site

Provide leadership, direction, coaching, mentoring, performance management, and professional development for Quality Control personnel, including technicians and supervisors, while fostering a ...

CEMEX

Manager Quality Control Aggregates

Rialto, CA · On-site

$85K - $108K/yr

Formulates and maintains quality control objectives * Coordinates objectives with production procedures in cooperation with other managers to maximize product reliability and minimize costs * Directs ...

Avid Bioservices

Supervisor, Quality Control

Tustin, CA · On-site

$86.40 - $108/hr

Your Role: The Quality Control Supervisor provides leadership and oversees the day-to-day ... Attend and manage weekly contract laboratory meetings and provide status updates to required ...

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

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 ...

next page

Showing results 1-20

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

Cement Quality Control Manager information

See Riverside, CA salary details

$31.8K

$84.8K

$135.1K

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

As of Aug 27, 2026, the average yearly pay for cement quality control manager 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.

What does a cement quality control manager do?

A Cement Quality Control Manager is responsible for overseeing the quality of cement production to ensure it meets industry standards and specific project requirements. They supervise laboratory testing, monitor production processes, and analyze test results to maintain consistent product quality. Additionally, they work closely with production teams to identify and resolve any issues related to raw materials or finished products. Their goal is to ensure the cement produced is safe, durable, and compliant with all applicable regulations.

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

To thrive as a Cement Quality Control Manager, you need a solid background in chemistry or materials science, experience in cement manufacturing, and a relevant degree such as chemical engineering. Proficiency with laboratory testing equipment, quality assurance systems (like ISO standards), and data analysis software is essential. Strong attention to detail, leadership abilities, and effective communication distinguish top performers in this role. These skills ensure consistent product quality, regulatory compliance, and efficient operations within cement production facilities.

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

Cement Quality Control Managers often face challenges such as maintaining consistent product quality, ensuring compliance with stringent industry regulations, and troubleshooting issues in the production process. These challenges can be addressed by implementing robust quality management systems, staying updated on regulatory changes, and fostering strong communication between laboratory staff, production teams, and management. Additionally, investing in ongoing staff training and modern analytical equipment helps to quickly identify and resolve quality deviations, ensuring the final product meets all required standards.

What is the difference between Cement Quality Control Manager vs Cement Laboratory Technician?

AspectCement Quality Control ManagerCement Laboratory Technician
CredentialsDegree in Civil Engineering, Quality Assurance certificationsDiploma or degree in Chemistry or Materials Testing
Work EnvironmentSupervisory role overseeing quality processes in cement plantsLaboratory setting conducting tests on cement samples
Industry UsageUsed by cement manufacturing companies for quality managementEmployed in labs for testing and analysis of cement properties

The Cement Quality Control Manager focuses on overseeing quality assurance processes and managing teams, while the Cement Laboratory Technician performs testing and analysis in labs. Both roles require related certifications and are integral to cement production quality, but differ in responsibilities and work settings.

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

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

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

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

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

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

Cement Quality Control Manager jobs near you
Infographic showing various Cement Quality Control Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 86% Full Time, and 14% Part Time. Highlights an 100% In-person 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 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

Apply