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Qa Incoming Inspector Jobs in Riverside, CA (NOW HIRING)

CTK USA INC

QC Manager

Corona, CA · On-site

You will directly supervise the QC Laboratory Technicians and the Package Incoming Inspector, and ... Lead OOS/OOT Phase I laboratory investigations and support QA-led Phase II investigations * Perform ...

TST MASTER

QA Inspector

Fontana, CA · On-site

$20.50 - $21.25/hr

Performs inspections during casting at key points to determine quality of product according to Work instruction. * Monitors and ensures proper markings and relocation of quarantined material.

TST MASTER

QA Inspector

Fontana, CA · On-site

$20.50 - $21.25/hr

Performs inspections during casting at key points to determine quality of product according to Work instruction. * Monitors and ensures proper markings and relocation of quarantined material.

Developlus, Inc.

Quality Assurance Lab Technician

Corona, CA · On-site

$20.50 - $25.75/hr

The Quality Assurance/Lab Technician at Developlus Inc. ensures the consistent quality of ... Perform incoming inspections for raw materials, sampling and testing to ensure compliance with ...

F&S Fresh Foods

Quality Assurance Technician

Riverside, CA · On-site

$18 - $22/hr

... incoming materials, in-process production, and finished products at our Riverside, CA facility ... What You'll Own Conduct pre-operation and in-process inspections to verify food safety and quality ...

Epic Personnel Partners, LLC

Be Seen First

Food Quality Assurance Supervisor

Fontana, CA · On-site

$70K/yr

... quality inspection and product release programs for incoming and in-process materials and ... Knowledge of MSDS · Ensure that all quality assurance programs and procedures are being ...

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Qa Incoming Inspector information

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How much do qa incoming inspector jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for qa incoming inspector in Riverside, CA is $23.82, according to ZipRecruiter salary data. Most workers in this role earn between $18.32 and $26.83 per hour, depending on experience, location, and employer.

What is a QA Incoming Inspector?

QA Incoming Inspectors are quality assurance professionals responsible for inspecting and verifying the quality of materials, parts, or products received from suppliers before they are used in manufacturing or production processes. Their main duties include conducting visual and measurement inspections, documenting findings, and ensuring that incoming goods meet established specifications and standards. They help prevent defective or non-conforming materials from entering the production line, which is crucial for maintaining product quality and safety.

What are the key skills and qualifications needed to thrive as a QA Incoming Inspector?

To thrive as a QA Incoming Inspector, you need a solid understanding of quality assurance principles, inspection techniques, and familiarity with industry standards, often supported by a high school diploma or technical certification. Experience with measurement tools, ERP systems, and quality control software is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for accurately identifying and reporting defects. These skills ensure only compliant materials enter production, safeguarding product quality and organizational reputation.

What are some typical challenges faced by a QA Incoming Inspector and how can they be addressed?

QA Incoming Inspectors often encounter challenges such as handling large volumes of incoming materials, ensuring accurate documentation, and identifying non-conforming parts under tight deadlines. To address these, strong organizational skills, attention to detail, and effective communication with suppliers and internal teams are essential. Leveraging digital inspection tools and maintaining clear records can also streamline the process and reduce errors, leading to smoother operations and improved product quality.

What is the difference between Qa Incoming Inspector vs Qa Quality Auditor?

AspectQa Incoming InspectorQa Quality Auditor
CertificationsISO 9001, ASQ certifications often preferredISO 9001, ASQ certifications often preferred
Work EnvironmentInspection of incoming materials at receiving docks or warehousesAuditing quality systems across departments or facilities
Employer & Industry UsageManufacturing, automotive, electronicsManufacturing, pharmaceuticals, food industry
Search & Comparison IntentDifferences in roles, responsibilities, and skillsComparison of quality assurance roles

The Qa Incoming Inspector primarily focuses on inspecting incoming materials to ensure quality before production. In contrast, the Qa Quality Auditor evaluates overall quality systems and processes across the organization. Both roles require similar certifications and are common in manufacturing industries, but their responsibilities differ in scope and focus.

How to become a QA Incoming Inspector?

To become a QA Incoming Inspector, candidates typically need a high school diploma or equivalent, along with experience in quality control or inspection roles. Relevant skills include attention to detail, knowledge of inspection tools and standards, and sometimes certifications like ASQ Certified Quality Inspector (CQI). Familiarity with industry-specific regulations and the ability to operate measurement instruments are also beneficial.

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For Qa Incoming Inspector jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Qa Incoming Inspector jobs in Riverside, CA look for?

The top searched job categories for Qa Incoming Inspector jobs in Riverside, CA are:

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Cities near Riverside, CA with the most Qa Incoming Inspector job openings:

Qa Incoming Inspector jobs near you
Infographic showing various Qa Incoming Inspector job openings in Riverside, CA as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $49,551 per year, or $23.8 per hour.

QC Manager

Corona, CA • On-site

CTK USA INC
1 - 10 employees
Learn more about CTK USA INCexternal

Full-time

Medical, PTO

Posted 4 days ago

Job description

About the Role

CTK OTC Laboratories is seeking an experienced Quality Control Manager to lead our QC laboratory operations for OTC monograph drug and cosmetic products. Reporting to the QD Director, you will oversee physicochemical and microbiological testing, the stability program, environmental monitoring execution, and laboratory data integrity. You will determine technical conformance of tested materials, lead Phase I laboratory investigations of OOS/OOT results, and develop specifications and analytical methods — all in compliance with 21 CFR 210/211 and FDA OOS Guidance.


You will directly supervise the QC Laboratory Technicians and the Package Incoming Inspector, and own the day-to-day performance of the QC laboratory.


What You'll Do

  • Manage physicochemical testing of raw materials, in-process materials, and finished products, and perform first-level review of results
  • Manage microbial limit testing and environmental monitoring (EM) execution
  • Determine technical conformance of raw materials, packaging components, and in-process materials, and report results to QA for disposition
  • Operate the stability testing program, manage stability results, and recommend expiration dating
  • Develop specifications and technical justifications for raw materials, in-process materials, finished products, and purified water for QA approval
  • Execute and technically review analytical method validation protocols and reports
  • Lead OOS/OOT Phase I laboratory investigations and support QA-led Phase II investigations
  • Perform first-level review of electronic data audit trails and oversee laboratory system CSV
  • Manage laboratory instrument calibration, maintenance, and the Daily Verification program
  • Oversee reference standards, reagents, and retain sample management
  • Manage purified water testing and monitoring, and monitor storage/stability chamber conditions
  • Execute tamper-evident packaging inspection (21 CFR 211.132) and testing/quality evaluation of returned and recalled products
  • Manage laboratory data integrity (ALCOA+) compliance and provide trend data for the Annual Product Review


Leadership Responsibilities

  • Directly supervise, train, and evaluate the QC Laboratory Technicians and the Package Incoming Inspector
  • Develop and manage QC test method, instrument, and laboratory job-specific training programs (new-hire and periodic refresher)
  • Set day-to-day priorities and workload across the QC laboratory to meet testing and release timelines
  • Build a strong laboratory culture of accurate, contemporaneous documentation and prompt escalation of atypical results


Education & Experience

  • Bachelor's degree in Chemistry, Pharmacy, Pharmaceutical Sciences, Microbiology, Biology, Chemical Engineering preferred but not required
  • Substantial hands-on QC laboratory experience in a cGMP-regulated environment (OTC drug, pharmaceutical, cosmetic, or dietary supplement), including supervisory or managerial experience
  • Demonstrated experience with analytical instrumentation (HPLC/UPLC, GC, UV-Vis, FTIR, Karl Fischer, viscometer) and wet chemistry methods
  • Demonstrated experience with method validation/verification, stability program operation, and microbial limit testing
  • Experience leading Phase I laboratory OOS investigations and preparing investigation reports
  • Experience with laboratory data integrity remediation and audit trail review preferred


Knowledge, Skills & Abilities

  • Thorough working knowledge of 21 CFR Parts 210, 211, and 11, USP general chapters, and FDA OOS Guidance
  • Ability to critically evaluate analytical data and distinguish laboratory error from manufacturing-related causes
  • Ability to author and review specifications, test methods, validation protocols, and investigation reports in English
  • Competent with Microsoft Word, Excel, Outlook, PDF tools, and electronic document/record and inventory systems
  • Proficiency with chromatographic data systems and laboratory electronic records, including audit trail review
  • Effective supervisory and training skills for laboratory personnel
  • Bilingual English/Korean or English/Spanish is a plus


Regulatory Scope

This position determines technical conformance for materials and products tested by the QC laboratory, with final disposition authority resting with QA. The role supports compliance with laboratory controls (21 CFR 211.160–211.167), stability testing (211.166), tamper-evident packaging (211.132), electronic records (Part 11), and data supporting the Annual Product Review (211.180–211.198).


Benefits

  • Health Insurance — premium 100% covered by employer for the employee
  • Paid Time Off (PTO)
  • Paid holidays
  • Annual floating holiday