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Entry Level Quality Control Jobs in Riverside, CA

... design control documentation, including threat modeling records, vulnerability assessments ... Security+, ISC2 CC, or similar entry-level cybersecurity certification is a plus. Education:

Engineer I, Quality

Ontario, CA · On-site

$96.76/hr

... stability control products; steering parts; multimedia systems; UVO systems; injection-molded ... Description This is an entry level position where initially the engineer has a low level of ...

Assembly Technician I

Fontana, CA

$17.75 - $22.25/hr

Performs quality control checks of the mobile units prior to dispatch. Completes appropriate shift ... ENTRY LEVEL, non-exempt position. QUALIFICATIONS High School Diploma or equivalent such as G.E.D.

Warehouse Associate

Anaheim, CA · On-site

$16.75 - $20/hr

As this is an entry level role, experience is less important than personal integrity and a strong ... Reshelve equipment that does not require quality Control (QC) * Pull and prep orders with ...

Be Seen First

Perform quality control to ensure product standards * Label products clearly and correctly * Palletize items for efficient storage and transport Preferred Qualifications * Entry-level experience in ...

Assembly Technician I

Fontana, CA · On-site

$17.75 - $22.25/hr

Performs quality control checks of the mobile units prior to dispatch. Completes appropriate shift ... ENTRY LEVEL, non-exempt position. QUALIFICATIONS High School Diploma or equivalent such as G.E.D.

Customer Care Associate

Irvine, CA · On-site

$15.50 - $21.50/hr

Resolve quality control issues as they arise. * Participate in the 10 step AVID-Customer ... Meritage is committed to building energy-efficient and affordable entry-level and first move-up ...

Showing results 21-40

Entry Level Quality Control information

See Riverside, CA salary details

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How much do entry level quality control jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for entry level quality control in Riverside, CA is $21.87, according to ZipRecruiter salary data. Most workers in this role earn between $18.80 and $24.09 per hour, depending on experience, location, and employer.

What is an entry level quality control?

An Entry Level Quality Control job involves inspecting products, materials, or processes to ensure they meet company and industry standards. Responsibilities typically include conducting quality tests, documenting findings, and reporting defects to supervisors. This role helps maintain product consistency, safety, and compliance. Strong attention to detail and basic knowledge of quality assurance principles are key for success in this position.

What are the typical daily tasks of an entry level quality control?

Entry Level Quality Control professionals are usually responsible for inspecting materials or products for defects, running basic tests, documenting results, and reporting any inconsistencies to supervisors. You may also assist in maintaining inspection equipment, preparing sample materials, and supporting compliance with company or industry standards. The role often involves working closely with production teams to identify and resolve quality issues promptly. Regular collaboration and attention to detail are key, as your findings help maintain the overall quality of products and smooth workflow within the facility.

What are the key skills and qualifications needed for an entry level quality control?

To thrive as an Entry Level Quality Control professional, you need strong attention to detail, basic knowledge of quality assurance processes, and a high school diploma or relevant technical training. Familiarity with measurement tools like calipers, micrometers, and computerized inspection systems is often required, and some positions may value certification such as Six Sigma White Belt. Reliability, clear communication, and a willingness to learn are essential soft skills for this role. These abilities ensure accurate inspections, effective teamwork, and consistent delivery of products that meet quality standards.

How to enter a career in entry level quality control?

To start a career in entry-level quality control, candidates typically need a high school diploma or equivalent and should develop skills in attention to detail, inspection techniques, and basic understanding of manufacturing or production processes. Gaining experience through internships or on-the-job training can be beneficial, and some employers may prefer candidates with certifications such as Six Sigma or quality assurance training. Familiarity with tools like calipers, gauges, and quality management software can also improve job prospects.

Is entry level quality control a good entry-level job?

Entry level quality control positions are suitable for individuals seeking to gain industry experience, often requiring attention to detail and basic inspection skills. These roles typically involve working in manufacturing or production environments and may require training on specific tools or standards. They can serve as a stepping stone to more advanced quality assurance or supervisory roles.

What are the most commonly searched types of Quality Control jobs in Riverside, CA?

The most popular types of Quality Control jobs in Riverside, CA are:

What are popular job titles related to Entry Level Quality Control jobs in Riverside, CA?

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

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

The top searched job categories for Entry Level Quality Control jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Entry Level Quality Control jobs?

Cities near Riverside, CA with the most Entry Level Quality Control job openings:

Infographic showing various Entry Level Quality Control job openings in Riverside, CA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $45,499 per year, or $21.9 per hour.

Cybersecurity Quality Engineer

Masimo

Irvine, CA • On-site

$85K - $105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 21 days ago


Job description


Job Summary:
The Cybersecurity Quality Engineer supports the integration of cybersecurity requirements into the product development lifecycle and quality management system for Masimo medical device products. Working under the guidance of senior quality, software, and cybersecurity team members, this role assists in ensuring cybersecurity-related activities are documented, traceable, and executed in accordance with applicable regulatory requirements, quality system procedures, and internal standards. This is an early-career engineering role suited for an individual seeking to develop specialized experience at the intersection of quality systems, design controls, software quality, and medical device cybersecurity.
Duties & Responsibilities:
  • Support execution of cybersecurity quality activities across assigned product development programs, including documentation review, milestone tracking, and quality record maintenance.
  • Assist in the preparation, review, and maintenance of cybersecurity-related design control documentation, including threat modeling records, vulnerability assessments, security risk analyses, cybersecurity protocols, and test reports.
  • Maintain traceability between cybersecurity requirements, software design outputs, mitigation activities, and verification/validation records within the Design History File (DHF).
  • Support authoring, review, and periodic updates of cybersecurity-related quality system procedures, work instructions, templates, and documentation standards.
  • Assist in cybersecurity vulnerability monitoring and post-market surveillance activities, including tracking disclosed vulnerabilities, supporting impact assessments, and documenting remediation activities.
  • Support management of cybersecurity-related nonconformances, CAPAs, deviations, and engineering changes through the quality management system, ensuring accurate documentation and timely follow-up.
  • Participate in cross-functional design reviews, cybersecurity risk reviews, and project meetings, supporting quality representation for cybersecurity-related topics.
  • Collaborate with R&D, Software Engineering, Regulatory Affairs, Product Security, and Quality teams to support consistent application of cybersecurity quality requirements across development activities.
  • Support preparation of cybersecurity documentation required for audits, regulatory submissions, inspections, and internal quality reviews.
  • Assist in evaluation of third-party software components, open-source software dependencies, and Software Bill of Materials (SBOM) documentation to support cybersecurity traceability and risk awareness.
  • Support internal audits, readiness activities, and documentation reviews related to cybersecurity quality and design control compliance.
  • Stay current with evolving regulatory guidance, industry standards, and cybersecurity best practices relevant to medical device development.

Minimum & Preferred Qualifications and Experience:
Minimum Qualifications:
  • Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering, Biomedical Engineering, Software Engineering, or related technical discipline.
  • 0-3 years of experience in quality engineering, software quality, cybersecurity, product security, or related engineering field; relevant internship, co-op, or project-based experience in regulated environments will be considered.
  • Foundational understanding of cybersecurity concepts including vulnerability management, threat modeling, software security, network security, and secure development principles.
  • Familiarity with quality systems, design controls, software lifecycle documentation, or regulated engineering processes.
  • Strong attention to detail and ability to manage documentation accurately.
  • Effective written and verbal communication skills.
  • Ability to manage multiple tasks and priorities in a dynamic, cross-functional environment.

Preferred Qualifications:
  • Exposure to medical device, healthcare technology, embedded systems, or regulated software environments.
  • Familiarity with FDA 21 CFR Part 820, ISO 13485, ISO 14971, FDA cybersecurity guidance, or related regulatory expectations.
  • Awareness of standards such as AAMI TIR57, IEC 62304, IEC 81001-5-1, or NIST cybersecurity frameworks.
  • Exposure to Software Bill of Materials (SBOM), software traceability, or software quality documentation practices.
  • Foundational knowledge of software validation, software quality assurance, or secure SDLC practices.
  • Security+, ISC2 CC, or similar entry-level cybersecurity certification is a plus.

Education:
Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering, Biomedical Engineering, Software Engineering, or related technical discipline, or equivalent combination of education and experience.
Compensation: The anticipated salary range for this position is $85,000 -$105,000. Actual placement within the range is dependent on multiple factors, including but not limited to skills, experience and internal equity. This position also qualifies for up to 10% annual bonus based on Company, department, and individual performance.
  • Masimo offers benefits such as Medical, Dental, Vision, Life/AD&D, Disability Insurance, 401(k), Vacation, Sick, Holiday, Paid Maternity Leave, Flexible Spending Accounts, voluntary Accident, Critical Illness, Hospital, Long-Term Care, Employee Assistance Program, Pet Insurance, on-site Wellness Clinic, Fitness Center, Café. All benefits are subject to eligibility requirements.

Language requirements
  • Ability to read, write, and communicate effectively in English.
  • Ability to interpret technical documents, engineering data, schematics, and written procedures.
  • Ability to clearly document technical findings and effectively communicate across cross-functional teams.
Physical requirements/Work Environment
  • This position primarily works in an office environment and requires frequent sitting, standing, and walking. Daily use of a computer and other digital devices is required. This role may require standing for extended periods when facilitating meetings, supporting laboratory activities, or walking through facilities.
  • Must be able to move throughout office, laboratory, and light manufacturing environments as needed to support design reviews, product inspections, audits, and cross-functional collaboration.
  • Occasional lifting and carrying of materials or equipment up to 25 lbs. may be required.
  • Domestic and international travel up to 20-25% may be required to support supplier visits, audits, customer activities, or program-related meetings.
  • The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods. Reasonable accommodations may be made for those individuals with real or perceived disabilities to perform the essential functions of the job described.

Masimo is proud to be an EEOE/, M/F/D/V, and we are committed to Diversity at the corporate level.

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About Masimo

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Irvine, CA, US

Year founded

1989

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