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Manual Qa Engineer Remote Jobs in Riverside, CA (NOW HIRING)

Qcells

QA Audits & Controls Manager

Irvine, CA · On-site +1

$90K - $120K/yr

Remote work may be considered for exceptional cases. RESPONSIBILITIES: * Conduct post-approval quality assurance (QA) audits of milestone reviews to ensure accuracy, consistency, and compliance with ...

ICF

Construction QA/QC Lead - Disaster Recovery

Irvine, CA · On-site +1

$89K - $119K/yr

Bachelor's degree in Construction Management, Engineering, Architecture, or a related field (or 3 ... Remote position with possible travel to client sites and field offices throughout La County, CA ...

ICF

Construction QA/QC Lead - Disaster Recovery

Riverside, CA · On-site +1

$87K - $115K/yr

Bachelor's degree in Construction Management, Engineering, Architecture, or a related field (or 3 ... Remote position with possible travel to client sites and field offices throughout La County, CA ...

Interlink Technology, Inc.

Be Seen First

Level 1 Help Desk Engineer - Remote

Murrieta, CA · Remote

$20 - $23/hr

We are looking for a Level 1 Help Desk Engineer to provide remote technical support to our clients ... You'll join a small, growing MSP that values quality, accountability, efficiency, and continuous ...

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Manual Qa Engineer Remote information

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$82

How much do manual qa engineer remote jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for manual qa engineer remote in Riverside, CA is $50.64, according to ZipRecruiter salary data. Most workers in this role earn between $39.86 and $57.93 per hour, depending on experience, location, and employer.

What is a manual QA engineer?

Manual QA Engineers are professionals responsible for testing software applications manually to identify bugs, usability issues, and ensure quality before release. Unlike automated QA engineers, they do not rely on scripts or automation tools but instead execute test cases by hand, following predefined procedures or exploring the application as an end user would. Manual QA Engineers play a crucial role in detecting issues early, providing feedback to developers, and helping maintain high product standards. In remote positions, they perform these tasks from a remote location, collaborating with teams via online tools and platforms.

What are the key skills and qualifications needed to thrive as a manual QA engineer remote?

To thrive as a Manual QA Engineer (Remote), you need a solid understanding of software development lifecycles, test case design, bug reporting, and quality assurance principles, typically supported by a degree in computer science or related field. Familiarity with test management tools like Jira, TestRail, or Zephyr, and experience in using defect tracking systems are usually required. Strong attention to detail, analytical thinking, effective communication, and self-motivation are crucial soft skills for success in a remote environment. These abilities ensure that software products are thoroughly tested, defects are accurately reported, and teams collaborate efficiently to maintain high product quality.

What are some common challenges faced by remote manual QA engineers, and how can they be effectively managed?

Remote Manual QA Engineers often face challenges such as coordinating with distributed development teams, ensuring clear communication regarding test requirements, and managing access to testing environments or devices. To overcome these, it's important to leverage collaboration tools like Slack or Jira, maintain detailed documentation, and proactively schedule regular check-ins with team members. Building strong communication habits and staying organized can help ensure thorough test coverage and timely bug reporting, even when working remotely.

What is the difference between Manual Qa Engineer Remote vs Manual Tester Remote?

AspectManual Qa Engineer RemoteManual Tester Remote
CredentialsTypically requires a QA or related certification, experience in testing methodologiesOften requires similar certifications or experience in manual testing
Work EnvironmentRemote, collaborating with development teams, using testing toolsRemote, focusing on executing test cases and reporting bugs
Industry UsageCommon in software development, tech companies, and IT servicesWidely used in software, app development, and tech industries
Search & Comparison IntentPeople comparing roles with similar manual testing responsibilitiesIndividuals seeking manual testing roles similar to QA engineers

The main difference between a Manual Qa Engineer Remote and a Manual Tester Remote lies in scope and responsibilities. QA Engineers often have broader roles, including test planning and process improvement, while Manual Testers focus primarily on executing test cases and bug reporting. Both roles are essential in software quality assurance and are frequently sought in remote tech positions.

What are the most commonly searched types of Manual Qa Engineer jobs in Riverside, CA?

The most popular types of Manual Qa Engineer jobs in Riverside, CA are:

What are popular job titles related to Manual Qa Engineer Remote jobs in Riverside, CA?

For Manual Qa Engineer Remote jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Manual Qa Engineer Remote jobs in Riverside, CA look for?

The top searched job categories for Manual Qa Engineer Remote jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Manual Qa Engineer Remote jobs?

Cities near Riverside, CA with the most Manual Qa Engineer Remote job openings:

Manual Qa Engineer Remote jobs near you
Infographic showing various Manual Qa Engineer Remote job openings in Riverside, CA as of August 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 100% Remote job distribution, with an average salary of $105,338 per year, or $50.6 per hour.

Sr. Quality Assurance Engineer (ISO 13485)

Prismatik

Irvine, CA • On-site, Remote

$99K - $120K/yr

Full-time

Posted 18 days ago

Job description

We're looking for a Sr. QA Engineer to help build quality into every stage of our medical device development and manufacturing. You'll have broad ownership across quality engineering, risk management, CAPA, validation, and our Quality Management System. Working closely with cross-functional teams, you'll solve complex quality challenges, support new products and processes, and help ensure what we build meets the highest standards for safety, performance, and compliance.

Essential Functions:
  • Ensure compliance with applicable regulatory standards, including FDA 21 CFR Part 820, ISO 13485, MDSAP, and EU MDR.
  • Lead and support CAPA investigations, non-conformance management, and root cause analysis using tools such as 8D, Fishbone, and 5 Whys.
  • Own and continuously improve elements of the Quality Management System (QMS), including document control, internal audits, supplier quality, and change control.
  • Collaborate cross-functionally with R&D, Manufacturing, and Regulatory Affairs to support design control, risk management (ISO 14971), and product development lifecycle activities.
  • Lead internal and supplier audits, and support external audits and inspections (e.g., FDA, Notified Bodies).
  • Participate in validation activities (IQ/OQ/PQ) for processes, equipment, and software used in manufacturing and quality operations.
  • Develop, monitor, and analyze quality metrics to identify trends, drive continuous improvement, and ensure effectiveness of corrective actions.
  • Provide quality engineering support to Quality Control, including guidance on inspection methods, metrology, and measurement system capability.
  • Conduct and document investigations of NCRs, complaints, and deviations, providing effective and sustainable corrective and preventive actions based on engineering analysis.
  • Lead and mentor junior engineers, fostering technical growth and reinforcing a culture of quality and compliance.
  • Integrate ISO 14971 risk management and IEC 62366 usability engineering activities within Glidewell/Prismatik processes.
  • Ensure organizational compliance with the QMS through ongoing training, education, and internal communication.
  • Collaborate with Manufacturing and Engineering to coordinate pilot production, process validations, and risk analyses for new products and processes.
  • Ensure calibration and preventive maintenance systems meet compliance and operational requirements.
  • Identify and implement process optimizations using Lean and Six Sigma methodologies to improve manufacturability, reduce risk, and enhance efficiency.
  • Identify opportunities for design or re-design of equipment, tools, and fixtures to improve manufacturing processes and product quality.
  • Perform other related duties and special projects as assigned by management.
Minimum Qualifications:
  • Bachelor's degree in Engineering, Science, or a related technical field.
  • Minimum of 5 years of experience in Quality Assurance or Quality Engineering within the medical device industry, or equivalent education and experience demonstrating comparable skills and knowledge.
  • Strong working knowledge of FDA regulations, ISO 13485, and other applicable international quality standards.
  • Hands-on experience with risk management (ISO 14971), design controls, and validation methodologies.
  • Proven analytical, problem-solving, and communication skills.
  • Proficiency in quality and statistical analysis tools such as Minitab or equivalent software.
  • Demonstrated project management experience.
  • Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or Six Sigma certification, preferred.
  • Experience with combination products or Class I/II medical devices, preferred.
  • Familiarity with EU MDR and UDI regulatory requirements, preferred.
Pay range: $99,000 - $120,000/yr.
Exact compensation may vary based on skills and experience.
This role is fully onsite at our Irvine, CA campus. Remote or hybrid arrangements are not available.
Employment Type: full-time

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