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Software Quality Jobs in Ohio (NOW HIRING)

The Senior Software QA Engineer is r esponsible for ensuring quality, stability, and data integrity during software and database upgrades of legacy systems. This role focuses on validation, risk ...

The Senior Software QA Engineer is r esponsible for ensuring quality, stability, and data integrity during software and database upgrades of legacy systems. This role focuses on validation, risk ...

The role involves strong experience in software quality assurance and knowledge of QA methodologies, tools, and processes, with a focus on web application testing using Selenium and Cucumber.

The Senior Software QA Engineer is r esponsible for ensuring quality, stability, and data integrity during software and database upgrades of legacy systems. This role focuses on validation, risk ...

The Senior Software QA Engineer is r esponsible for ensuring quality, stability, and data integrity during software and database upgrades of legacy systems. This role focuses on validation, risk ...

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Software Quality information

See Ohio salary details

$11.4K

$112.8K

$158.3K

How much do software quality jobs pay per year?

As of Sep 13, 2026, the average yearly pay for software quality in Ohio is $112,794.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,600.00 and $132,600.00 per year, depending on experience, location, and employer.

What is software quality?

Software quality refers to how well a software product meets the requirements, expectations, and needs of its users. It measures attributes such as reliability, functionality, usability, efficiency, maintainability, and portability. High software quality means the software is free from defects, operates smoothly, and provides a good user experience. Ensuring software quality typically involves processes like testing, reviews, and continuous improvement throughout the software development lifecycle.

What are the key skills and qualifications needed to thrive in software quality?

To thrive in Software Quality, you need a strong understanding of software development life cycles, testing methodologies, and a relevant degree in computer science or a related field. Familiarity with tools like Selenium, JIRA, and test automation frameworks as well as certifications such as ISTQB are highly valued. Attention to detail, analytical thinking, and effective communication set exceptional professionals apart in this field. These skills ensure that software products meet quality standards, reduce defects, and provide reliable user experiences.

How does a software quality professional typically collaborate with developers and other teams during the software development lifecycle?

Software Quality professionals work closely with developers, product managers, and other stakeholders throughout the software development lifecycle. They participate in requirements reviews, design meetings, and sprint planning sessions to ensure quality is considered from the outset. Regular communication with developers helps clarify requirements and quickly address issues found during testing. Additionally, they often coordinate with DevOps and support teams to facilitate smooth deployments and monitor software performance post-release, fostering a collaborative environment focused on continuous improvement.

What is the difference between Software Quality vs Software Tester?

AspectSoftware QualitySoftware Tester
Primary FocusEnsuring overall software quality, process improvement, and defect preventionIdentifying bugs and issues through testing
ResponsibilitiesQuality assurance, process audits, quality metrics analysisExecuting test cases, reporting defects
CredentialsKnowledge of QA methodologies, certifications like ISTQBTesting skills, certifications like ISTQB
Work EnvironmentCollaborates with development, product management, and QA teamsPrimarily involved in testing activities, often in dedicated testing teams

Software Quality professionals focus on the overall quality management and process improvements, while Software Testers concentrate on executing tests to find defects. Both roles are essential in delivering high-quality software, but their scope and responsibilities differ significantly.

Is software quality a good career?

Software quality roles, such as software quality assurance or testing, are in demand as companies prioritize reliable and bug-free products. These jobs often require knowledge of testing tools, scripting, and quality standards, offering stable career growth and opportunities in various industries.

What is the role of software quality?

The role of software quality is to ensure that software products meet specified requirements, are reliable, and function correctly. Software quality professionals develop and implement testing processes, use tools like automated testing frameworks, and adhere to standards such as ISO or CMMI to identify and fix defects, improving overall product performance and user satisfaction.

What are the most commonly searched types of Software Quality jobs in Ohio?

The most popular types of Software Quality jobs in Ohio are:

Infographic showing various Software Quality job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 16% Part Time, 6% Contract, and 1% Nights. Highlights an 81% Physical, 1% Hybrid, and 18% Remote job distribution, with an average salary of $112,794 per year, or $54.2 per hour.

Software Quality Engineer

Cincinnati, OH • On-site

Ruri Software Technologies LLC
Software Development • 11 - 50 employees

Full-time

Re-posted 3 days ago


Job description

Job Title :Quality Engineer
Location: Onsite. Cincinnati, OH
Job Description :
Quality Engineer with 5+ years of experience in the medical device industry, specializing in quality, validation, and manufacturing engineering for surgical products and implants. Experienced in process validation (IQ/OQ/PQ), PFMEA/DFMEA, Gage R&R, SPC, DOE, risk assessments, and supplier qualification within GMP, ISO, and FDA-regulated environments. Proficient in GD&T interpretation, dimensional data analysis, root cause investigation, and new product commercialization. Strong analytical, problem-solving, and cross-functional collaboration skills with a proven ability to drive quality, compliance, and continuous improvement initiatives.
Roles & Responsibilities:
• Experience in a GMP and/or ISO regulated medical industry is required.
• Ability to analyze and present data that facilitates & drives decision making is required.
• The ability to perform "hands on" troubleshooting and problem solving is required Experience working in an FDA regulated environment is preferred.
• Experience working in operations supporting a production environment is preferred Advanced technical training and experience using Statistics, Lean and Six Sigma Methodologies (i.e. Measurement System Analysis, SPC, DOEs, Reliability, etc.) is preferred
• Technical understanding of manufacturing equipment and processes is preferred Process Validation expertise is preferred.
• Ability to read and interpret CMM and dimensional inspection reports.
• Experience with dimensional data analysis utilizing software (Excel or Minitab)
• Experience in Medical Standards and Quality process preferred.
• New product launch experience from through full validation and commercial launch
• Experience with PFMEA/DFMEA's, Gage R&R's, TMV's, Risk Assessments and Control Plan
• Ensures that corrective measures meet acceptable reliability standards, and that documentation is compliant with requirements.
• Performance Component Qualification (Process Characterization, Process Capability Analysis, Test Method Validation, IQ, OQ, PQ, FAI) of new supplier manufactured components.
• Strong communication skills and ability to work well within a multidisciplinary team.
• Proficient with GD&T and interpreting technical drawings.
• Green or Black Belt Six Sigma certification preferred.
Top Skills:
• Process Validation & Quality Engineering (IQ/OQ/PQ, TMV, PFMEA, Gage R&R)
• Statistical Analysis & Six Sigma (SPC, DOE, MSA, Minitab)
• Medical Device Quality Systems (GMP, ISO 13485, FDA Compliance)
Additional Information:
• Bachelor in Mechanical Engineering or equivalent and have min. 5 years' experience working as a Quality, Validation and or Manufacturing Engineering role in a Medical Product industry required.
• Required medical domain experience. Surgical Product and Implants experience preferred.
Years of Experience: 10.00 Years of Experience
Regards
Surya
Surya@rurisoft.com