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Manual Qa Engineer Jobs in Rochester, NY (NOW HIRING)

Ralliant

Quality Assurance Engineer

Fairport, NY · On-site

Customer Quality Engineer / Professional The Customer Quality Engineer (CQE) is responsible for ensuring that Iris Power products meet or exceed customer expectations throughout the product lifecycle.

BCC Software

QA Engineering Manager

Pittsford, NY

The QA Engineering Manager is responsible for leading and advancing quality assurance engineering practices across a diverse portfolio of desktop and SaaS products. This position is accountable for ...

BCC Software

QA Engineering Manager

Pittsford, NY · On-site

The QA Engineering Manager is responsible for leading and advancing quality assurance engineering practices across a diverse portfolio of desktop and SaaS products. This position is accountable for ...

BCC Software

QA Engineering Manager

Pittsford, NY · On-site

The QA Engineering Manager is responsible for leading and advancing quality assurance engineering practices across a diverse portfolio of desktop and SaaS products. This position is accountable for ...

Keenfinity

Associate QA Test Engineer

Fairport, NY · On-site

$65K - $72K/yr

We are seeking a motivated and detail-oriented Associate QA Test Engineer I to join our Product ... This role is responsible for performing manual testing of intrusion detection and security system ...

groteindustries

Quality Assurance Manager

Avon, NY

Bachelor's degree in Quality Engineering, Engineering, Business, or other related field of study. Minimum of 5 years of experience in Quality Assurance, minimum of 2 to 3 years of project management ...

Grote Industries

Quality Assurance Manager

Avon, NY · On-site

$105K - $120K/yr

Bachelor's degree in Quality Engineering, Engineering, Business, or other related field of study. Minimum of 5 years of experience in Quality Assurance, minimum of 2 to 3 years of project management ...

Collabera

Quality Assurance

Rochester, NY

Performs work flow analysis and recommends quality improvements. * Escalates software process issues to appropriate levels of management. * Works independently within defined parameters, taking ...

Vista Robotics

Software QA Intern

Geneseo, NY · On-site

$18.50 - $24.25/hr

We are looking for a Software QA Intern to join Vista Robotics, a leading company in the field of computer software and engineering. As a Software AQ Intern, you will play a crucial role in ensuring ...

Vista Robotics

Software QA Intern

Rochester, NY · On-site

$19 - $25/hr

We are looking for a Software QA Intern to join Vista Robotics, a leading company in the field of computer software and engineering. As a Software AQ Intern, you will play a crucial role in ensuring ...

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All JobsManual Qa Engineer JobsManual Qa Engineer Jobs in Rochester, NY

Manual Qa Engineer information

See Rochester, NY salary details

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How much do manual qa engineer jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for manual qa engineer in Rochester, NY is $47.90, according to ZipRecruiter salary data. Most workers in this role earn between $37.69 and $54.81 per hour, depending on experience, location, and employer.

What is a Manual QA Engineer job?

A Manual QA Engineer is responsible for testing software applications to identify bugs, ensure functionality, and improve overall quality. They execute test cases manually without automation tools, validating that the software meets requirements. Their role includes creating test plans, documenting defects, and collaborating with developers to resolve issues. Strong analytical skills, attention to detail, and knowledge of testing methodologies are essential for success in this role.

Is manual QA in demand?

Manual QA Engineers are still in demand as they play a crucial role in testing software for usability and bugs, especially in environments where automated testing is not fully implemented. Many companies seek professionals with strong attention to detail, knowledge of testing tools, and understanding of software development cycles, making manual QA a valuable skill in the tech industry.

What are typical day-to-day responsibilities for a Manual QA Engineer?

As a Manual QA Engineer, your daily tasks typically include reviewing requirements, designing and executing manual test cases, and logging defects found during testing. You'll frequently collaborate with developers and product managers to clarify issues, verify bug fixes, and ensure thorough coverage of new features or changes. Manual QA Engineers also help document testing results, participate in daily stand-ups, and support regression testing before software releases. This variety keeps the role engaging and gives you valuable insight into the overall software development process.

Is QA Engineer still in demand?

QA Engineer roles remain in demand as companies prioritize software quality assurance, especially with the growth of agile development and automation tools like Selenium and JIRA. Skilled QA professionals with knowledge of testing methodologies, scripting, and tools are sought after across various industries to ensure product reliability and user satisfaction.

How much do manual QA testers make a month?

Manual QA testers typically earn between $2,500 and $5,000 per month, depending on experience, location, and industry. Entry-level testers may earn less, while those with specialized skills or certifications can command higher salaries. Salaries can also vary based on whether the role is full-time, part-time, or contract-based.

What are the key skills and qualifications needed to thrive in the Manual Qa Engineer position, and why are they important?

To thrive as a Manual QA Engineer, you need a solid understanding of software testing methodologies, attention to detail, and the ability to create and execute test cases based on technical requirements. Familiarity with bug tracking systems like Jira, test management tools, and knowledge of software development lifecycles are commonly required, and a certification like ISTQB can be a plus. Strong analytical skills, effective communication, and a collaborative mindset help Manual QA Engineers identify issues and work effectively within development teams. These skills are crucial for ensuring software quality, minimizing defects, and supporting timely project delivery.

What does a manual QA engineer do?

A manual QA engineer tests software applications manually to identify bugs, ensure functionality, and verify that features meet requirements. They create test cases, execute test plans, document defects, and collaborate with developers to improve product quality, often using tools like test management software and following industry standards.
What are the most commonly searched types of Manual Qa Engineer jobs in Rochester, NY? The most popular types of Manual Qa Engineer jobs in Rochester, NY are:
What are popular job titles related to Manual Qa Engineer jobs in Rochester, NY? For Manual Qa Engineer jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Manual Qa Engineer jobs in Rochester, NY look for? The top searched job categories for Manual Qa Engineer jobs in Rochester, NY are:
Manual Qa Engineer jobs near you
Infographic showing various Manual Qa Engineer job openings in Rochester, NY as of July 2026, with employment types broken down into 89% Full Time, 8% Part Time, 1% Temporary, and 2% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $99,624 per year, or $47.9 per hour.

Quality Assurance Engineer

Stark Pharma Solutions Inc

Rochester, NY • On-site

Contractor

Posted 26 days ago

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Quality Assurance Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: Quality Assurance Engineer
Location: New York
Duration: Long Term

Position Overview

We are seeking an experienced Quality Assurance Engineer to support quality assurance activities within a pharmaceutical, biotechnology, or medical device manufacturing environment. This role will focus on ensuring product quality, regulatory compliance, and continuous process improvement by supporting quality systems, inspections, audits, documentation, and CAPA activities. The ideal candidate will have strong knowledge of FDA regulations, GMP, ISO standards, and quality management systems while collaborating with cross-functional teams to maintain the highest quality standards.

Key Responsibilities

• Perform quality inspections, manufacturing audits, and process reviews to ensure compliance with quality standards.

• Review batch records, device history records, and quality documentation for accuracy and regulatory compliance.

• Ensure compliance with FDA regulations, GMP, ISO 13485, and company quality management systems.

• Investigate quality issues, non-conformances, deviations, and customer complaints, and support CAPA activities.

• Participate in internal audits, supplier audits, and regulatory inspections while ensuring audit readiness.

• Collaborate with Manufacturing, Engineering, Regulatory Affairs, Validation, and Quality Control teams to improve product quality and manufacturing processes.

• Develop, review, and maintain quality procedures, SOPs, work instructions, and technical documentation.

• Support risk assessments, root cause analysis, change control, and continuous improvement initiatives.

• Monitor quality metrics and analyze trends to identify opportunities for process improvement and operational excellence.

• Ensure compliance with company quality policies and applicable regulatory requirements throughout the product lifecycle.

Required Qualifications

• Bachelor's Degree in Engineering, Biotechnology, Life Sciences, Chemistry, Biology, or a related scientific discipline.

• 2–5 years of Quality Assurance experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.

• Strong knowledge of FDA regulations, GMP, ISO 13485, CAPA, Quality Management Systems (QMS), and regulatory compliance requirements.

• Experience performing quality inspections, manufacturing audits, documentation review, and quality investigations.

• Hands-on experience with deviations, non-conformances, root cause analysis, CAPA, and change control processes.

• Familiarity with quality documentation, batch record review, SOP development, and document control systems.

• Experience supporting internal audits, supplier audits, and regulatory inspections.

• Strong analytical, problem-solving, technical documentation, and organizational skills.

• Excellent communication and cross-functional collaboration skills with the ability to work effectively in a regulated environment.

• Experience working within pharmaceutical, biotechnology, or medical device manufacturing facilities is highly preferred.

• Knowledge of statistical quality tools, risk management methodologies, Lean Manufacturing, or Six Sigma is an added advantage.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/