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Contract Manual Qa Engineer Jobs in Rochester, 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 ...

Quality Engineer II

Batavia, NY · On-site

$78K - $100K/yr

Quality Assurance Engineer Reports To: Quality Program Manager FLSA Status & EEO Code: Exempt ... Create, maintain, and distribute Quality Databooks (product history manual). * Resolve customer ...

Quality Engineer II

Batavia, NY · On-site

$78K - $100K/yr

Quality Assurance Engineer Reports To: Quality Program Manager FLSA Status & EEO Code: Exempt ... Create, maintain, and distribute Quality Databooks (product history manual). * Resolve customer ...

New

Quality Assurance Engineer Reports To: Quality Program Manager FLSA Status & EEO Code: Exempt ... Create, maintain, and distribute Quality Databooks (product history manual). * Resolve customer ...

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 ...

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 ...

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

Senior Specialist, Quality Engineering

Rochester, NY · On-site

$73K - $135K/yr

  • Medical

  • Retirement

  • PTO

Engineer manages and maintains program Quality Assurance activities, and routinely interfaces with Engineering, Management, Customers and Subcontractors. Individual will be heavily involved on-site ...

Software Quality Engineer

Rochester, NY · On-site +1

$61K - $97K/yr

  • PTO

Manual Testing Execution: Perform functional, exploratory, regression, and user acceptance testing ... Develop effective validation approaches, reusable QA coverage, and documentation based on business ...

QUALITY ENGINEER

Rochester, NY · On-site

$25 - $35/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Participate in contract review meetings to initiate and advise on inspection plans. * Utilize HQA ... Additional certification in Quality Assurance is a plus. JOB BENEFITS: * Vacation * Sick Days

Position: QA Test Analyst III Location: Rochester NY 14614 ( Only Local ) Duration: 3 -6 Months ... Bachelor's degree in computer science, computer engineering or relevant field required. 8-10 years ...

Quality Engineer

Rochester, NY · On-site

$50 - $55/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... Contract to hire opportunity. What We're Looking For: * Must know AS9102 and QA-01.1.1 First ... BA in Engineering or other technical discipline Preferred Skills: * Use Six Sigma & Lean concepts ...

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Contract Manual Qa Engineer information

See Rochester, NY salary details

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

As of Aug 17, 2026, the average hourly pay for contract 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 are the key skills and qualifications needed to thrive as a contract manual QA engineer?

To thrive as a Contract Manual QA Engineer, you need a solid understanding of software testing fundamentals, test case design, and defect reporting, usually backed by experience in QA or a related field. Familiarity with test management tools like JIRA, TestRail, or Zephyr and knowledge of various operating systems and browsers are commonly required. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate with development teams. These skills ensure thorough testing, accurate documentation, and timely delivery of high-quality software products.

What does a contract manual QA engineer do?

A Contract Manual QA Engineer is responsible for manually testing software applications to identify bugs, usability issues, and ensure that the product meets the specified requirements. Unlike automation testers, manual QA engineers perform testing without the use of automated tools, relying instead on test cases and user scenarios. As a contractor, they are hired for a specific project or time period, providing flexibility to companies that need short-term quality assurance support. Their work is crucial in maintaining software quality before release, often collaborating closely with development teams to resolve defects. They also document test results and help improve test processes.

What are some common challenges contract manual QA engineers face when joining new projects?

Contract Manual QA Engineers often encounter challenges such as quickly understanding unfamiliar codebases, adapting to different testing processes, and integrating with established teams. Since contracts are usually short-term, there’s a need to rapidly learn project requirements and company standards to ensure efficient testing from day one. Effective communication and proactive collaboration with developers, product managers, and other QA professionals are crucial for a smooth onboarding and for making an immediate impact on product quality.

What is the difference between Contract Manual Qa Engineer vs Contract Automation Qa Engineer?

AspectContract Manual Qa EngineerContract Automation Qa Engineer
CertificationsISTQB, CSQAISTQB, CSQA, Automation tools certifications
Work EnvironmentManual testing, test case executionAutomated testing, scripting, tool usage
Industry UsageCommon in industries with manual testing needsGrowing in tech-driven industries
Search IntentManual testing roles, QA testing jobsAutomation testing roles, QA automation jobs

The Contract Manual Qa Engineer primarily focuses on manual testing processes, executing test cases without automation tools. In contrast, the Contract Automation Qa Engineer specializes in developing and maintaining automated test scripts. Both roles require similar certifications and work in quality assurance environments, but their core responsibilities differ significantly, reflecting the shift towards automation in software testing.

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 Contract Manual Qa Engineer jobs in Rochester, NY?

For Contract Manual Qa Engineer jobs in Rochester, NY, the most frequently searched job titles are:

What cities near Rochester, NY are hiring for Contract Manual Qa Engineer jobs?

Cities near Rochester, NY with the most Contract Manual Qa Engineer job openings:

Infographic showing various Contract Manual Qa Engineer job openings in Rochester, NY as of August 2026, with employment types broken down into 66% Full Time, 17% Part Time, and 17% Contract. Highlights an 67% In-person, and 33% 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

Re-posted 16 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/