ZipRecruiter

Log In

1

From Home Manual Qa Engineer Jobs in Rochester, NY

Graham Corporation

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 ...

Graham Manufacturing

Quality Engineer II

Batavia, NY

$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 ...

Graham Manufacturing

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 ...

groteindustries

Quality Assurance Manager

Avon, NY · On-site

From durable, easy to see stop lights to the latest in LED lighting technology, Grote has been ... Bachelor's degree in Quality Engineering, Engineering, Business, or other related field of study.

Grote Industries

Quality Assurance Manager

Avon, NY · On-site

$105K - $120K/yr

From durable, easy to see stop lights to the latest in LED lighting technology, Grote has been ... Bachelor's degree in Quality Engineering, Engineering, Business, or other related field of study.

Collabera

Quality Assurance

Rochester, NY · On-site

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

Mindlance

Quality Assurance Specialist

Rochester, NY · On-site

W2 Hybrid Temp to hire job position Notes from hiring manager: Need someone with Shop Floor level ... At least 5 years in Quality Assurance/Aseptic Manufacturing Operations Management; 3 years in ...

New

General Motors

Quality Assurance Lead

Rochester, NY · On-site

$88K - $140K/yr

This role partners closely with Manufacturing, Quality Engineering, Product Engineering ... Benefits Overview From day one, we're looking out for your well-being-at work and at home-so you ...

General Motors

Quality Assurance Lead

Rochester, NY · On-site

$88K - $140K/yr

This role partners closely with Manufacturing, Quality Engineering, Product Engineering ... Benefits Overview From day one, we're looking out for your well-being-at work and at home-so you ...

General Motors

Quality Assurance Lead

Rochester, NY · On-site

$88K - $140K/yr

This role partners closely with Manufacturing, Quality Engineering, Product Engineering ... Benefits Overview From day one, we're looking out for your well-being-at work and at home-so you ...

General Motors

Quality Assurance Lead

Rochester, NY

$88K - $140K/yr

This role partners closely with Manufacturing, Quality Engineering, Product Engineering ... Benefits Overview From day one, we're looking out for your well-being-at work and at home-so you ...

next page

Showing results 1-20

All JobsManual Qa Engineer JobsFrom Home Manual Qa Engineer JobsFrom Home Manual Qa Engineer Jobs in Rochester, NY

From Home Manual Qa Engineer information

See Rochester, NY salary details

$18

$47

$77

How much do from home manual qa engineer jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for from home 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 from home manual QA engineer?

A From Home Manual QA Engineer is a quality assurance professional who works remotely to test software applications manually. They are responsible for identifying bugs, reporting issues, and ensuring that the software meets specified requirements without using automated testing tools. These engineers communicate with development teams, create and execute test cases, and help maintain product quality from their home office. Their work is crucial to delivering reliable software products to end users.

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

To thrive as a From Home Manual QA Engineer, you need a solid understanding of software testing methodologies, bug tracking, and quality assurance processes, often supported by a degree in computer science or a related field. Familiarity with tools like Jira, TestRail, and various web or mobile platforms is typically required, and ISTQB certification is a plus. Attention to detail, strong analytical thinking, and effective communication are crucial soft skills for identifying issues and collaborating with remote teams. These skills ensure accurate testing, timely defect resolution, and high-quality product delivery in a remote work environment.

What are some common challenges faced by manual QA engineers working from home, and how can they be addressed?

Manual QA engineers working remotely may encounter challenges such as maintaining clear communication with development teams, accessing necessary testing environments, and managing distractions at home. To address these issues, it's important to establish regular check-ins with team members, use collaboration tools like Slack or Jira, and ensure secure remote access to testing platforms. Creating a dedicated workspace and a structured daily routine can also help improve focus and productivity.

What is the difference between From Home Manual Qa Engineer vs From Home Automation Qa Engineer?

AspectFrom Home Manual Qa EngineerFrom Home Automation Qa Engineer
CertificationsBasic QA certifications (ISTQB, CSQA)Same as Manual QA, plus automation tools certifications (Selenium, QTP)
Work EnvironmentPrimarily manual testing, test case executionManual testing plus automation script development and execution
Industry UsageCommon across various industries for manual testing needsMore prevalent in tech and software companies focusing on automation

From Home Manual Qa Engineers focus on manual testing processes, executing test cases without automation tools. In contrast, From Home Automation Qa Engineers combine manual testing with automation scripting to improve testing efficiency. Both roles often work remotely and require similar foundational QA skills, but automation engineers need additional technical expertise in scripting and automation tools.

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 From Home Manual Qa Engineer jobs in Rochester, NY?

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

What job categories do people searching From Home Manual Qa Engineer jobs in Rochester, NY look for?

The top searched job categories for From Home Manual Qa Engineer jobs in Rochester, NY are:

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

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

From Home Manual Qa Engineer jobs near you

Quality Assurance Engineer

Stark Pharma Solutions Inc

Rochester, NY • On-site

Contractor

Re-posted 7 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/