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Quality Assurance Engineer Manager Jobs in Rochester, NY

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 ...

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 ...

groteindustries

Quality Assurance Manager

Avon, NY · On-site

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 ...

ADDSOURCE

QA Automation Manager

Rochester, NY · On-site

Minimum 10+ Years We are looking for an QA Automation Manager to lead quality engineering initiatives within a highly regulated healthcare and medical device environment. The ideal candidate will ...

Unifin SAS

Quality Assurance Manager

Rochester, NY · On-site

Quality Assurance Manager Who we are? As a French pharmaceutical industrial group, we strive to make healthcare solutions that improve and simplify patients' lives accessible to as many people as ...

Unifin SAS

Quality Assurance Manager

Rochester, NY · On-site

Quality Assurance oversight of Deviation Management system. Technical Complaint Management: Investigation, documentation and approval of technical complaints and adverse events. (Adverse events at ...

Collabera

Quality Assurance

Rochester, NY · On-site

Reports progress on problem resolution to management. Implements pre-determined improvements to ... Performs work flow analysis and recommends quality improvements. * Escalates software process ...

Baldwin Richardson Foods

QA Analyst

Williamson, NY · On-site

Performs perfect package checks on applicable productions lines and reports any issues to QA management * Verifies food safety preventive controls are in place and operating properly * Supports and ...

Cooper Companies

QA Technician

West Henrietta, NY · On-site

$22.90 - $27.89/hr

The Quality Assurance Technician will be responsible for auditing Packaging finished goods, as well ... Performs audits as directed by management that include, but are not limited to: * a. DHR (device ...

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Quality Assurance Engineer Manager information

What does a Quality Assurance Engineer Manager do?

A Quality Assurance (QA) Engineer Manager oversees the quality assurance process within a company to ensure that products or services meet specific standards of quality. They lead and mentor QA teams, develop testing strategies, and coordinate with other departments to identify and resolve quality issues. Their responsibilities also include setting quality goals, implementing best practices, and ensuring compliance with industry regulations. By managing the quality assurance process, they help prevent defects, improve customer satisfaction, and support the overall success of the organization.

What are the key skills and qualifications needed to thrive as a Quality Assurance Engineer Manager?

To thrive as a Quality Assurance Engineer Manager, you need a strong background in software testing methodologies, quality standards, and team leadership, often supported by a degree in computer science or a related field. Familiarity with automation tools (like Selenium or JIRA), test management systems, and relevant certifications (such as ISTQB) is essential. Strong communication, problem-solving, and organizational skills help foster collaboration and drive continuous improvement. These competencies ensure the delivery of high-quality products, efficient processes, and effective team performance.

How does a Quality Assurance Engineer Manager typically collaborate with cross-functional teams to ensure product quality?

A Quality Assurance Engineer Manager works closely with development, product management, and operations teams to establish clear quality standards and testing protocols. They often facilitate regular meetings to align on project goals, address potential quality risks, and coordinate testing timelines. Effective QA managers foster open communication, ensuring that feedback from QA is integrated into the development process early and often. This collaborative approach helps prevent defects, streamlines releases, and promotes a culture of shared responsibility for product quality.

What is the difference between Quality Assurance Engineer Manager vs Quality Assurance Engineer?

AspectQuality Assurance Engineer ManagerQuality Assurance Engineer
CredentialsBachelor's degree in Computer Science or related field; often managerial certificationsBachelor's degree in Computer Science, Engineering, or related field
Work EnvironmentLeads QA teams, manages testing strategies, collaborates with managementPerforms testing, executes test cases, reports bugs
Employer & Industry UsageUsed in organizations with dedicated QA teams, in software, manufacturing, techEntry to mid-level roles in similar industries, focused on testing tasks

The main difference is that the Quality Assurance Engineer Manager oversees QA teams and strategies, while the Quality Assurance Engineer focuses on executing tests and identifying issues. The manager role involves leadership and planning, whereas the engineer role is more hands-on with testing activities.

What are the most commonly searched types of Quality Assurance Engineer jobs in Rochester, NY? The most popular types of Quality Assurance Engineer jobs in Rochester, NY are:
What are popular job titles related to Quality Assurance Engineer Manager jobs in Rochester, NY? For Quality Assurance Engineer Manager jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Quality Assurance Engineer Manager jobs in Rochester, NY look for? The top searched job categories for Quality Assurance Engineer Manager jobs in Rochester, NY are:
What cities near Rochester, NY are hiring for Quality Assurance Engineer Manager jobs? Cities near Rochester, NY with the most Quality Assurance Engineer Manager job openings:
Quality Assurance Engineer Manager jobs near you
Infographic showing various Quality Assurance Engineer Manager job openings in Rochester, NY as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution.

Quality Assurance Engineer

Stark Pharma Solutions Inc

Rochester, NY • On-site

Contractor

Re-posted 10 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/