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Quality Assurance Engineer Playwright Jobs in Rochester, NY

Graham Corporation

Quality Engineer II

Batavia, NY · On-site

$78K - $100K/yr

Job Title: Quality Assurance Engineer Reports To: Quality Program Manager FLSA Status & EEO Code: Exempt/Professional Division/Department: Quality Level of Work: Level II Position Summary: The ...

Graham Manufacturing

Quality Engineer II

Batavia, NY · On-site

$68K - $88K/yr

Job Title: Quality Assurance Engineer Reports To: Quality Program Manager FLSA Status & EEO Code: Exempt/Professional Division/Department: Quality Level of Work: Level II Position Summary: The ...

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/Professional Division/Department: Quality Level of Work: Level II Position Summary: The Quality Assurance ...

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 · 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 ...

Butler/Till, Inc.

Software Quality Engineer

Rochester, NY · On-site +1

$61K - $97K/yr

Develop effective validation approaches, reusable QA coverage, and documentation based on business ... Cypress, Playwright, or similar technologies. PREFERRED- * Experience with SQL for database ...

SA Technologies Inc.

QA Test Analyst III

Rochester, NY · On-site

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 ...

Syntec Optics

Quality Engineer

Rochester, NY · On-site

$71K - $91K/yr

Conduct Quality Assurance audits and routine checks, tests, gauging and instrument inspections of ... Experience with operating or programming a Sheffield or Zeiss CMM preferred. * Strong attention to ...

Assa Abloy

Manager of Corporate Quality

Rochester, NY · On-site

$100K - $120K/yr

... QA Engineering insource or outsource implementation. * Proactive with Customers: First point of contact for customer issues * Improve and assure documented procedures. * Value Added Value Engineering ...

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As of Aug 27, 2026, the average hourly pay for quality assurance engineer playwright 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.

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Quality Assurance Engineer

Rochester, NY • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-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/