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Qa Engineer Resume Jobs (NOW HIRING)

ProScore Technologies

QA Engineer

Fort Lauderdale, FL · On-site

QA Engineer - Job Profile Location: Fort Lauderdale, FL We are seeking a QA Engineer to join our ... Submit your resume and a cover letter detailing your experience and why you're the ideal candidate ...

Edgewater Technical Associates

QA Engineer

Aiken, SC · On-site

Aiken, SC QA Engineer- QA Engineer will support a multi-year construction project involving ... resume without first having detailed discussions with you and obtaining your permission to do so.

Fiserv, Inc.

Quality Assurance Engineer

Milwaukee, WI · On-site

Quality Assurance Engineer EMPLOYER: Fiserv Solutions, LLC LOCATION: Milwaukee, WI (and various ... Apply by selecting "Apply" on this page and following prompts to attach resume and submit. JOB CODE:

MarginPoint

Quality Assurance Engineer

Laguna Hills, CA · On-site

$100 - $125/hr

The QA Engineer needs to be intimately familiar with Microsoft technologies and have had previous ... and resume verification. The Position located in Laguna Hills, CA. No relocation provided.

AxisCare

QA Engineer

Waco, TX · On-site

- QA Engineer Reports to - Director of QA PositionSummary We are seeking a skilled and detail ... a brief resume and either a written or video cover letter. We review the cover letter before ...

Amicis Global

QA Engineer

Seattle, WA · On-site

Title: Web Quality Assurance Engineer (Multiple Positions) Location: Seattle, WA (Onsite) Duration: 6+ Months Key job responsibilities * You'll build and maintain test infrastructure for a web ...

AxisCare

QA Engineer

Waco, TX · On-site

- QA Engineer Reports to - Director of QA Position Summary We are seeking a skilled and detail ... a brief resume and either a written or video cover letter. We review the cover letter before ...

NAVA Software Solutions

QA Engineer

Houston, TX · On-site

NAVA Software solutions is looking for a QA Engineer Details: QA Engineer Location: Houston, TX (2-3 days Onsite) Duration: 6-12 months Client is looking for a QA having strong exp in SQL / for BI ...

Rectangle Health

QA Engineer

White Plains, NY

$90K - $115K/yr

QA Engineer At Rectangle Health, we believe that our team members are our most important asset. We grow our team by hiring best-in-class talent. We encourage all employees to contribute their ...

Rectangle Health

QA Engineer

White Plains, NY · On-site

$90K - $115K/yr

QA Engineer At Rectangle Health, we believe that our team members are our most important asset. We grow our team by hiring best-in-class talent. We encourage all employees to contribute their ...

Black Creek Integrated Systems

Be Seen First

Quality Assurance Engineer

Irondale, AL · On-site

$75K - $90K/yr

The QA Engineer has the authority and responsibility to accept or reject work items before they count toward sprint acceptance. Our product portfolio includes legacy applications with limited ...

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As of Sep 8, 2026, the average hourly pay for qa engineer resume in the United States is $48.54, according to ZipRecruiter salary data. Most workers in this role earn between $38.22 and $55.53 per hour, depending on experience, location, and employer.

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Quality Assurance Engineer

Stark Pharma Solutions Inc

Rochester, NY • On-site

Contractor

Re-posted 9 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/