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60 Ipro Quality Assurance Engineer Jobs Hiring Near You

uAvionix

Quality Assurance Engineer

Columbia Falls, MT · On-site

Quality Assurance Engineer Department: Operations Reports To: Director of Quality Location: On-site; Columbia Falls, MT Position Type: Full Time, Salary, Exempt, IC3/IC4 Job Summary: The Quality ...

Wingbrace

Quality Assurance Engineer

Lincoln, MA · On-site

Software Quality Assurance Engineer Location -Onsite Hybrid role Lincoln Massachusetts About Wingbrace Wingbrace (www.wingbrace.com) is a software and technical services company focused on the ...

Pavago

Quality Assurance Engineer

Quality Assurance Engineer (Manual + Automation SaaS) - Remote Position Type: Full-Time, Remote Working Hours: U.S. Business Hours (flexible for releases & sprints) About the Role We're hiring a ...

FlowPlay, Inc.

QA Engineer

Seattle, WA · On-site

$110 - $120/hr

QA Engineer Job Summary We are seeking a collaborative and forward-thinking experienced QA Engineer to join our established QA team as our resident Automation Specialist. You will be joining a close ...

Vertex Sigma Software

QA Engineer

Foster City, CA

QA Engineer Onsite in Foster City, CA | 5 days in office The Quality Assurance team is actively seeking a Quality Assurance Engineer to help ensure that our backend services are optimized, secure ...

NR Consulting

QA Engineer

Sunnyvale, CA · Hybrid

Title: QA Engineer Location: Sunnyvale, CA or Austin, TX (3 days a week hybrid) Type: Contract Duration: long Term Description: * We are seeking a highly experienced Senior QA Engineer with 9+ years ...

THRONE LABS INC

QA Engineer

Los Angeles, CA · Remote

Software Quality Assurance Engineer FULL-TIME, WASHINGTON, D.C. About the job Throne aims to provide peace of mind to those that venture out each day -- making it so no one has to worry about finding ...

PSR Associates

Quality Assurance Engineer

Chicago, IL · Hybrid

QA Engineer Position Description We are seeking a QA Engineer to join our team. The selected candidate will work a hybrid schedule consisting of onsite workdays in Chicago, IL. Summary: The ideal ...

Burford Capital LLC

QA Engineer

Manhattan, NY · On-site

$100 - $120/hr

The QA Engineer will work as part of Burford's Core Services group and contribute to a variety of software and data projects across the firm's evolving tools and platforms. The individual will help ...

Lennar Homes

QA Engineer

Miami, FL · On-site

QA Engineer We are Lennar Lennar is one of the nation's leading homebuilders, dedicated to making an impact and creating an extraordinary experience for their Homeowners, Communities, and Associates ...

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Quality Assurance Engineer

Stark Pharma Solutions Inc

Rochester, NY • On-site

Contractor

Re-posted 21 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/