Quality Assurance (QA) Engineer / Senior QA Specialist (TEST) Experience Required: 7-10 Years ... investigations, performing root cause analysis, assessing product impact, and ensuring timely ...
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Quality Assurance (QA) Engineer / Senior QA Specialist (TEST) Experience Required: 7-10 Years ... investigations, performing root cause analysis, assessing product impact, and ensuring timely ...
Quick apply
Quality Assurance (QA) Engineer / Senior QA Specialist (TEST) Experience Required: 7-10 Years ... investigations, performing root cause analysis, assessing product impact, and ensuring timely ...
Hollywood, MD · On-site
$75 - $90/hr
This role leads root cause investigations, supports continuous improvement initiatives, and drives data driven trend analysis and response activities. The Quality Assurance Engineer partners closely ...
Hollywood, MD · On-site
$75 - $90/hr
This role leads root cause investigations, supports continuous improvement initiatives, and drives data driven trend analysis and response activities. The Quality Assurance Engineer partners closely ...
Juncos, PR · On-site
$90 - $130/hr
Lead and document investigations , root cause analyses, and CAPA development * Lead and support ... Serve as QA Manager designee on the local Change Control Review Board (CCRB) * Review and approve ...
Juncos, PR · On-site
$90 - $130/hr
Lead and document investigations , root cause analyses, and CAPA development * Lead and support ... Serve as QA Manager designee on the local Change Control Review Board (CCRB) * Review and approve ...
Pittsburgh, PA · On-site
$65K - $85K/yr
Job Title: Site Quality Assurance Manager (Site QA) FLSA Status: Non-Exempt Position Type ... Initiate and complete CAPA investigation as deemed necessary and report results and trends.
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Pittsburgh, PA · On-site
$65K - $85K/yr
Job Title: Site Quality Assurance Manager (Site QA) FLSA Status: Non-Exempt Position Type ... Initiate and complete CAPA investigation as deemed necessary and report results and trends.
Hollywood, MD · On-site
$75K - $90K/yr
This role leads root cause investigations, supports continuous improvement initiatives, and drives data driven trend analysis and response activities. The Quality Assurance Engineer partners closely ...
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Hollywood, MD · On-site
$75K - $90K/yr
This role leads root cause investigations, supports continuous improvement initiatives, and drives data driven trend analysis and response activities. The Quality Assurance Engineer partners closely ...
Los Angeles, CA · On-site
The QA Specialist is responsible for product quality by evaluating various processes against ... Investigate and report as required, issues identified under the deviation management system ...
Los Angeles, CA · On-site
The QA Specialist is responsible for product quality by evaluating various processes against ... Investigate and report as required, issues identified under the deviation management system ...
Los Angeles, CA · On-site
The QA Specialist is responsible for product quality by evaluating various processes against ... Investigate and report as required, issues identified under the deviation management system ...
Los Angeles, CA · On-site
The QA Specialist is responsible for product quality by evaluating various processes against ... Investigate and report as required, issues identified under the deviation management system ...
The QA Manager requires the ability to evaluate, investigate, solve problems, and respond to quality-related questions and requests in a deadline-controlled environment. This position is responsible ...
The QA Manager requires the ability to evaluate, investigate, solve problems, and respond to quality-related questions and requests in a deadline-controlled environment. This position is responsible ...
Fort Lauderdale, FL · On-site
$20 - $21/hr
The Quality Assurance Associate is responsible for planning, developing, implementing, and ... Conducts initial liability claims investigations when needed * Performs other related work as ...
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Fort Lauderdale, FL · On-site
$20 - $21/hr
The Quality Assurance Associate is responsible for planning, developing, implementing, and ... Conducts initial liability claims investigations when needed * Performs other related work as ...
Fort Lauderdale, FL · On-site
$20 - $21/hr
The Quality Assurance Associate is responsible for planning, developing, implementing, and ... Conducts initial liability claims investigations when needed * Performs other related work as ...
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Fort Lauderdale, FL · On-site
$20 - $21/hr
The Quality Assurance Associate is responsible for planning, developing, implementing, and ... Conducts initial liability claims investigations when needed * Performs other related work as ...
Manhattan, NY · On-site
$8.7K/mo
Purpose The Manager, Quality Assurance (QA), Global AML - US leads and contributes to the ... Assess the quality, completeness, accuracy, and consistency of investigations, risk assessments ...
Manhattan, NY · On-site
$8.7K/mo
Purpose The Manager, Quality Assurance (QA), Global AML - US leads and contributes to the ... Assess the quality, completeness, accuracy, and consistency of investigations, risk assessments ...
You will conduct shop investigations, special quality assurance investigations, failure analysis investigations, audits and studies to identify problems underlying causes. * You will collect, monitor ...
You will conduct shop investigations, special quality assurance investigations, failure analysis investigations, audits and studies to identify problems underlying causes. * You will collect, monitor ...
Los Angeles, CA · On-site
The QA Specialist is responsible for product quality by evaluating various processes against ... Investigate and report as required, issues identified under the deviation management system ...
Los Angeles, CA · On-site
The QA Specialist is responsible for product quality by evaluating various processes against ... Investigate and report as required, issues identified under the deviation management system ...
Los Angeles, CA · On-site
The QA Specialist is responsible for product quality by evaluating various processes against ... Investigate and report as required, issues identified under the deviation management system ...
Los Angeles, CA · On-site
The QA Specialist is responsible for product quality by evaluating various processes against ... Investigate and report as required, issues identified under the deviation management system ...
Florham Park, NJ · On-site
$90K - $115K/yr
Handles product-related quality events, including change controls, investigations, OOS/OOT events ... Serves as a QA/QMS approver for controlled documents, including SOPs, work instructions, forms, and ...
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Florham Park, NJ · On-site
$90K - $115K/yr
Handles product-related quality events, including change controls, investigations, OOS/OOT events ... Serves as a QA/QMS approver for controlled documents, including SOPs, work instructions, forms, and ...
Wilmington, DE · On-site
$70 - $100/hr
... investigating compliance concerns, and identifying opportunities for process improvement. Key ... Quality Assurance Reviews and Audits * Maintains current knowledge of federal, state, payer, and ...
New
Wilmington, DE · On-site
$70 - $100/hr
... investigating compliance concerns, and identifying opportunities for process improvement. Key ... Quality Assurance Reviews and Audits * Maintains current knowledge of federal, state, payer, and ...
New
Manhattan, NY · On-site
$8.7K/mo
... of financial crime investigations and risk assessments, and oversight of quality assurance ... governance, reporting, and continuous improvement initiatives. What You'll Do • Perform ...
Manhattan, NY · On-site
$8.7K/mo
... of financial crime investigations and risk assessments, and oversight of quality assurance ... governance, reporting, and continuous improvement initiatives. What You'll Do • Perform ...
Vista, CA · On-site
$75 - $90/hr
Conduct investigations concerning operational problems, customer complaints, non-conformances, failures, and/or any other quality investigations; the QA supervisor is responsible for performing ...
Vista, CA · On-site
$75 - $90/hr
Conduct investigations concerning operational problems, customer complaints, non-conformances, failures, and/or any other quality investigations; the QA supervisor is responsible for performing ...
Florham Park, NJ · On-site
$90K - $115K/yr
Handles product-related quality events, including change controls, investigations, OOS/OOT events ... Serves as a QA/QMS approver for controlled documents, including SOPs, work instructions, forms, and ...
Florham Park, NJ · On-site
$90K - $115K/yr
Handles product-related quality events, including change controls, investigations, OOS/OOT events ... Serves as a QA/QMS approver for controlled documents, including SOPs, work instructions, forms, and ...
... investigating compliance concerns, and identifying opportunities for process improvement. Key ... Quality Assurance Reviews and Audits * Maintains current knowledge of federal, state, payer, and ...
... investigating compliance concerns, and identifying opportunities for process improvement. Key ... Quality Assurance Reviews and Audits * Maintains current knowledge of federal, state, payer, and ...
$32K - $41K
7% of jobs
$41K - $50K
14% of jobs
$51.5K is the 25th percentile. Wages below this are outliers.
$50K - $59K
24% of jobs
The median wage is $63.5K / yr.
$59K - $68K
9% of jobs
$68K - $77K
5% of jobs
$77K - $86K
15% of jobs
$86.8K is the 75th percentile. Wages above this are outliers.
$86K - $95K
3% of jobs
$95K - $104K
6% of jobs
$104K - $113K
4% of jobs
$113K - $122K
12% of jobs
$122K - $131K
0% of jobs
$32K
$75.3K
$131K
Cities with the most Qa Investigator job openings:
States with the most job openings for Qa Investigator jobs include:

Raleigh, NC • On-site
Contractor
Re-posted 11 days ago
Quality Assurance (QA) Engineer / Senior QA Specialist (TEST)
Experience Required: 7–10 Years
Location: Raleigh, NC
Visa: US Citizen / Green Card
Mode of Work: In-office
Duration: 10 to 12 months +
Role Overview
The QA Engineer / Senior QA Specialist will provide experienced, hands-on quality oversight for commercial GMP manufacturing operations. This role requires strong judgment, deep knowledge of GMP regulations, and the ability to independently manage quality events while partnering closely with Manufacturing, Validation, and Engineering teams in a regulated environment.
Key Responsibilities
* Provide independent QA oversight for commercial GMP manufacturing operations in compliance with 21 CFR Parts 210/211, EU GMP, and ICH Q10.
* Own and manage deviations, CAPAs, and change controls in TrackWise, including leading investigations, performing root cause analysis, assessing product impact, and ensuring timely, effective closure.
* Review and approve validation and qualification documentation (including IQ/OQ/PQ, protocols, reports, and summary documentation) using Kneat, ensuring compliance with GMP, data integrity, and regulatory expectations.
* Perform thorough batch record review and release support, identifying trends, risks, and opportunities for process improvement.
* Support equipment lifecycle activities, including maintenance, calibration, and qualification, through review of GMP documentation and records in CMMS.
* Review, approve, and maintain controlled documents, SOPs, and training records in Veeva Vault, ensuring accuracy, compliance, and inspection readiness.
* Contribute to the development, revision, and continuous improvement of QA procedures, processes, and documentation to support operational readiness and manufacturing excellence in a cGMP facility.
* Serve as a QA point of contact for manufacturing operations, providing guidance on GMP expectations, deviation handling, and change implementation.
* Support regulatory inspections, internal audits, and customer audits, including preparation, participation, and follow-up actions.
* Mentor junior QA team members and provide guidance on GMP best practices, as needed.
Systems & Tools
* TrackWise – Deviations, CAPAs, Change Control
* Kneat – Validation, Qualification, Batch Record Review
* Veeva Vault – Document and Training Management
* CMMS – Equipment Maintenance and Calibration Records
Qualifications
* Bachelor’s degree in Science, Engineering, or a related discipline (or equivalent experience).
* 7–10 years of Quality Assurance experience in a cGMP-regulated environment (pharmaceutical, biotech, or related industry).
* Strong working knowledge of FDA, EU, and ICH GMP regulations.
* Proven experience independently managing quality investigations, change controls, and validation documentation.
* Experience supporting commercial manufacturing operations.
* Strong communication, documentation, and cross-functional collaboration skills.
* Demonstrated ability to work independently while balancing multiple priorities in a fast-paced GMP environment
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Recruiting and staffing services
1 - 10 Employees
Northville, MI, US
2021