The QA Auditor will ensure the accuracy, integrity, and compliance of toxicological research ... The successful candidate will be independent, accountable, and able to deliver polished, GLP ...
The QA Auditor will ensure the accuracy, integrity, and compliance of toxicological research ... The successful candidate will be independent, accountable, and able to deliver polished, GLP ...
QA Manager
Exton, PA · On-site
Quality Assurance (QA) Specialist / Manager - DMPK Location: Exton, PA Department: DMPK (Drug ... Ensure compliance with GLP regulations, company SOPs, client requirements, and industry best ...
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QA Manager
Exton, PA · On-site
Quality Assurance (QA) Specialist / Manager - DMPK Location: Exton, PA Department: DMPK (Drug ... Ensure compliance with GLP regulations, company SOPs, client requirements, and industry best ...
Senior QA Auditor
Everett, WA · On-site
$80K - $87K/yr
Audits all disciplines (examples of disciplines include Method Validations, Non- Clinical GLP ... Autonomously performs SOP QA review, client hosting, regulatory agency hosting and external test ...
Senior QA Auditor
Everett, WA · On-site
$80K - $87K/yr
Audits all disciplines (examples of disciplines include Method Validations, Non- Clinical GLP ... Autonomously performs SOP QA review, client hosting, regulatory agency hosting and external test ...
Manager, Pre‑Clinical & Clinical Compliance
Raynham, MA · On-site
$37.75 - $50.50/hr
The Role In the role as Clinical and Pre-Clinical QA Compliance Manager, GCP Quality activities include GCP Clinical and GLP Preclinical audits will include the following: * Preparation prior to the ...
Manager, Pre‑Clinical & Clinical Compliance
Raynham, MA · On-site
$37.75 - $50.50/hr
The Role In the role as Clinical and Pre-Clinical QA Compliance Manager, GCP Quality activities include GCP Clinical and GLP Preclinical audits will include the following: * Preparation prior to the ...
QUALITY ASSURANCE TECH 3rd Shift Openings in Shenandoah. LLOYD, Inc. has an immediate opening for a ... the GLP Regulations of the FDA and the Corporate Operating Procedures. Requirements include ...
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QUALITY ASSURANCE TECH 3rd Shift Openings in Shenandoah. LLOYD, Inc. has an immediate opening for a ... the GLP Regulations of the FDA and the Corporate Operating Procedures. Requirements include ...
$75K - $90K/yr
Expert knowledge of GLP, GMP, and regulatory frameworks Management & Leadership * Train and develop QA team on data analysis and quality management * Strong interpersonal and relationship-building ...
$75K - $90K/yr
Expert knowledge of GLP, GMP, and regulatory frameworks Management & Leadership * Train and develop QA team on data analysis and quality management * Strong interpersonal and relationship-building ...
Quality Engineer
West Chester, OH · On-site
$67K - $87K/yr
Customer relations, supplier quality, improvement of existing products, introduction of new products, process development and/or improvement, GLP Quality Assurance Unit (QAU), and GLP Archiving. Key ...
Quality Engineer
West Chester, OH · On-site
$67K - $87K/yr
Customer relations, supplier quality, improvement of existing products, introduction of new products, process development and/or improvement, GLP Quality Assurance Unit (QAU), and GLP Archiving. Key ...
Quality Assurance Lead
Knoxville, TN · On-site
$75K - $90K/yr
Expert knowledge of GLP, GMP, and regulatory frameworks Management & Leadership * Train and develop QA team on data analysis and quality management * Strong interpersonal and relationship-building ...
Quality Assurance Lead
Knoxville, TN · On-site
$75K - $90K/yr
Expert knowledge of GLP, GMP, and regulatory frameworks Management & Leadership * Train and develop QA team on data analysis and quality management * Strong interpersonal and relationship-building ...
Primarily responsible for ensuring adherence to GLP regulations and developing an organizational model for the global Quality Assurance Unit. Manage a team of audit professionals responsible for ...
Primarily responsible for ensuring adherence to GLP regulations and developing an organizational model for the global Quality Assurance Unit. Manage a team of audit professionals responsible for ...
Director, Quality Assurance
Pasadena, CA · On-site
GMP/GLP Supplier Quality Management * Responsible for the end-to-end supplier qualification ... Serve as the primary QA point of contact for Xencor's contracted QP service provider(s) and EU/UK ...
Director, Quality Assurance
Pasadena, CA · On-site
GMP/GLP Supplier Quality Management * Responsible for the end-to-end supplier qualification ... Serve as the primary QA point of contact for Xencor's contracted QP service provider(s) and EU/UK ...
This Clinical Quality Assurance Senior Leader provides strategic leadership and operational ... Good Laboratory Practices (GLP), Good Clinical Practices (GCPs), and Good Pharmacovigilance ...
This Clinical Quality Assurance Senior Leader provides strategic leadership and operational ... Good Laboratory Practices (GLP), Good Clinical Practices (GCPs), and Good Pharmacovigilance ...
Ensure all GMP, GLP, GCP operations are in compliance , Establish training and audit programs, as ... Be responsible for release or rejection of GMP materials and utilize QA staff to manage the ...
Ensure all GMP, GLP, GCP operations are in compliance , Establish training and audit programs, as ... Be responsible for release or rejection of GMP materials and utilize QA staff to manage the ...
Supports the QA-to-QA relationship with key client(s) * Delivery of training in performance of ... GLP/GCP regulatory environment. * 2 years of Auditing experience * Postgraduate degree (MSC or ...
Supports the QA-to-QA relationship with key client(s) * Delivery of training in performance of ... GLP/GCP regulatory environment. * 2 years of Auditing experience * Postgraduate degree (MSC or ...
Senior Director, Global GMP Quality Assurance
South San Francisco, CA · On-site
$240K - $300K/yr
Serve as the functional leader for GLP/GMP Quality Assurance and a key member of the Quality Leadership Team, providing strategic direction and oversight for quality activities across nonclinical, ...
Senior Director, Global GMP Quality Assurance
South San Francisco, CA · On-site
$240K - $300K/yr
Serve as the functional leader for GLP/GMP Quality Assurance and a key member of the Quality Leadership Team, providing strategic direction and oversight for quality activities across nonclinical, ...
Supports the QA-to-QA relationship with key client(s) * Delivery of training in performance of ... GLP/GCP regulatory environment. * 2 years of Auditing experience * Postgraduate degree (MSC or ...
Supports the QA-to-QA relationship with key client(s) * Delivery of training in performance of ... GLP/GCP regulatory environment. * 2 years of Auditing experience * Postgraduate degree (MSC or ...
Serve as the functional leader for GLP/GMP Quality Assurance and a key member of the Quality Leadership Team, providing strategic direction and oversight for quality activities across nonclinical, ...
Serve as the functional leader for GLP/GMP Quality Assurance and a key member of the Quality Leadership Team, providing strategic direction and oversight for quality activities across nonclinical, ...
Additionally, they will be responsible for providing QA oversight of Quality Control (QC) activities to ensure compliance with applicable regulatory requirements (e.g., GMP, GLP) and internal quality ...
Additionally, they will be responsible for providing QA oversight of Quality Control (QC) activities to ensure compliance with applicable regulatory requirements (e.g., GMP, GLP) and internal quality ...
QA/RA Specialist
Dallas, TX · On-site
Develop, review, and maintain quality assurance and regulatory affairs documentation in compliance with GLP and GMP standards. * Ensure adherence to regulatory requirements from FDA, EMA, and other ...
QA/RA Specialist
Dallas, TX · On-site
Develop, review, and maintain quality assurance and regulatory affairs documentation in compliance with GLP and GMP standards. * Ensure adherence to regulatory requirements from FDA, EMA, and other ...
Specialist, Quality Assurance
Memphis, TN · On-site
Knowledge of CAP, CLIA, GLP and ISO standards and regulations. * Basic theoretical and operational job knowledge in quality assurance and laboratory operations. * Knowledge of organizational ...
Specialist, Quality Assurance
Memphis, TN · On-site
Knowledge of CAP, CLIA, GLP and ISO standards and regulations. * Basic theoretical and operational job knowledge in quality assurance and laboratory operations. * Knowledge of organizational ...
Quality Assurance Associate - R&D Quality Assurance As a Quality Assurance Associate - R&D Quality ... In this role, you will help advance GLP compliance, quality systems oversight, and audit readiness ...
Quality Assurance Associate - R&D Quality Assurance As a Quality Assurance Associate - R&D Quality ... In this role, you will help advance GLP compliance, quality systems oversight, and audit readiness ...
Glp Qa information
See salary details
$38K - $50.8K
3% of jobs
$50.8K - $63.6K
6% of jobs
$63.6K - $76.5K
11% of jobs
$82K is the 25th percentile. Wages below this are outliers.
$76.5K - $89.3K
12% of jobs
$89.3K - $102.1K
11% of jobs
The median wage is $114.1K / yr.
$102.1K - $114.9K
8% of jobs
$114.9K - $127.7K
4% of jobs
$137.2K is the 75th percentile. Wages above this are outliers.
$127.7K - $140.5K
27% of jobs
$140.5K - $153.4K
1% of jobs
$153.4K - $166.2K
1% of jobs
$166.2K - $179K
16% of jobs
$38K
$118.1K
$179K
How much do glp qa jobs pay per year?
What is a GLP QA?
A GLP QA (Good Laboratory Practice Quality Assurance) job involves ensuring compliance with GLP regulations in a laboratory setting. GLP QA professionals monitor study procedures, audit data, and verify that documentation meets regulatory standards. Their role helps ensure the integrity, reliability, and consistency of non-clinical laboratory studies, often for regulatory submissions. They work closely with scientists, management, and regulatory agencies to uphold quality standards.
What does a GLP QA do?
As a GLP QA professional, your daily tasks may involve reviewing study protocols, conducting in-process and final audits, and ensuring that all laboratory processes comply with Good Laboratory Practice standards. You will work closely with laboratory staff, scientists, and management to identify and resolve compliance issues and participate in training initiatives. Additionally, documenting audit findings, preparing quality reports, and contributing to continuous improvement initiatives are common parts of the role. This position requires both independent review work and close collaboration with cross-functional teams to maintain the highest standards of data integrity and regulatory compliance.
What skills and qualifications are needed to thrive as a GLP QA?
To excel as a GLP QA (Good Laboratory Practice Quality Assurance) professional, you should have a strong background in laboratory sciences, knowledge of GLP regulations, and experience with quality assurance processes. Familiarity with auditing tools, electronic data capture systems, and relevant certifications such as RQAP-GLP are often required. Excellent attention to detail, critical thinking, and strong communication skills are highly valued in this role. These competencies are essential to ensure compliance, accuracy, and integrity in non-clinical laboratory studies, which support regulatory submissions.
What cities are hiring for Glp Qa jobs?
Cities with the most Glp Qa job openings:
What are the most commonly searched types of Glp Qa jobs?
The most popular types of Glp Qa jobs are:
What states have the most Glp Qa jobs?
States with the most job openings for Glp Qa jobs include:
What job categories do people searching Glp Qa jobs look for?
The top searched job categories for Glp Qa jobs are:
- Full Time Ivr Qa Tester
- Aviation Quality Assurance Manager
- Quality Assurance Biotech
- Gcp Quality Assurance
- Software Qa Engineer 2
- Quality Assurance Manager Aerospace
- Mto Qa Validation Salary Pharma
- Solar Farms Quality Assurance Quality Control
- Contract Quality Assurance Batch Record Review
- Quality Assurance Shop Floor

Full-time
This job post has expired today. Applications are no longer accepted.
Key responsibilities
Conduct QA audits of toxicology study reports, laboratory data, pathology tables, electronic records, and related documents to ensure compliance with GLP, NIEHS/NTP guidelines, and federal contract requirements.
Review experimental design, methods, and study conduct, with emphasis on rodent toxicology studies.
Verify accuracy and consistency between raw data and final report outputs, and communicate discrepancies through audit reports.
Job description
We are seeking a Quality Assurance (QA) Auditor to support our federal contract with the National Institute of Environmental Health Sciences (NIEHS). The QA Auditor will ensure the accuracy, integrity, and compliance of toxicological research studies, with a focus on rodent models (mice and rats). This position requires strong auditing and QA skills, scientific knowledge of toxicology studies, and proficiency with technology, including modern tools such as AI. The successful candidate will be independent, accountable, and able to deliver polished, GLP-compliant audit reports that meet contract deadlines with minimal oversight, while also collaborating effectively with internal staff and NIEHS stakeholders.
Key Responsibilities- Conduct QA audits of toxicology study reports, laboratory data, pathology tables, electronic records, and related documents to ensure compliance with Good Laboratory Practices (GLP), NIEHS/NTP guidelines, and federal contract requirements.
- Review experimental design, methods, and study conduct, with emphasis on rodent (mice/rat) toxicology studies.
- Verify accuracy and consistency between raw data (e.g., Provantis, CEBS, NELI) and final report outputs.
- Identify, document, and communicate discrepancies through clear audit reports.
- Ensure audit deliverables consistently meet federal timelines, formatting, and technical standards.
- Collaborate with staff/colleagues and government officers/employees to address findings and resolve issues constructively.
- Apply technology and AI tools to enhance auditing efficiency, documentation, and reporting processes.
- Maintain strict attention to confidentiality, accuracy, and data integrity.
- Participate in internal SOP reviews, process improvements, and team training as required.
Required:
- Minimum bachelor's degree in a scientific field (Toxicology, Biology, Chemistry, Environmental Health, or related discipline).
- Demonstrated experience through undergraduate training and/or professional work in Quality Assurance, Regulatory Compliance, and/or Laboratory Research, ideally with a focus on toxicology studies.
- Working knowledge of rodent (mice/rat) study design, conduct, and interpretation.
- Familiarity with Good Laboratory Practices (GLP) and regulatory QA processes.
- Strong proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
- Ability to work effectively on both Windows and Mac operating systems, and troubleshoot basic technology issues independently.
- Basic understanding of AI tools and applications relevant to auditing, data verification, or document review.
- Excellent written and verbal communication skills.
- Strong attention to detail with the ability to work independently, manage multiple audit assignments, and meet deadlines without extensive oversight.
Preferred:
- Experience auditing toxicology reports or laboratory data in a QA role.
- Familiarity with Provantis, CEBS, or NELI data systems.
- Previous experience with federal contracts or regulatory agencies (EPA, FDA, NIEHS, NTP, or OECD).
- Experience utilizing AI tools to support auditing workflows, data analysis, or QA documentation.
- Analytical, detail-oriented, and scientifically grounded.
- Independent and accountable in managing workload and producing audit-ready deliverables.
- Technologically adaptable, with a willingness to learn and apply new digital and AI-based platforms.
- Strong communicator able to collaborate across internal teams and with NIEHS staff.
- Committed to delivering high-quality, GLP-compliant QA products that support NIEHS/NTP's mission in public health.
- U.S. citizenship or permanent resident status required. Must be able to obtain and maintain a National Agency Check (NAC) or equivalent federal background clearance required for access to NIEHS/NTP systems. NIEHS will provide onboarding and security training during system access initiation. No visa sponsorship (e.g., H1-B) is available for this position.
- Employment is contingent upon successful completion of a background check, which may include verification of education, employment history, and references. NIEHS will conduct a National Agency Check prior to granting network and facility access. A drug screening may be required in accordance with company and federal guidelines. NIEHS will provide mandatory onboarding and orientation training upon assignment to the contract.
- NIEHS-issued Mac laptop and secure network credentials will be provided for contract work. Standard office and computer equipment will also be supplied as needed (e.g., monitors, peripherals). The position requires use of Microsoft Office Suite, Adobe Acrobat Professional, and data verification tools such as Provantis, CEBS, or NELI (training provided). No vehicle or specialized physical equipment is required for normal duties.
This position primarily involves computer and desk-based work. The employee should be able to remain in a stationary position for extended periods, operate standard office equipment, and occasionally move about the office to access files or attend meetings. Light lifting of up to 15 pounds may be required. The role requires the ability to focus on detailed tasks, manage multiple priorities, make sound decisions, and communicate effectively. Adaptability, professionalism, and sound judgment are essential. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.
Working Environment- Hybrid environment: combination of remote and on-site work at the NIEHS campus in Research Triangle Park, NC. On-site attendance is occasionally required for meetings, audits, and collaborative activities with NIEHS and CSS team members.
- Minimal travel (<10%) may be required, primarily for training, meetings, or audits conducted at NIEHS or contractor facilities.
At CSS, we are committed to fostering an inclusive and merit-based workplace. We provide equal employment opportunities to all individuals, ensuring that hiring and employment decisions are based on qualifications, skills, and performance. We do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.