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Glp Auditor Jobs (NOW HIRING)

Pharmatech Associates

$125 - $150/hr

Pharmatech Associates is seeking an experienced GLP Auditor, Contract/Project Consultant to support upcoming audits for our clients conducting regulated nonclinical research and animal studies ...

Labcorp

Lead Internal Auditor, GLP/GCP

Indianapolis, IN · On-site

Labcorp is seeking a Lead Internal Auditor, GLP/GCP to join our team in Indianapolis, IN ! Work Schedule: Monday Through Friday 8-5 pm Job Responsibilities: The Lead Internal Auditor plays a pivotal ...

Labcorp

Lead Internal Auditor, GLP/GCP

Indianapolis, IN · On-site

Labcorp is seeking a Lead Internal Auditor, GLP/GCP to join our team in Indianapolis, IN ! Work Schedule: Monday Through Friday 8-5 pm Job Responsibilities: The Lead Internal Auditor plays a pivotal ...

Labcorp

Quality Auditor - GLP/GCP

Indianapolis, IN · On-site

Labcorp is seeking a Quality Auditor, GLP/GCP to join our team in Indianapolis, IN Work Schedule: Monday Through Friday 8-5 pm Job Responsibilities: The Quality Auditor plays a pivotal role as part ...

Labcorp

Quality Auditor - GLP/GCP

Indianapolis, IN

Labcorp is seeking a Quality Auditor, GLP/GCP to join our team in Indianapolis, IN Work Schedule: Monday Through Friday 8-5 pm Job Responsibilities: The Quality Auditor plays a pivotal role as part ...

Altasciences

Senior QA Auditor

Everett, WA · On-site

$80K - $87K/yr

Audits all disciplines (examples of disciplines include Method Validations, Non- Clinical GLP ... Acts as lead auditor on studies and projects. * Maintains computerized files to support audit ...

Scorpion Therapeutics

Lead Supplier Auditor

Pasadena, CA · On-site

$150 - $200/hr

Prior GMP/GLP/GCP/GVP auditing, training, and/or compliance investigation experience * CSV and data integrity audit knowledge beneficial * Travel to other Arrowhead locations and domestic ...

Vaxcyte

Manager, Supplier & Internal Auditor

San Carlos, CA · On-site +1

$151K - $176K/yr

The ideal candidate is a certified auditor with strong working knowledge of GMP, GLP, GCP, ICH, and ISO 13485 requirements and experience auditing within the pharmaceutical, biotechnology, or medical ...

Sotera Health

Quality Auditor I or II

Nelson, NE · On-site

Review GLP studies for completeness, accuracy, compliance, and concurrence. * Audit studies ... Quality Auditor II * 2+ years of laboratory, quality assurance, or auditing experience in a ...

CSS Inc

Quality Assurance (QA) Auditor

Durham, NC · On-site

$100 - $125/hr

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 ...

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Glp Auditor information

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How much do glp auditor jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for glp auditor in the United States is $19.21, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

What is a GLP auditor?

GLP Auditors are professionals responsible for ensuring that laboratories and research facilities comply with Good Laboratory Practice (GLP) regulations. They conduct audits, inspections, and reviews of laboratory processes, documentation, and data to verify compliance with national and international GLP standards. Their work helps ensure the integrity, reliability, and quality of non-clinical laboratory studies, which are often required for regulatory submissions. GLP Auditors may work internally within organizations or as external consultants, and their findings can lead to corrective actions or improvements in laboratory practices.

What are the key skills and qualifications needed to thrive as a GLP auditor?

To thrive as a GLP Auditor, you need in-depth knowledge of Good Laboratory Practice standards, regulatory compliance, and quality assurance principles, often backed by a degree in life sciences or a related field. Proficiency with audit management software, document control systems, and relevant certifications such as RQA or ASQ are typically required. Strong analytical thinking, attention to detail, and effective communication skills help auditors identify compliance gaps and interact with laboratory staff. These skills are crucial for ensuring laboratories meet regulatory standards, maintain data integrity, and avoid costly non-compliance issues.

What are some typical challenges faced by a GLP auditor during inspections, and how are they addressed?

GLP Auditors often encounter challenges such as navigating complex documentation, ensuring compliance across diverse departments, and addressing discrepancies in data integrity. These challenges are managed by maintaining up-to-date knowledge of GLP regulations, developing strong communication skills to facilitate clear discussions with laboratory staff, and employing systematic auditing techniques to thoroughly review records. Effective GLP Auditors also foster collaborative relationships with teams to encourage a culture of continuous improvement and compliance.

What is the difference between Glp Auditor vs Quality Assurance Auditor?

AspectGlp AuditorQuality Assurance Auditor
CertificationsGxP, GLP, ISOISO, GMP, GxP
Work EnvironmentPharmaceutical, biotech labs, clinical researchManufacturing, production, labs
Industry UsageRegulated clinical and preclinical studiesProduct quality, manufacturing compliance

Both roles focus on ensuring compliance with industry standards, but Glp Auditors specialize in Good Laboratory Practice regulations for clinical and preclinical research, while Quality Assurance Auditors oversee broader quality systems across manufacturing and production environments. Understanding these differences helps professionals target their skills and certifications effectively.

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For Glp Auditor jobs, the most frequently searched job titles are:

Glp Auditor jobs near you
Infographic showing various Glp Auditor job openings in the United States as of September 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 100% In-person job distribution, with an average salary of $39,947 per year, or $19.2 per hour.

GLP Auditor, Part 58, Animal Studies

Raleigh, NC • On-site

Pharmatech Associates
1 - 10 employees
Learn more about Pharmatech Associatesexternal

$100 - $125/hr

Other

Posted 9 days ago

Job description

Pharmatech is proud to be an equal opportunity employer. Together we are committed to fostering an environment that is professional, inclusive and diverse. Explore the exciting opportunities currently available in the US and around the world.

Pharmatech Associates is seeking an experienced GLP Auditor, Contract/Project Consultant to support upcoming audits for our clients conducting regulated nonclinical research and animal studies

Position Overview

The GLP Auditor will provide independent assessment of contract GLP laboratories and their associated work as part of supplier oversight processes. The role requires the ability to assess not only whether procedures are followed, but also whether the resulting data can be relied upon, reconstructed, and supported by appropriate documentation. The successful candidate will be comfortable working directly with animal study records, laboratory data, protocols, raw data, computerized systems, equipment, facilities, and final reports, while applying the requirements of 21 CFR Part 58 and applicable regulatory expectations.

Key Responsibilities
  • Assess compliance with 21 CFR Part 58 principles, study protocols, SOPs, and applicable regulatory requirements.
  • Assess the effectiveness of the facilities QAU including study oversight.
  • Assess the adequacy of controls surrounding analytical methods, method validation, laboratory procedures, system suitability, and test results, as applicable.
  • Examine the qualification, calibration, maintenance, and operational status of laboratory and study equipment.
  • Evaluate computerized systems and electronic data environments, including validation status, user access, audit trails, data controls, and record retention.
  • Assess animal research environments, including animal identification, housing, care, environmental controls, facility practices, and associated documentation.
  • Prepare audit agendas and comprehensive audit reports that clearly distinguish regulatory findings, quality risks, supporting evidence, and potential impact on study integrity.
  • Review proposed remediation and CAPA plans, assess root-cause considerations, and verify that corrective actions are appropriately implemented and effective.
  • Provide practical recommendations regarding SOPs, processes, training, documentation practices, and quality controls where improvements are needed.
  • May be required to perform study audits as part of our client’s non-clinical study oversight.
Required Qualifications
  • At least 5 years of experience in GLP Quality Assurance, nonclinical research, or regulated auditing.
  • Must be able to travel to perform audits.
  • Demonstrated working knowledge of 21 CFR Part 58 requirements.
  • Direct experience auditing nonclinical facilities and studies to support pharmaceutical or biopharmaceutical product development.
  • Experience performing study audits, critical-phase audits, facility assessments, and/or external partner audits.
  • Ability to independently assess study documentation, raw data, source records, protocols, deviations, and final reports.
  • Understanding of data integrity principles, including ALCOA+ expectations, and their practical application to GLP records.
  • Strong technical writing skills and the ability to communicate audit conclusions clearly and objectively.

Pharmatech Associates, Inc. provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law.

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