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Glp Qa Jobs (NOW HIRING)

Legend Biotech US

Sr. Manager, CQA GLP

Somerset, NJ · Hybrid

Support the GLP quality compliance systems, via established policies and procedures for the GLP QA function. * Manage GLP quality systems including the implementation and maintenance of procedures ...

Jade Biosciences

The ideal candidate brings hands-on expertise in GCP, GPvP and GLP QA operations, a proactive approach to problem-solving, and the ability to guide and influence cross-functional teams while ...

Smithers

Quality Assurance Specialist

Wareham, MA · On-site

$25 - $28.85/hr

Maintain confidentiality and independence in all QA activities and assessments GLP Accountability The Quality Assurance Specialist is accountable for supporting the organization's GLP Quality ...

Exelixis

Senior GCP/PV/GLP QA Manager

Alameda, CA · On-site

$163K - $231K/yr

The Senior GCP/GVP QA Manager is accountable for assisting with the development, implementation and maintenance of end-to-end QA systems and activities for GCP/GLP operations, including planning and ...

Exelixis

Associate GCP/GLP QA Director

Alameda, CA

$177K - $251K/yr

This key role drives consistency across QA systems and processes for the Clinical QA team, identifying issues and risks, escalating in a timely fashion, and aligning metrics that provide input into a ...

Exelixis

Senior GCP/PV/GLP QA Manager

Alameda, CA

$163K - $231K/yr

The Senior GCP/GVP QA Manager is accountable for assisting with the development, implementation and maintenance of end-to-end QA systems and activities for GCP/GLP operations, including planning and ...

Exelixis

Associate GCP/GLP QA Director

Alameda, CA · On-site

$177K - $251K/yr

This key role drives consistency across QA systems and processes for the Clinical QA team, identifying issues and risks, escalating in a timely fashion, and aligning metrics that provide input into a ...

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How much do glp qa jobs pay per year?

As of Jul 17, 2026, the average yearly pay for glp qa in the United States is $118,074.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $144,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Glp Qa position, and why are they important?

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 is a GLP QA job?

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 are the typical responsibilities of a GLP QA professional on a day-to-day basis?

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.

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Glp Qa jobs near you
Infographic showing various Glp Qa job openings in the United States as of July 2026, with employment types broken down into 89% Full Time, 2% Temporary, and 9% Contract. Highlights an 91% In-person, 2% Hybrid, and 7% Remote job distribution, with an average salary of $118,074 per year, or $56.8 per hour.
Director, GLP Quality Assurance

Director, GLP Quality Assurance

Revolution Medicines

Redwood City, CA • Hybrid

Other

Re-posted 16 days ago

Job description

The Opportunity:

  • The Director, Good Laboratory Practice Quality Assurance (GLP QA) is responsible for ensuring Good Laboratory Practices (GLP) compliance at RevMed and external vendors contracted to perform regulated work on behalf of RevMed including all GLP vendors.

  • Responsibilities include research laboratory vendors that perform work to support regulated clinical studies.

  • Develops the annual vendor audit plan.

  • The Director GLP QA performs and/or manages vendor audits including:

    • Development of the audit plan, audit conduct, and reporting

    • Tracking and coordination of audit closure tasks including review of observation responses from vendor(s) in conjunction with operational subject matter experts (SMEs), as applicable.

    • Provision of vendor approval recommendations

    • Maintenance of vendor approval status in Veeva.

    • Development and/or review of Quality Agreements

  • Performs or participates in internal audits.

  • Provides QA review of CRO study protocols and reports for compliance utilizing a risk-based approach, as needed and serves as an advisor to the Nonclinical Development and Clinical Pharmacology (NDCP) to resolve compliance issues.

  • Monitors vendor QA units for compliance with applicable regulations including review of vendor study specific QA audit reports.

  • Advises Sponsor(s) on compliance requirements for test and control article used in GLP studies.

  • Liaises and/or consults with GLP vendor QA departments on study-related issues such as deviations, investigations, CAPAs and other compliance issues.

  • Provides annual GLP training or liaises with an external trainer to provide GLP training to RevMed functional team(s).

  • Attends functional area meetings (e.g., NDCP and Biomarker group) to discuss and review new or on-going issues, projects, and/or studies.

  • Works with QA management for resource planning, as needed.

  • Attends periodic clinical QA group meetings, as needed.

  • Provides periodic quality and compliance updates to QA management.

  • Develops/prepares standard operating procedure (SOPs) content to GLP audits, and reviews functional area and QA SOPs for GLP compliance.

  • Provides consultative QA guidance for computerized system vendors (and systems) supporting GLP studies.

Required Skills, Experience and Education:

  • Bachelor's or Master's Degree.

  • 12+ years of experience in global Good Laboratory Practice (GLP) Quality Assurance (QA).

  • Extensive audit and inspection management experience.

Preferred Skills:

  • Registered Quality Assurance Professional - Good Laboratory Practice (RQAP-GLP).

  • Planning and scheduling expertise.

  • Experienced in effective prioritization of competing initiatives and tasks across multiple projects.

  • Ability to communicate effecttively with senior leadership, management and cross functional teams.

  • Ability to manage workstreams to maintain delivery timelines through disciplined planning, tracking and follow-up.

  • Ability to balance detail-oriented execution with strategic oversight.

  • Experienced with the proactive identification, assessment and mitigation of risks and with timely issue escalation, as applicable.

  • Regulatory expertise with at least the following regulations and guidance:

    • 21CFR Part 58 Good Laboratory Practice.

    • 21 CFR Part 11 Electronic Records; Electronic Signatures.

    • OECD #1 - 24 Standards and Advisory Documents on Good Laboratory Practices.

    • ICH E6 (R2 and R3) Good Clinical Practices.

    • Japanese Ministry of Health Labor and Welfare (MHLW) - Good Laboratory Practice.

    • Applicable US and EU guidance documents including bioanalytical, in vitro and in vivo genetic, Phototox, and hERG toxicology studies.

  • Experience with the following audit types

  • Testing facilities.

  • Bioanalytical and PK data analysis Labs.

  • hERG and Phototoxicity testing facilities.

  • Archives - biorepositories, paper and electronic data storage.

  • Computer Systems Validation.

  • Biomarker Labs (including Artificial Intelligence and Machine Learning).

  • Central Laboratories. 

    #LI-Hybrid #LI-JC1

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