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Vp Glp Qa Jobs (NOW HIRING)

Celldex Therapeutics

GLP QA Specialist II

Fall River, MA · On-site

$76K - $99K/yr

Overview This role is responsible for maintaining quality systems, tracking and reporting QA metrics, managing laboratory documentation processes, and ensuring adherence to FDA GLP requirements while ...

Frontage Laboratories

QA Specialist-GLP/BIO

Exton, PA · On-site

Quality Assurance Specialist Bio-Analytical GLP Location: Exton PA Reports to : Director BIO GLP Quality assurance Full-time Position/Job Summary: Are you ready for a role that will combine your ...

Russell Solutions Group

VP RA/QA

Mountain View, CA · On-site

... quality assurance functions. This person will drive the global regulatory affairs strategy, leading the execution of regulatory filings and managing any applicable personnel. The VP of Regulatory ...

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Vp Glp Qa information

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How much do vp glp qa jobs pay per year?

As of Sep 4, 2026, the average yearly pay for vp glp qa in the United States is $157,532.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,000.00 and $190,000.00 per year, depending on experience, location, and employer.

What are the responsibilities of a VP GLP QA?

A VP GLP QA (Vice President of Good Laboratory Practice Quality Assurance) oversees the quality assurance programs for non-clinical laboratory studies to ensure compliance with GLP regulations. Their responsibilities include developing and maintaining QA systems, leading audits and inspections, providing training on regulatory standards, and ensuring that all data and processes meet both company and regulatory requirements. They work closely with other departments to identify and mitigate risks, manage QA teams, and serve as the primary contact for regulatory agencies during inspections or audits.

What are some common challenges faced by a VP GLP QA, and how can they be effectively addressed?

A VP of GLP QA often encounters challenges such as ensuring consistent compliance with evolving Good Laboratory Practice (GLP) regulations across multiple sites and teams, managing cross-functional communication, and overseeing complex audits. Addressing these challenges requires establishing robust quality systems, continuous training programs, and fostering a culture of transparency and accountability. Regularly collaborating with regulatory affairs, laboratory staff, and executive leadership ensures alignment on quality priorities and swift resolution of compliance issues.

What are the key skills and qualifications needed to thrive as a VP GLP QA, and why are they important?

To thrive as a VP GLP QA (Vice President of Good Laboratory Practice Quality Assurance), you need deep expertise in GLP regulations, quality management systems, and extensive experience in laboratory operations, typically backed by an advanced science degree. Familiarity with audit management software, regulatory databases, and industry certifications such as ASQ Certified Quality Auditor are highly valuable. Exceptional leadership, strategic thinking, and strong communication skills set top performers apart in this role. These skills are crucial for ensuring regulatory compliance, maintaining high-quality standards, and effectively leading cross-functional teams in a regulated laboratory environment.

What is the difference between Vp Glp Qa vs Quality Assurance Manager?

AspectVp Glp QaQuality Assurance Manager
CertificationsGxP, GLP, QA certificationsISO, Six Sigma, QA certifications
Work EnvironmentPharmaceutical, biotech labs, regulated industriesManufacturing, software, healthcare sectors
ResponsibilitiesOversees GLP compliance, validation, auditsManages QA processes, audits, process improvements

The Vp Glp Qa focuses on GLP compliance and validation in regulated industries like pharmaceuticals, while the Quality Assurance Manager oversees broader QA processes across various sectors. Both roles require similar certifications but differ in scope and industry focus.

What cities are hiring for Vp Glp Qa jobs?

Cities with the most Vp 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 Vp Glp Qa jobs?

States with the most job openings for Vp Glp Qa jobs include:

Vp Glp Qa jobs near you
Infographic showing various Vp Glp Qa job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 3% Part Time, 7% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $157,532 per year, or $75.7 per hour.

Director, GLP Quality Assurance

Revolution Medicines

Redwood City, CA • Hybrid

Full-time

Re-posted 4 days ago

Key responsibilities

  • Develops and manages vendor audit plans, conducts audits, and reports on GLP compliance.

  • Reviews and provides guidance on GLP study protocols, reports, and vendor QA reports to ensure regulatory compliance.

  • Provides GLP training, develops SOPs related to GLP audits, and advises on compliance issues related to GLP studies.

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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