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Glp Consulting Jobs (NOW HIRING)

Salesforce, Inc.

Licensing Consultant

Indianapolis, IN · On-site

As a Licensing Consultant on the Global Licensing Programs (GLP) team, you serve as a critical strategic advisor and escalation point within the Salesforce Foundations ecosystem-spanning Tableau, CRM ...

Salesforce, Inc.

Licensing Consultant

Indianapolis, IN · On-site

$110 - $160/hr

As a Licensing Consultant on the Global Licensing Programs (GLP) team, you serve as a critical strategic advisor and escalation point within the Salesforce Foundations ecosystem--spanning Tableau, CR ...

Aquinas Consulting

Scientist II-IV

Ridgefield, CT

Aquinas Consulting is currently looking to fill a Scientist II job focused on pharmaceutical ... GMP, GLP, and other regulatory standards · Contribute to method development, validation, and ...

IV Drips

Nurse Practitioner

Brooklyn, NY · Remote

$200 - $800/day

What You'll Do As part of our GLP-1 care team, you'll: * Conduct virtual consultations (15-30 minutes) to assess eligibility and prescribe treatment * Review patient histories and labs as needed

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Glp Consulting information

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$5

$47

$62

How much do glp consulting jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for glp consulting in the United States is $47.06, according to ZipRecruiter salary data. Most workers in this role earn between $39.18 and $52.88 per hour, depending on experience, location, and employer.

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

To thrive as a GLP Consultant, you need in-depth knowledge of Good Laboratory Practice regulations, scientific expertise (often with a degree in life sciences), and experience in laboratory environments. Familiarity with regulatory guidelines, auditing tools, quality management systems, and relevant certifications like RQAP-GLP are typically required. Strong analytical thinking, attention to detail, and effective communication skills help consultants navigate compliance issues and provide actionable recommendations. These skills ensure laboratories meet compliance standards, avoid regulatory penalties, and maintain high-quality research practices.

What are some common challenges faced by GLP consultants when ensuring compliance for clients in the life sciences industry?

GLP consultants often encounter challenges such as interpreting evolving regulatory requirements, managing complex documentation, and ensuring that client laboratories implement consistent quality practices. They must stay updated on both local and international GLP standards and tailor their advice to meet the specific needs of each client. Additionally, consultants frequently navigate resistance to change within organizations and work closely with multidisciplinary teams to foster a culture of compliance.

What is GLP consulting?

GLP consulting refers to professional advisory services that help organizations comply with Good Laboratory Practice (GLP) regulations. These consultants provide expertise on setting up, maintaining, and auditing laboratory systems to ensure data integrity, quality, and regulatory compliance, often for organizations involved in research, pharmaceuticals, or chemicals. GLP consultants can support staff training, documentation, facility design, and process optimization to meet regulatory standards required by agencies like the FDA or EMA.

What is the difference between Glp Consulting vs Regulatory Affairs Specialist?

AspectGlp ConsultingRegulatory Affairs Specialist
Required CredentialsBachelor's degree, industry certificationsBachelor's degree, certifications like RAC often preferred
Work EnvironmentConsulting firms, client sites, officesPharmaceutical, biotech, or healthcare companies
Employer & Industry UsageConsulting firms across various industriesPharmaceutical, biotech, healthcare sectors
Common Search & ComparisonYesYes

While both roles require a background in life sciences and industry certifications, Glp Consulting typically involves providing expert advice across multiple clients and industries, whereas a Regulatory Affairs Specialist focuses on ensuring compliance within a specific company or product line in the pharmaceutical or biotech sectors.

More about Glp Consulting jobs
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Glp Consulting jobs near you
Infographic showing various Glp Consulting job openings in the United States as of August 2026, with employment types broken down into 72% Full Time, 14% Part Time, and 14% Contract. Highlights an 85% In-person, 5% Hybrid, and 10% Remote job distribution, with an average salary of $97,888 per year, or $47.1 per hour.

Director, GLP Quality Assurance

Revolution Medicines

Redwood City, CA • Hybrid

Full-time

Re-posted 8 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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