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Live In Glp Qa Jobs (NOW HIRING)

Legend Biotech US

Sr. Manager, CQA GLP

Somerset, NJ · Hybrid

She/he may be involved in overseeing the work performed by external contract research organizations ... Support the GLP quality compliance systems, via established policies and procedures for the GLP QA ...

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

... end QA systems and activities for GCP/GLP operations, including planning and supporting vendor ... Assists in the management of Exelixis partnerships and collaborations and forges strong ...

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 ... Participates in identifying and implementing process and system improvements Supervisory ...

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 ... Participates in identifying and implementing process and system improvements Supervisory ...

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Live In Glp Qa information

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How much do live in glp qa jobs pay per year?

As of Jul 18, 2026, the average yearly pay for live in 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 is the difference between Live In Glp Qa vs Live In Glp Auditor?

AspectLive In Glp QaLive In Glp Auditor
CertificationsGMP, GLP knowledge, QA certificationsGMP, GLP, QA certifications
Work EnvironmentPharmaceutical or biotech labs, manufacturing facilitiesPharmaceutical or biotech labs, manufacturing facilities
Employer & IndustryPharma companies, contract research organizationsPharma companies, contract research organizations
Primary FocusEnsuring GLP compliance in QA processesAuditing GLP compliance and documentation

Both Live In Glp Qa and Live In Glp Auditor roles involve ensuring GLP compliance within pharmaceutical environments. The main difference is that Live In Glp Qa focuses on quality assurance activities, while Live In Glp Auditor emphasizes conducting audits and assessments. Both positions require similar certifications and work in comparable environments, but their core responsibilities differ slightly.

What cities are hiring for Live In Glp Qa jobs? Cities with the most Live In Glp Qa job openings:
What are the most commonly searched types of Glp Qa jobs? The most popular types of Glp Qa jobs are:
Live In Glp Qa jobs near you
Director, GLP Quality Assurance

Director, GLP Quality Assurance

Revolution Medicines

Redwood City, CA • Hybrid

Other

Re-posted 17 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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