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Gxp Auditor Jobs (NOW HIRING)

Communicate audit results, CAPAs, and GxP guidance to Quality and Business teams to drive quality ... Oversee contract auditors and others performing audits on Arrowhead's behalf * Maintain vendor/site ...

The Senior Manager, GxP Computerized Systems Auditing, is responsible for managing and executing a risk-based audit program for computerized systems used in GxP-regulated environments. This role ...

Role OverviewThe Associate Director, GxP Compliance and Auditing, serves as the strategic leader for the development, implementation, and continuous enhancement of Legend Biotech's global GxP ...

Supports inspection readiness activities as a co-auditor. * Participates in mock inspections with ... Maintain current knowledge of applicable GxP regulations and industry best practices. * Support ...

Supports inspection readiness activities as a co-auditor. * Participates in mock inspections with ... Maintain current knowledge of applicable GxP regulations and industry best practices. * Support ...

The Quality Assurance Auditor III leads complex and/or multi‑department internal and/or external ... Provide GxP consultation and support to project teams and external clients. * Lead process audits ...

Night Auditor / Front Desk Agent The Westin Westminster Job Summary The Westin Westminster is ... Utilize GXP to document guest requests and follow up to ensure completion. * Provide information ...

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How much do gxp auditor jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for gxp 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.
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Infographic showing various Gxp Auditor job openings in the United States as of August 2026, with employment types broken down into 85% Full Time, 10% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 89% Physical, 5% Hybrid, and 6% Remote job distribution, with an average salary of $39,947 per year, or $19.2 per hour.

Clinical Quality Auditor

South San Francisco, CA • On-site

Astrix Inc
Recruiting and Staffing Services • 1 - 5K employees

$60 - $75/hr

Full-time, Contractor

This job post has expired 3 days ago. Applications are no longer accepted.


Job description

Our client is a patient-driven cardiovascular biotechnology company dedicated to advancing heart disease treatment by developing therapies that address the root causes of disease rather than managing symptoms alone.
Title: GCP Auditor
Location: Hybrid (3 days onsite, South San Francisco, CA)
Pay rate: $60-75hr+ Depends on experience
Schedule: Full-time, M-F 8am-5pm
Contract-to-hire
We are seeking a GxP Auditor to join a quality team in a contract-to-hire capacity. This role is ideal for a seasoned auditor with strong GMP experience who is looking to contribute to a growing organization while supporting and helping scale a global audit program.
Role Overview
The GxP Auditor will be responsible for executing and supporting audits across internal operations, vendors, and investigator sites, ensuring compliance with global regulatory standards. This individual will also play a key role in strengthening audit program infrastructure, supporting audit reporting, and managing CAPA lifecycle activities.
Key Responsibilities
  • Plan and conduct GxP audits (primarily GMP), including vendor and clinical/investigator site audits
  • Perform audit report reviews and ensure alignment with regulatory and quality standards
  • Support the audit lifecycle, including CAPA review, approval, and closure
  • Contribute to the development and improvement of audit program infrastructure
  • Collaborate cross-functionally with Quality and Operations teams
  • Participate in scheduled audits across multiple regions (domestic and some international travel)
  • Support upcoming GCP audits and ongoing audit planning activities
  • Travel: 20-50%

Qualifications
  • MUST be a Certified Auditor (required)
  • 5-10+ years of experience in Quality, Compliance, or GxP auditing/inspections
  • Strong working knowledge of FDA, EMA, ICH, and GMDP regulations
  • Hands-on experience conducting GMP audits (vendor and/or clinical site audits preferred)
  • Experience reviewing audit reports and managing CAPAs
  • Bachelor's or advanced degree in Life Sciences, Pharmacy, Chemistry, or related field
  • Experience in biotech/pharma environments
Preferred
  • Experience with MHRA and Health Canada regulations
  • Familiarity with Veeva and/or Smartsheets
  • Strong communication, collaboration, and stakeholder management skills

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