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Fda Auditor Jobs in California (NOW HIRING)

This includes, but is not limited to, the Food and Drug Administration (FDA) in the United States ... Also, the role will be responsible for all aspects of auditing to ensure regulation compliance ...

This includes, but is not limited to, the Food and Drug Administration (FDA) in the United States ... Also, the role will be responsible for all aspects of auditing to ensure regulation compliance ...

This includes, but is not limited to, the Food and Drug Administration (FDA) in the United States ... Also, the role will be responsible for all aspects of auditing to ensure regulation compliance ...

This includes, but is not limited to, the Food and Drug Administration (FDA) in the United States ... Also, the role will be responsible for all aspects of auditing to ensure regulation compliance ...

Senior GCP Auditor

Culver City, CA · On-site

$88K - $108K/yr

Designated an FDA Breakthrough Therapy, ANKTIVA is the first FDA-approved immunotherapy for non ... Position Summary The Senior GCP Auditor ensures GCP compliance with ImmunityBio entity standard ...

FDA Senior Analyst

Los Angeles, CA · On-site +1

$105K - $120K/yr

... auditors. If you're looking to build highly marketable skills and make a visible impact in a growing organization, this role provides an exceptional platform for career growth. This is a hybrid ...

FDA Senior Analyst

Los Angeles, CA · Hybrid

$105K - $120K/yr

... auditors. If you're looking to build highly marketable skills and make a visible impact in a growing organization, this role provides an exceptional platform for career growth. This is a hybrid ...

Ensure suppliers meet ISO 13485 and FDA QSR/QMSR expectations. Supplier Auditing and Oversight * Plan and execute supplier audits in accordance with risk-based audit schedules. * Evaluate compliance ...

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

Manage the Internal Audit program, including audit scheduling, auditor assignments, and audit ... Solid knowledge of FDA regulations and interpretation of FDA regulations, guidelines and policy ...

Quality Systems Manager

Irvine, CA · On-site

$100 - $145/hr

Manage the Internal Audit program, including audit scheduling, auditor assignments, and audit ... Solid knowledge of FDA regulations and interpretation of FDA regulations, guidelines and policy ...

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Showing results 1-20

Fda Auditor information

See California salary details

$32.6K

$75.3K

$119.9K

How much do fda auditor jobs pay per year?

As of Aug 30, 2026, the average yearly pay for fda auditor in California is $75,257.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,800.00 and $97,200.00 per year, depending on experience, location, and employer.

What is an FDA auditor?

An FDA Auditor is responsible for inspecting facilities, processes, and documentation to ensure compliance with U.S. Food and Drug Administration (FDA) regulations. They review manufacturing practices, quality control systems, and regulatory filings for industries such as pharmaceuticals, medical devices, and food production. FDA Auditors may work for the FDA or for companies preparing for FDA inspections. Their role helps ensure public safety by verifying that products meet legal and quality standards.

What are the key skills and qualifications needed to thrive as an FDA auditor?

To thrive as an FDA Auditor, you need a strong background in life sciences, regulatory compliance, and audit methodologies, usually supported by a relevant degree and professional certifications such as RAC or CQA. Familiarity with FDA regulations (such as 21 CFR), electronic quality management systems (eQMS), and audit management tools is essential. Attention to detail, critical thinking, and strong communication skills help auditors navigate complex regulatory settings and interact effectively with stakeholders. These competencies are crucial for ensuring companies meet rigorous FDA standards and maintain regulatory compliance.

What are the primary challenges FDA auditors face during compliance inspections?

FDA Auditors often encounter challenges such as interpreting complex and evolving regulatory guidelines, managing on-site audits in diverse environments, and reviewing extensive documentation under tight timeframes. They must adapt quickly to various industry settings, handle potentially uncooperative stakeholders, and maintain objectivity throughout their evaluations. Successfully overcoming these challenges requires resilience, up-to-date regulatory knowledge, and excellent people skills. These hurdles are a vital part of ensuring public health and safety by holding organizations to the highest standards of compliance.

How to become an FDA auditor?

To become an FDA auditor, candidates typically need a bachelor's degree in a relevant field such as life sciences, chemistry, or pharmacy, along with experience in quality assurance or regulatory compliance. Professional certifications like Certified Quality Auditor (CQA) or training in Good Manufacturing Practices (GMP) are often required or preferred. Strong attention to detail, knowledge of FDA regulations, and auditing skills are essential for success in this role.

What do FDA auditors make?

FDA auditors typically earn a salary that ranges from $60,000 to $100,000 annually, depending on experience, location, and employer. They may also receive benefits such as health insurance, paid time off, and sometimes overtime pay, especially when conducting inspections or audits outside regular hours.

What are the most commonly searched types of Fda Auditor jobs in California?

The most popular types of Fda Auditor jobs in California are:

What cities in California are hiring for Fda Auditor jobs?

Cities in California with the most Fda Auditor job openings:

Infographic showing various Fda Auditor job openings in California as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 2% Contract, and 1% Nights. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $75,257 per year, or $36.2 per hour.

Clinical Quality Auditor

Astrix Inc

South San Francisco, CA • On-site

$60 - $75/hr

Full-time, Contractor

Re-posted 14 days ago


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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