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Gmp Auditor Jobs (NOW HIRING)

Aegis Worldwide

Quality Auditor

Indianapolis, IN · On-site

$26.44 - $33.65/hr

Aegis Worldwide Quality Auditor 1st shift/$55-$70k/FULL TIME Indianapolis, IN Overview: Aegis ... Review and release production batches while ensuring compliance with GMP and GLP standards.

Aegis Worldwide

Quality Auditor

Indianapolis, IN · On-site

Aegis Worldwide Quality Auditor 1st shift/$55-$70k/FULL TIME Indianapolis, IN Overview: Aegis ... Review and release production batches while ensuring compliance with GMP and GLP standards.

Merieux NutriSciences

Remote Auditor

Essential Functions and Responsibilities • Conduct audits such as those related to GMP/Food ... The auditor has frequent contact with various clients and suppliers to conduct audits and schedule ...

Grifols

Manager, Quality Audits

Clayton, CA · On-site

This position is part of the global GWWO Auditing Department & entails performing routine GMP audits as well as speciality and technical audits in relation to current products and prospective in ...

GRIFOLS, S.A.

Manager, Quality Audits

Clayton, NC · On-site

This position is part of the global GWWO Auditing Department & entails performing routine GMP audits as well as speciality and technical audits in relation to current products and prospective in ...

Revance

Supplier Quality Auditor

Johnson City, TN

The Supplier Quality Auditor is responsible for executing risk-based GMP audit programs supporting OTC and cosmetic operations. They will ensure compliance with 21 CFR 210/211, ISO 22716, and ...

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How much do gmp auditor jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for gmp 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.

What are the key skills and qualifications needed to thrive in the Gmp Auditor position, and why are they important?

To thrive as a GMP Auditor, you need a thorough understanding of Good Manufacturing Practices, regulatory compliance, and quality assurance, often supported by a degree in life sciences or a related field. Familiarity with industry standards such as ISO guidelines, use of audit management systems, and certifications like Certified Quality Auditor (CQA) are highly beneficial. Strong attention to detail, effective communication, and critical thinking are essential soft skills for this role. These skills ensure accurate assessments, clear reporting, and the ability to work collaboratively with teams to maintain high compliance standards.

What does a typical day look like for a GMP Auditor?

A typical day for a GMP Auditor involves reviewing documentation, conducting on-site inspections, and evaluating manufacturing processes to ensure compliance with regulatory standards. You may spend time preparing audit reports, meeting with quality assurance teams, and providing recommendations for corrective actions. Collaboration with production, laboratory, and regulatory affairs departments is common, and you may be expected to travel between different manufacturing sites. The role is dynamic and requires strong organizational skills to manage multiple audits and deadlines. This position offers a valuable opportunity to contribute to quality assurance and process improvements within the organization.

What is a GMP Auditor job?

A GMP (Good Manufacturing Practices) Auditor is responsible for assessing manufacturing facilities to ensure compliance with regulatory standards and industry best practices. They conduct audits, review documentation, and identify areas for improvement to maintain product safety and quality. GMP Auditors work in industries like pharmaceuticals, biotechnology, and food production, where strict regulations govern production processes. Their role involves reporting findings, recommending corrective actions, and ensuring companies meet legal and ethical standards.

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Gmp Auditor jobs near you
GCP/GMP Auditor - Former FDA / FDA Inspection Experience (Midwest USA)

GCP/GMP Auditor - Former FDA / FDA Inspection Experience (Midwest USA)

SQA Services

Indianapolis, IN • On-site

$4K - $5K/wk

Other

Posted 10 days ago

Job description

For more than 30 years, SQA Services has been a leader in providing managed supplier quality services - including audits, assessments, corrective actions, inspections, remediation, and engineering support - to manufacturers across regulated industries. We deploy experienced auditors across the United States and in over 90 countries to support client and supplier sites on demand.
 

SQA Services is seeking a senior auditor with former FDA experience and direct FDA inspection exposure to support a 4-day mock FDA Pre-Approval Inspection (PAI) in Indianapolis, Indiana.

This engagement will simulate an FDA inspection environment, requiring an auditor who understands FDA expectations, inspection readiness, and compliance risks across GCP and GMP operations. The auditor will play a key role in assessing readiness and identifying gaps prior to a regulatory inspection.

Auditors located in the Midwest U.S. or willing to travel are preferred.

Key Responsibilities
  • Conduct a mock FDA Pre-Approval Inspection (PAI) in alignment with FDA expectations
  • Evaluate compliance to Good Clinical Practices (GCP) and 21 CFR 210/211 (GMP)
  • Assess inspection readiness, quality systems, and documentation practices
  • Identify compliance gaps and potential regulatory risks
  • Provide detailed audit findings and recommendations
  • Prepare and deliver audit reports per client and SQA standards
  • Communicate observations clearly to stakeholders and leadership
Required Qualifications
  • Direct experience supporting/hosting FDA inspections
  • Experience conducting mock FDA inspections or PAI readiness assessments
  • Strong experience auditing to GCP and 21 CFR 210/211 (GMP)
  • Proven ability to conduct regulatory-style audits (PAI readiness or mock FDA inspections)
  • Strong understanding of FDA inspection processes and expectations
  • Excellent reporting, communication, and stakeholder engagement skills
  • Willingness to travel to Indianapolis, IN for a 4-day audit
Preferred Qualifications
  • Background in clinical and commercial pharmaceutical environments
  • Experience supporting high-visibility or regulatory-critical audits
  • Located in the Midwest U.S.
$4,500 - $5,000 a week
4-day audit Pay Rate inclusive of preparation, travel, audit execution, reporting, and follow-up.
Travel expenses reimbursed at cost with receipts per SQA travel policy.
 
Note:
 
SQA is an Equal Opportunity Employer. Employment is based on merit and qualifications, and is not influenced by race, color, religion, gender, national origin, veteran status, disability, age, sexual orientation, gender identity, marital status, or any other legally protected status.
 
This position requires access to ITAR-controlled technical data and/or defense articles. As such, the candidate must be a U.S. citizen or U.S. lawful permanent resident (green card holder) to comply with the International Traffic in Arms Regulations (ITAR). Applicants who do not meet these criteria will not be considered for this role.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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