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Gmp Auditor Jobs (NOW HIRING)

Global Placement Firm

Sr. Auditor

Paramus, NJ · On-site

$69 - $110/hr

Sr. Auditor Quality Assurance (Pharmaceuticals) Location: Paramus, NJ (100% On-Site) - 5 month ... Assess compliance with FDA, EMA, ICH, and international GMP/GDP regulations . * Review and evaluate ...

Global Placement Firm

Sr. Auditor

Paramus, NJ

$67/hr

Sr. Auditor Quality Assurance (Pharmaceuticals) Location: Paramus, NJ (100% On-Site) - 5 month ... Assess compliance with FDA, EMA, ICH, and international GMP/GDP regulations . * Review and evaluate ...

TechData Service Company LLC

Be Seen First

Manager, Quality Auditing (Contractor)-LC00002

Exton, PA · On-site

$45.80 - $49.80/hr

This is a high-impact, independent role requiring deep GMP expertise, strong auditing experience, and the ability to influence stakeholders across a global network. The contractor will conduct ...

DQS

Contract Medical Device Lead Auditor

Schaumburg, IL · On-site

Experience with internal, 2nd or 3rd party ISO-9001, ISO 13485, and/ or GMP auditing. * Preference given to RAB-QSA or Exemplar Global Lead Auditor or Auditor qualification. * Ability to develop an ...

Fortis Construction

GMP Accountant

Portland, OR

This role performs many vital accounting responsibilities and is responsible for the auditing ... A successful GMP Accountant is detail oriented with good problem-solving skills and the ability to ...

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 ...

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How much do gmp auditor jobs pay per hour?

As of Aug 19, 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 is a GMP auditor?

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.

What does a GMP auditor do?

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 are the key skills and qualifications needed to thrive as a GMP auditor?

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.

How do you become a GMP auditor?

To become a GMP auditor, individuals typically need a background in life sciences, pharmacy, or related fields, along with experience in pharmaceutical or manufacturing environments. Certification from recognized organizations, such as the American Society for Quality (ASQ) or equivalent, is often required, and auditors should develop knowledge of Good Manufacturing Practices and auditing techniques. Gaining experience through training programs and understanding regulatory requirements is essential for this role.
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Gmp Auditor jobs near you
Infographic showing various Gmp Auditor job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, 25% Temporary, and 25% Contract. Highlights an 100% In-person job distribution, with an average salary of $39,947 per year, or $19.2 per hour.

Senior Pharmaceutical Quality Auditor (GMP / Medical Device)

SQA Services, Inc.

Anaheim, CA • On-site

$221.40 - $258.30/hr

Other

Posted yesterday

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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 and quality professionals across the United States and in over 90 countries to support client and supplier sites on demand.

SQA Services is seeking a Senior Pharmaceutical Quality Auditor to support ongoing supplier audits throughout Southern California and surrounding regions.

This role requires a highly experienced auditor with a strong background in pharmaceutical GMP auditing, including experience leading external supplier audits independently. The ideal candidate will be located near a major transportation hub in Southern California and willing to travel to support a minimum of 2 audits per month.

Key Responsibilities
  • Lead supplier audits in pharmaceutical and regulated manufacturing environments
  • Conduct audits to 21 CFR 210/211, EU GMP Vol. 4, Canada GMP, and applicable quality standards
  • Assess supplier quality systems, manufacturing controls, documentation, and compliance practices
  • Support audits involving medical device quality systems (ISO 13485 / 21 CFR 820)
  • Prepare detailed audit reports and communicate findings to stakeholders
  • Represent SQA professionally at supplier sites and client engagements
  • Support corrective action review and supplier follow-up activities as needed
Required Qualifications
  • 15+ years of experience in Quality within pharmaceutical or regulated industries
  • Minimum 5+ years performing audits as a lead auditor
  • Experience conducting external supplier audits independently
  • Strong experience with 21 CFR 210/211, EU GMP Vol. 4, and/or Canada GMP
  • Familiarity with ISO 13485 and/or 21 CFR 820
  • Strong written and verbal communication skills
  • Willingness to travel throughout Southern California and surrounding regions
  • Availability to support a minimum of 2 audits per month
Preferred Qualifications
  • Experience with ISO 17025 (Laboratories)
  • Experience auditing packaging (ISO 15378), warehousing/distribution, excipients, or APIs
  • Additional experience with Food or Animal Health standards (21 CFR 110, 111, 120, or 507)
  • Located near Los Angeles or another major Southern California transportation hub

$1,200 - $1,400 a day

$1,200 – 1,400 USD per 1‑day audit (inclusive of preparation, travel, audit execution, reporting, and follow‑up). Travel expenses reimbursed at cost with receipts per SQA travel policy. Flexible, project‑based opportunity – you may accept or decline audit assignments based on your schedule.

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.

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