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Gmp Auditor Jobs (NOW HIRING)

Staffing Synergies

Quality Auditor - Edison

Edison, NJ · On-site

$18/hr

Quality Auditor Location: Edison, NJ Pay: $18/hr Shift: 1st shift - 6:00am-2:45pm 2nd shift - 3 ... What We're Looking For: * 5+ years of GMP/QA experience in a manufacturing environment (or ...

Staffing Synergies

Quality Auditor - Edison

Edison, NJ · On-site

$18/hr

Quality Auditor Location: Edison, NJ Pay: $18/hr Shift: 1st shift - 6:00am-2:45pm 2nd shift - 3 ... What We're Looking For: * 5+ years of GMP/QA experience in a manufacturing environment (or ...

Staffing Synergies

Quality Auditor - Edison

Edison, NJ · On-site

$18/hr

Quality Auditor Location: Edison, NJ Pay: $18/hr Shift: 1st shift - 6:00am-2:45pm 2nd shift - 3 ... What We're Looking For: * 5+ years of GMP/QA experience in a manufacturing environment (or ...

Staffing Synergies

QA Auditor - Detroit

Detroit, MI

$18/hr

We are looking for a detail-oriented, proactive, and collaborative Quality Assurance Auditor to ... Perform Good Manufacturing Practices (GMP) and Standard Operating Procedure (SOP) conformance ...

Pfizer

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Proven knowledge and experience in GMP/GDP auditing of at least 3 technology areas. * Demonstrated ability to apply the following competencies and soft skills: business skills (negotiation, logical ...

Pfizer

Audit Lead

Michigan, ND · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Proven knowledge and experience in GMP/GDP auditing of at least 3 technology areas. * Demonstrated ability to apply the following competencies and soft skills: business skills (negotiation, logical ...

Pfizer

Audit Lead

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Proven knowledge and experience in GMP/GDP auditing of at least 3 technology areas. * Demonstrated ability to apply the following competencies and soft skills: business skills (negotiation, logical ...

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Gmp Auditor information

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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.

Quality Auditor - Edison

Staffing Synergies

Edison, NJ • On-site

$18/hr

Other

This job post has expired today. Applications are no longer accepted.

Job description

Quality Auditor

Location: Edison, NJ

Pay: $18/hr

Shift:

1st shift - 6:00am-2:45pm

2nd shift - 3:00pm-11:45pm

Join Our Team at Staffing Synergies!
We are looking for a detail-oriented Quality Auditor to join our team. In this role, you’ll play a key part in ensuring that our products meet the highest standards of quality, safety, and compliance. If you thrive in a fast-paced environment and take pride in precision, this is the opportunity for you!

What You’ll Do:

  • Perform quality inspections on production lines to ensure compliance with FDA, cGMP, SOPs, and customer requirements.
  • Partner with Production and Quality Management to resolve quality issues in real time.
  • Conduct inspections, audits, and Acceptance Quality Limits (AQL) checks to verify product integrity.
  • Confirm and record date codes, lot numbers, expiration dates, and labeling accuracy.
  • Place non-conforming materials in quarantine and document all deviations.
  • Monitor batch records, validation protocols, and ensure proper documentation is completed.

What We’re Looking For:

  • 5+ years of GMP/QA experience in a manufacturing environment (or equivalent relevant experience).
  • Strong knowledge of FDA and cGMP regulations.
  • Excellent communication, problem-solving, and teamwork skills.
  • Ability to work independently, manage multiple tasks, and adapt to changing priorities.
  • High School Diploma or GED required.
  • Bilingual a plus!

Physical Requirements:

  • Ability to stand for long periods (8+ hours).
  • Able to lift up to 25 lbs occasionally.
  • Comfortable with bending, squatting, reaching, and repetitive hand/finger use.

If you’re passionate about quality and want to make an impact, apply today!