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Gmp Quality Auditor Jobs (NOW HIRING)

Interpret and apply GLP, GMP, ISO, and company quality requirements. * Conduct quality event ... Quality Auditor II * 2+ years of laboratory, quality assurance, or auditing experience in a ...

... GMP, AS, IATF, etc.) A working knowledge of calibration, inspection, measuring, and test equipment Training and certifications in Quality preferred A basic understanding of Root Cause Analysis ...

Quality Auditor Job Location: Stone Mountain, GA Reports To: Safety & Quality Supervisor Job ... Communicates accordingly on quality issues, GMP, or any other quality defects as needed. * Reviews ...

Pharmaceutical, Dietary Supplement and Cosmetic GMP Auditor - Remote Intertek, a leading provider ... Bringing quality, safety, and sustainability to life. What are we looking for? This is a full-time ...

Pharmaceutical, Dietary Supplement and Cosmetic GMP Auditor - Remote Intertek, a leading provider ... Bringing quality, safety, and sustainability to life. What are we looking for? This is a full-time ...

Quality Auditor PURPOSE: The Quality Auditor position is an entry level position that is ... Adhere to Good Manufacturing Practices (GMP) guidelines; wear protective clothing, long-sleeved ...

Quality Auditor PURPOSE: The Quality Auditor position is an entry level position that is ... Adhere to Good Manufacturing Practices (GMP) guidelines; wear protective clothing, long-sleeved ...

The Quality Auditor II reviews GLP studies for completeness, compliance, concurrence, and accuracy ... Regulatory and Policy & Procedural Guidance Know and follow GLP, GMP and relevant ISO regulations ...

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Gmp Quality Auditor information

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$12

$38

$143

How much do gmp quality auditor jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for gmp quality auditor in the United States is $38.60, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $32.69 per hour, depending on experience, location, and employer.

What is a GMP Quality Auditor?

A GMP Quality Auditor is a professional responsible for evaluating and ensuring that manufacturing processes comply with Good Manufacturing Practice (GMP) regulations. They conduct audits of facilities, processes, and documentation to verify adherence to industry standards and regulatory requirements. Their role helps ensure the safety, quality, and integrity of products, particularly in industries such as pharmaceuticals, food, and medical devices. GMP Quality Auditors provide guidance on corrective actions and help organizations maintain compliance to avoid regulatory issues.

What is the difference between Gmp Quality Auditor vs Gmp Quality Control Inspector?

AspectGmp Quality AuditorGmp Quality Control Inspector
CertificationsGMP Auditor Certification, ISO 9001GMP Inspector Certification, Quality Control Certifications
Work EnvironmentAuditing facilities, reviewing documentation, ensuring complianceInspecting products, sampling, testing, and recording quality
Employer & Industry UsagePharmaceutical, biotech, and supplement companies for compliance auditsManufacturing plants for product quality checks

Gmp Quality Auditors focus on evaluating compliance through audits and documentation review, while Gmp Quality Control Inspectors perform hands-on product testing and inspection. Both roles are essential in ensuring product safety and quality in GMP-regulated industries.

What are some common challenges faced by GMP Quality Auditors during internal audits, and how can they be addressed?

GMP Quality Auditors often face challenges such as resistance from staff, incomplete documentation, and time constraints during internal audits. Building strong communication skills and fostering a culture of quality can help auditors gain cooperation and ensure openness during interviews. Staying organized, preparing thorough checklists, and maintaining up-to-date knowledge of regulations enables auditors to efficiently identify issues and recommend effective corrective actions. Continuous professional development and collaboration with other quality and production teams are also key to overcoming these challenges.

What are the key skills and qualifications needed to thrive as a GMP Quality Auditor, and why are they important?

To thrive as a GMP Quality Auditor, you need a thorough understanding of Good Manufacturing Practices, regulatory compliance, and quality management systems, often supported by a scientific degree and relevant auditing certifications. Familiarity with audit management software, CAPA systems, and industry-specific regulations like FDA or EMA guidelines is crucial. Attention to detail, critical thinking, and effective communication are standout soft skills for this role. These skills ensure that manufacturing processes meet strict regulatory standards, safeguarding product quality and patient safety.
More about Gmp Quality Auditor jobs
Infographic showing various Gmp Quality Auditor job openings in the United States as of July 2026, with employment types broken down into 12% Locum Tenens, 78% Full Time, 7% Part Time, 2% Contract, and 1% Summer. Highlights an 87% Physical, 6% Hybrid, and 7% Remote job distribution, with an average salary of $80,278 per year, or $38.6 per hour.
Quality Auditor - Lebanon

Quality Auditor - Lebanon

Staffing Synergies

Lebanon, PA

Full-time

Posted 29 days ago


Job description

Quality Auditor

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!