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Pharmaceutical Gmp Auditor Jobs (NOW HIRING)

Lancesoft INC

Quality Auditor Manager

Exton, PA · On-site

$70 - $75/hr

Lead and conduct GMP audits and internal site audits. * Support global audit programs, schedules ... Strong knowledge of pharmaceutical/biotech quality and regulatory requirements. * Excellent ...

New

Global Placement Firm

Sr. Auditor

Paramus, NJ · On-site

$67/hr

Sr. Auditor Quality Assurance (Pharmaceuticals) Location: Paramus, NJ (100% On-Site) - 5 month ... pharmaceutical QA experience (with at least 2 years conducting audits) Proven understanding of GMP ...

Pharmavise

GMP Professionals

Maple Grove, MN · On-site

From development to commercialization, we partner with Pharmaceutical, Medical Device and ... Auditing experience and knowledge of audit principles and practices preferred. * Regulatory affairs ...

Vaxcyte

Manager, Supplier & Internal Auditor

San Carlos, CA · On-site +1

$151K - $176K/yr

The ideal candidate is a certified auditor with strong working knowledge of GMP, GLP, GCP, ICH, and ISO 13485 requirements and experience auditing within the pharmaceutical, biotechnology, or medical ...

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Pharmaceutical Gmp Auditor information

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How much do pharmaceutical gmp auditor jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for pharmaceutical 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 pharmaceutical GMP auditor?

Pharmaceutical GMP Auditors are professionals responsible for evaluating and ensuring that pharmaceutical manufacturing facilities comply with Good Manufacturing Practice (GMP) regulations. They conduct audits, inspect processes, review documentation, and identify areas for improvement to maintain product quality and patient safety. Their work helps companies meet regulatory standards set by authorities like the FDA or EMA, reducing the risk of product recalls or regulatory actions.

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

To thrive as a Pharmaceutical GMP Auditor, you need a strong understanding of Good Manufacturing Practice regulations, quality management systems, and a background in life sciences or pharmacy, often supported by relevant certifications. Familiarity with auditing tools, regulatory guidelines (like FDA or EMA), and quality management software is typically required. Excellent attention to detail, analytical thinking, and effective communication are crucial soft skills for conducting thorough audits and reporting findings. These skills and qualities ensure regulatory compliance, product quality, and operational integrity in pharmaceutical manufacturing environments.

What are some common challenges pharmaceutical GMP auditors face when conducting audits at multiple facilities?

Pharmaceutical GMP Auditors frequently encounter challenges such as adapting to different facility cultures, varying documentation systems, and diverse interpretations of regulatory requirements. Each site may have unique processes and levels of GMP maturity, requiring auditors to quickly adjust their approach while maintaining consistency and objectivity. Additionally, auditors often need to manage tight schedules and communicate findings diplomatically to ensure corrective actions are understood and implemented effectively.

What is the difference between Pharmaceutical Gmp Auditor vs Quality Control Analyst?

AspectPharmaceutical Gmp AuditorQuality Control Analyst
CertificationsGMP auditing certifications, relevant pharmaceutical quality certificationsLaboratory certifications, analytical testing certifications
Work EnvironmentAudit sites, manufacturing facilities, compliance departmentsLaboratories, testing facilities, production lines
Employer & Industry UsagePharmaceutical companies, contract research organizations, regulatory agenciesPharmaceutical companies, biotech firms, quality testing labs

Pharmaceutical Gmp Auditors focus on evaluating compliance with GMP regulations through site inspections, while Quality Control Analysts perform laboratory testing to ensure product quality. Both roles are essential in pharmaceutical quality assurance but differ in their primary responsibilities and work environments.

More about Pharmaceutical Gmp Auditor jobs

What states have the most Pharmaceutical Gmp Auditor jobs?

States with the most job openings for Pharmaceutical Gmp Auditor jobs include:

What job categories do people searching Pharmaceutical Gmp Auditor jobs look for?

The top searched job categories for Pharmaceutical Gmp Auditor jobs are:

Pharmaceutical Gmp Auditor jobs near you
Infographic showing various Pharmaceutical Gmp Auditor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $39,947 per year, or $19.2 per hour.

Quality Auditor Manager

Lancesoft INC

Exton, PA • On-site

$70 - $75/hr

Full-time

Posted 2 days ago

New

Job description

Manager, Quality Auditing – Contractor

Location: Exton, PA 19341
Contract: 12 Months | Schedule: Mon–Fri, 40 hrs/week
Pay: $75.74/hr on W2


Position Summary

Seeking an experienced Quality Auditing Manager to support global GMP audit programs and conduct risk-based audits of CMOs, laboratories, warehouses, suppliers, and internal sites.


Key Responsibilities

  • Lead and conduct GMP audits and internal site audits.
  • Support global audit programs, schedules, procedures, and auditor training.
  • Prepare audit reports and manage findings through closure.
  • Support inspection readiness and FDA/EMA inspections.
  • Evaluate supplier GMP compliance and support supplier qualification.
  • Maintain audit records in Track Wise or similar quality systems.


Must Have

  • Strong GMP auditing experience.
  • Experience leading audits in sterile manufacturing and biologics.
  • Experience with software validation / Computer System Validation (CSV) and computerized systems compliance.
  • Strong knowledge of pharmaceutical/biotech quality and regulatory requirements.
  • Excellent communication and audit-reporting skills.


Preferred

  • Bachelor's degree in Life Sciences, Quality, Pharmacy, Engineering, or related field.
  • Experience with FDA/EMA inspections and TrackWise.
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About LanceSoft

Sourced by ZipRecruiter

Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

Herndon, VA, US

Year founded

2000

Social media

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