ZipRecruiter

Log In

1

Gmp Quality Auditor Jobs (NOW HIRING)

SQA Services

Quality Auditor - Pharmaceutical

Chicago, IL · On-site

$1.3K/day

We're hiring a Pharma Quality Auditor. This is a contract opportunity in which you will perform ... Direct audit experience to 21 CFR part 210/211, EU Vol 4, and Canada GMP * Strong communication and ...

SQA Services

Quality Auditor - Pharmaceutical

Warren, IN · Remote

$1.3K/day

We're hiring a Pharma Quality Auditor. This is a contract opportunity in which you will perform ... Direct audit experience to 21 CFR part 210/211, EU Vol 4, and Canada GMP * Strong communication and ...

SQA Services

Quality Auditor - Pharmaceutical

Carmel, IN · Remote

$1.3K/day

We're hiring a Pharma Quality Auditor. This is a contract opportunity in which you will perform ... Direct audit experience to 21 CFR part 210/211, EU Vol 4, and Canada GMP * Strong communication and ...

previous pagenext page

Showing results 21-40

All JobsGmp Quality Auditor Jobs

Gmp Quality Auditor information

See salary details

$12

$38

$143

How much do gmp quality auditor jobs pay per hour?

As of Aug 8, 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?

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
What job categories do people searching Gmp Quality Auditor jobs look for? The top searched job categories for Gmp Quality Auditor jobs are:
Gmp Quality Auditor jobs near you
Infographic showing various Gmp Quality Auditor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $80,278 per year, or $38.6 per hour.

Quality Auditor - Radiopharmaceuticals

SQA Services

Indianapolis, IN • Remote

$4.1K/wk

Full-time

Posted 9 days ago

Job description

For nearly 30 years, SQA Services has been a leading provider of managed supplier quality services, offering audits, assessments, remote surveillance, corrective actions, remediation, inspections, and engineering solutions to manufacturers across all industries. We deliver these services by deploying a network of highly skilled associates based throughout the United States and in over 90 countries worldwide, ensuring rapid on-site support at your supplier locations. Our associates are expert quality assurance professionals with extensive experience and local expertise, enabling us to represent our clients on-demand and with greater speed and efficiency than our competitors.
 
We're hiring a Supplier Quality Auditor who has experience working with radiopharmaceuticals. This is a contract opportunity in which you will perform supplier quality  audits at various suppliers in the Midwest. These audits are generally 1-2 days long. You are given the flexibility to accept or reject these assignments according to your own availability. 
Key Responsibilities
  • Perform supplier audits at various sites within your region of residence
  • Assure quality in the supply chains of various clients within the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries
  • Coordinate, prepare, execute, and deliver supplier audits based on your own and the client schedule
  • Utilize your regulatory knowledge of various standards from ISO, CFR, FDA, etc...
  • Respond to the Content team in a timely manner regarding edits/questions to your audit report
  • Write audit reports in accordance with client specifications
Required Qualifications
  • 5+ years of hands-on audit experience in pharmaceutical, medical device, and/or biologics industries
  • Has been the lead auditor in at least 10 audits
  • Direct audit experience to 21 CFR part 210/211, EU Vol 4, and Canada GMP
  • Strong communication and writing skills
  • Proven ability to deescalate workplace conflicts effectively
  • Ability to adapt to new technology and software.
  • Willingness to travel regionally
Preferred Qualifications
  • Direct audit experience to ISO 17025, ISO 15378, IPEC GDP, ICH Q7, ISO 13485, 21 CFR 100, and/or 21 CFR 507
  • ISO certifications are a plus but not mandatory
$4,100 - $4,100 one-time
Pay Rate: 
 
$4100 for a 3-day audit. Includes: Time spent preparing for the audit, traveling, performing the audit, writing the report, and responding to questions from our Content team of editors and the client until the report is finalized. Does not include: Following up on CAPA for any findings or reimbursement for travel expenses - expenses are reimbursed at cost with receipts per SQA travel policy. Note that SQA helps with the preparation of the audit and proofreads all audit reports.
 
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.
 
#ZR
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. 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.
apply for this job

Apply