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Gmp Auditor Jobs (NOW HIRING)

Revance

Supplier Quality Auditor

Johnson City, TN · On-site

The Supplier Quality Auditor is responsible for executing risk-based GMP audit programs supporting OTC and cosmetic operations. They will ensure compliance with 21 CFR 210/211, ISO 22716, and ...

Apple

Senior Lead Auditor - Medical Devices

Cupertino, CA · On-site

$99K - $122K/yr

ISO 13485, MDSAP requirements, China GMP, EU MDR, China GMP, etc...) Excellent written and verbal ... software medical device products Lead auditor certification or internal auditor ...

Innovative Skincare

Quality Auditor

Mesa, AZ · On-site

$22 - $24/hr

Ensure all work follows GMP, SOP, and company safety rules. * And other duties assigned by the Site ... in quality assurance, auditing, or manufacturing preferred. * Knowledge of GMP, SOPs, and ...

Innovative Skincare

Quality Auditor

Mesa, AZ · On-site

$22 - $24/hr

Ensure all work follows GMP, SOP, and company safety rules. * And other duties assigned by the Site ... in quality assurance, auditing, or manufacturing preferred. * Knowledge of GMP, SOPs, and ...

Apple

Senior Lead Auditor - Medical Devices

Cupertino, CA · On-site

$146K - $244K/yr

The Senior Lead Auditor will lead and maintain a risk based internal & supplier audit program to ... ISO 13485, MDSAP requirements, China GMP, EU MDR, China GMP, etc...) Excellent written and verbal ...

Sotera Health

Quality Auditor I

Nelson, NE · On-site

The auditor provides regulatory and policy and procedural guidance. The auditor collaborates with ... Know and follow GLP, GMP and relevant ISO regulations * Perform quality event investigations and ...

Maleko Personnel

Be Seen First

Protocol Auditor - Semiconductor Manufacturing

Boise, ID · On-site

$20 - $23/hr

The Protocol Auditor will be responsible for conducting internal and supplier audits, evaluating ... Support compliance with ISO 9001, IATF 16949, GMP, and other applicable semiconductor industry ...

Sotera Health

Quality Auditor I

Nelson, NE · On-site

The auditor provides regulatory and policy and procedural guidance. The auditor collaborates with ... Know and follow GLP, GMP and relevant ISO regulations * Perform quality event investigations and ...

Sotera Health

Quality Auditor I

Nelson, NE · On-site

The auditor provides regulatory and policy and procedural guidance. The auditor collaborates with ... Regulatory and Policy & Procedural Guidance Know and follow GLP, GMP and relevant ISO regulations ...

synergy

QA Lead Auditor

Dallas, TX · On-site

QA Lead Auditor - With Previous FDA Audit Experience. This position will be responsible for ... GMP requirements is required. • Minimum of a BS degree in science with a minimum of 5+ years of ...

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How much do gmp auditor jobs pay per hour?

As of Jun 10, 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 are the key skills and qualifications needed to thrive in the Gmp Auditor position, and why are they important?

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.

What does a typical day look like for a GMP Auditor?

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 is a GMP Auditor job?

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.

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Gmp Auditor jobs near you
Supplier Quality Auditor

Supplier Quality Auditor

Revance

Johnson City, TN • On-site

Full-time

Medical, Life, Retirement, PTO

Posted 11 days ago

Job description

Job Summary:
The Supplier Quality Auditor is responsible for executing risk-based GMP audit programs supporting OTC and cosmetic operations. They will ensure compliance with 21 CFR 210/211, ISO 22716, and internal quality systems. They will lead supplier, CMO, and internal audits, including routine, for-cause, and surveillance activities. They will support inspection readiness and continuous improvement activities.
Reporting to: Quality Assurance Manager, CMOs
Location: Johnson City, TN - onsite
Responsibilities/Essential Duties:
  • Execute risk-based GMP audits (supplier, CMO, internal, for-cause, surveillance).
  • Perform gap assessments and compliance evaluations aligned with regulatory standards.
  • Identify, document, and assess audit findings with appropriate risk ratings.
  • Drive and track CAPA, SCAR, and deviation resolution.
  • Support inspection readiness, including mock audits and audit hosting activities.
  • Provide cross-functional GMP and quality compliance support.
  • Support change control, document control, and training processes.
  • Ensure compliance with QMS requirements.
  • Understand tracking and trending data for Quality Compliance.
  • Analyze and trend quality data to support continuous improvement.

Basic Qualifications:
  • Bachelor's degree & 3-5 years' directly related experience, or an equivalent combination of education and experience.
  • Travel up to 50%.

Preferred Qualifications:
  • 3-5 years' GMP Quality/Auditing experience (OTC, cosmetic, or pharmaceutical).
  • Strong knowledge of GMP regulations and quality systems.
  • Effective audit execution and technical writing skills.
  • Strong analytical and problem-solving abilities.
  • Excellent communication and cross-functional collaboration skills.

Company Summary:
Crown is a proud member of the Revance Portfolio of skincare offerings. Revance is a global company developing, producing, and distributing industry-leading, differentiated products across aesthetics, skincare, and therapeutics. Revance drives innovation beyond convention to offer treatment options for individuals across generations. The Company's vision is to redefine excellence in aesthetics, skincare, and therapeutics through science-powered innovation, with an unwavering commitment to its providers, patients, and consumers. Revance's award-winning products are the result of robust research and development, a cornerstone for the Company, driven by renowned scientists. For more information about Revance, please visit us at www.revance.com.
What Revance invests in you:
  • Competitive Compensation including base salary and annual performance bonus.
  • Flexible PTO, holidays, and parental leave.
  • Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more!

Work Environment & Physical Requirements
This position requires extended periods of standing and walking on a manufacturing floor environment. Protective equipment (safety glasses, hearing protection, gowning) must be worn as required. The role operates in a temperature-controlled pharmaceutical manufacturing facility. Occasional lifting of up to 30 lbs may be required. Must be available to respond to critical shift issues outside of scheduled hours on an as-needed basis.
This section of the job description is required by the American with Disability Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a "qualified individual with a disability" in all aspects of the employment relationship. A "qualified individual with a disability" is "an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job."
Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

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