$125 - $150/hr
Formal auditor training (ISO 13485, GMP) required or equivalent experience; Lead Auditor certification preferred. * 5-8 years in Supplier Quality/Quality Engineering in medical device and/or pharma.
$125 - $150/hr
Formal auditor training (ISO 13485, GMP) required or equivalent experience; Lead Auditor certification preferred. * 5-8 years in Supplier Quality/Quality Engineering in medical device and/or pharma.
... Senior Quality Engineer Responsibilities ... Quality Oversight & GMP Operations * Provide Quality Assurance oversight for GMP manufacturing ...
Quick apply
... Senior Quality Engineer Responsibilities ... Quality Oversight & GMP Operations * Provide Quality Assurance oversight for GMP manufacturing ...
... Senior Quality Engineer Responsibilities ... Quality Oversight & GMP Operations * Provide Quality Assurance oversight for GMP manufacturing ...
... Senior Quality Engineer Responsibilities ... Quality Oversight & GMP Operations * Provide Quality Assurance oversight for GMP manufacturing ...
Sr. Project Manager - Preconstruction and Cost Estimating, Facility Development
Orlando, FL · On-site
Senior Level Preconstruction and Cost Estimating Manager Position reporting to VP of Facility ... GMP contracts and needed ODP credits and close outs. • Manage and engage project cost auditing ...
Sr. Project Manager - Preconstruction and Cost Estimating, Facility Development
Orlando, FL · On-site
Senior Level Preconstruction and Cost Estimating Manager Position reporting to VP of Facility ... GMP contracts and needed ODP credits and close outs. • Manage and engage project cost auditing ...
Senior Analytical Chemist
Burbank, CA · On-site
FSNS Certification & Audit - Provides accredited third-party auditing and certification services, including food safety, animal welfare, and GMP programs. Summary We are currently seeking a Senior ...
Senior Analytical Chemist
Burbank, CA · On-site
FSNS Certification & Audit - Provides accredited third-party auditing and certification services, including food safety, animal welfare, and GMP programs. Summary We are currently seeking a Senior ...
Senior Level Preconstruction and Cost Estimating Manager Position reporting to VP of Facility ... GMP contracts and needed ODP credits and close outs. • Manage and engage project cost auditing ...
Senior Level Preconstruction and Cost Estimating Manager Position reporting to VP of Facility ... GMP contracts and needed ODP credits and close outs. • Manage and engage project cost auditing ...
FSNS Certification & Audit - Provides accredited third-party auditing and certification services, including food safety, animal welfare, and GMP programs. Summary We are currently seeking a Senior ...
Quick apply
FSNS Certification & Audit - Provides accredited third-party auditing and certification services, including food safety, animal welfare, and GMP programs. Summary We are currently seeking a Senior ...
... auditing program. * Ensures controlled documentation is generated, revised, approved, and ... Prior GMP experience is required; prior CDMO experience preferred. * Prior experience with GMP ...
... auditing program. * Ensures controlled documentation is generated, revised, approved, and ... Prior GMP experience is required; prior CDMO experience preferred. * Prior experience with GMP ...
... auditing program. * Ensures controlled documentation is generated, revised, approved, and ... Prior GMP experience is required; prior CDMO experience preferred. * Prior experience with GMP ...
... auditing program. * Ensures controlled documentation is generated, revised, approved, and ... Prior GMP experience is required; prior CDMO experience preferred. * Prior experience with GMP ...
... auditing program. * Ensures controlled documentation is generated, revised, approved, and ... Prior GMP experience is required; prior CDMO experience preferred. * Prior experience with GMP ...
... auditing program. * Ensures controlled documentation is generated, revised, approved, and ... Prior GMP experience is required; prior CDMO experience preferred. * Prior experience with GMP ...
The Senior Manager, GxP Computerized Systems Auditing, is responsible for managing and executing a ... S., EU, China, and other global GMP/GDP requirements, as well as ICH expectations relevant to ...
The Senior Manager, GxP Computerized Systems Auditing, is responsible for managing and executing a ... S., EU, China, and other global GMP/GDP requirements, as well as ICH expectations relevant to ...
The Senior Manager, GxP Computerized Systems Auditing, is responsible for managing and executing a ... S., EU, China, and other global GMP/GDP requirements, as well as ICH expectations relevant to ...
The Senior Manager, GxP Computerized Systems Auditing, is responsible for managing and executing a ... S., EU, China, and other global GMP/GDP requirements, as well as ICH expectations relevant to ...
Job Opportunity :: API Manufacturing Facility :: Rensselaer, NY
Rensselaer, NY · On-site
$74K - $95K/yr
... GMP manufacturing environments. This is a hands on operational role, not a senior management or pure compliance/auditor position. The ideal candidate should have direct experience supporting ...
Quick apply
Job Opportunity :: API Manufacturing Facility :: Rensselaer, NY
Rensselaer, NY · On-site
$74K - $95K/yr
... GMP manufacturing environments. This is a hands on operational role, not a senior management or pure compliance/auditor position. The ideal candidate should have direct experience supporting ...
... GMP manufacturing environments. This is a hands on operational role, not a senior management or pure compliance/auditor position. The ideal candidate should have direct experience supporting ...
Quick apply
... GMP manufacturing environments. This is a hands on operational role, not a senior management or pure compliance/auditor position. The ideal candidate should have direct experience supporting ...
Senior Engineer I, Validation
Bothell, WA · On-site
This position requires a hands-on validation engineer with experience in GMP, an understanding of ... and auditors. * Executes multiple projects that require qualification work arising from change ...
Senior Engineer I, Validation
Bothell, WA · On-site
This position requires a hands-on validation engineer with experience in GMP, an understanding of ... and auditors. * Executes multiple projects that require qualification work arising from change ...
Senior Engineer I, Validation
Bothell, WA · On-site
This position requires a hands-on validation engineer with experience in GMP, an understanding of ... and auditors. * Executes multiple projects that require qualification work arising from change ...
Senior Engineer I, Validation
Bothell, WA · On-site
This position requires a hands-on validation engineer with experience in GMP, an understanding of ... and auditors. * Executes multiple projects that require qualification work arising from change ...
... with auditors. * Prepare audit-ready documentation and ensure site/functional readiness through ... Ensure ongoing compliance with applicable regulations (e.g., GMP, GLP, GCP as applicable) and ...
... with auditors. * Prepare audit-ready documentation and ensure site/functional readiness through ... Ensure ongoing compliance with applicable regulations (e.g., GMP, GLP, GCP as applicable) and ...
Sr. Compliance Specialist
Saint Louis, MO · On-site
... with auditors. * Prepare audit-ready documentation and ensure site/functional readiness through ... Ensure ongoing compliance with applicable regulations (e.g., GMP, GLP, GCP as applicable) and ...
Sr. Compliance Specialist
Saint Louis, MO · On-site
... with auditors. * Prepare audit-ready documentation and ensure site/functional readiness through ... Ensure ongoing compliance with applicable regulations (e.g., GMP, GLP, GCP as applicable) and ...
... GMP manufacturing, testing, and clinical activities. Reporting directly to the Quality Officer ... Demonstrated experience auditing contract manufacturers, testing labs, depot, or CROs, and ...
... GMP manufacturing, testing, and clinical activities. Reporting directly to the Quality Officer ... Demonstrated experience auditing contract manufacturers, testing labs, depot, or CROs, and ...
... GMP manufacturing, testing, and clinical activities. Reporting directly to the Quality Officer ... Demonstrated experience auditing contract manufacturers, testing labs, depot, or CROs, and ...
... GMP manufacturing, testing, and clinical activities. Reporting directly to the Quality Officer ... Demonstrated experience auditing contract manufacturers, testing labs, depot, or CROs, and ...
Senior Gmp Auditor information
See salary details
$51K - $57.2K
1% of jobs
$57.2K - $63.5K
2% of jobs
$63.5K - $69.7K
4% of jobs
$69.7K - $75.9K
7% of jobs
$80.6K is the 25th percentile. Wages below this are outliers.
$75.9K - $82.1K
14% of jobs
$82.1K - $88.4K
17% of jobs
The median wage is $89.7K / yr.
$88.4K - $94.6K
22% of jobs
$97.8K is the 75th percentile. Wages above this are outliers.
$94.6K - $100.8K
15% of jobs
$100.8K - $107K
8% of jobs
$107K - $113.3K
6% of jobs
$113.3K - $119.5K
3% of jobs
$51K
$91K
$119.5K
How much do senior gmp auditor jobs pay per year?
As of Aug 16, 2026, the average yearly pay for senior gmp auditor in the United States is $90,973.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $99,500.00 per year, depending on experience, location, and employer.
What is a senior GMP auditor?
Senior GMP Auditors are experienced professionals responsible for evaluating and ensuring that pharmaceutical, biotechnology, and medical device companies comply with Good Manufacturing Practices (GMP) regulations. They conduct thorough audits of manufacturing processes, documentation, and quality management systems to identify areas of non-compliance and recommend corrective actions. Senior GMP Auditors often lead audit teams, mentor junior auditors, and communicate findings to regulatory authorities and company leadership. Their work is critical for ensuring product safety, quality, and regulatory compliance.
What are the key skills and qualifications needed to thrive as a senior GMP auditor?
To thrive as a Senior GMP Auditor, you need in-depth knowledge of Good Manufacturing Practices, regulatory compliance, and quality management systems, typically supported by a science degree and substantial experience in pharmaceutical or biotech industries. Proficiency with audit management software, documentation systems, and relevant certifications such as ASQ Certified Quality Auditor (CQA) are highly valued. Exceptional attention to detail, analytical thinking, and strong communication skills distinguish top performers in this role. These skills are crucial for ensuring regulatory adherence, maintaining product quality, and mitigating compliance risks within highly regulated environments.
What are the most common challenges faced by a senior GMP auditor during site inspections?
Senior GMP Auditors often encounter challenges such as navigating varying levels of GMP awareness across different facilities, managing tight audit schedules, and ensuring clear communication with diverse teams. They must remain objective while diplomatically addressing compliance gaps, sometimes in high-pressure environments. Additionally, balancing thorough documentation with efficient time management is key to delivering actionable audit reports that help organizations improve their quality systems.
What is the difference between Senior Gmp Auditor vs Gmp Auditor?
| Aspect | Senior Gmp Auditor | Gmp Auditor |
|---|---|---|
| Certifications | Often required or preferred (e.g., RAC, CQE) | Typically required (e.g., RAC, CQE) |
| Experience | 3+ years in GMP auditing | 1-3 years in GMP auditing |
| Work Environment | Leading audits, mentoring junior staff | Conducting audits under supervision |
| Responsibilities | Review audit reports, train staff | Performing audits, preparing reports |
The main difference is experience and responsibility level. Senior Gmp Auditors typically have more experience, lead audits, and mentor others, while Gmp Auditors focus on executing audits under supervision. Both roles require similar certifications and work within GMP environments in the pharmaceutical and biotech industries.
More about Senior Gmp Auditor jobs
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The most popular types of Gmp Auditor jobs are:
What states have the most Senior Gmp Auditor jobs?
States with the most job openings for Senior Gmp Auditor jobs include:
What job categories do people searching Senior Gmp Auditor jobs look for?
The top searched job categories for Senior Gmp Auditor jobs are:
$125 - $150/hr
Other
Posted 11 days ago
Job description
Description:
#J-18808-LjbffrLead supplier quality activities to ensure externally supplied materials, components, and services meet GMP, ISO 13485, and internal standards. Support the audit program, CAPA follow-up, and Quality Technical Agreements (QTAs) in partnership with Supplier Owner and cross-functional teams.
Location: Warren, New Jersey - 3 days on site & 2 days remote
Salary Range: 125k-150k
Key Responsibilities:- Support the audit program: annual plan, execution, reporting, and follow-up of CAPA effectiveness.
- Maintain supplier risk assessment, segmentation, and performance reviews; drive improvement actions with suppliers.
- Lead QTA lifecycle: creation, review, negotiation support with Procurement, and periodic updates; ensure RACI is defined and applied.
- Support SOPs for Supplier Management and ensure alignment with global procedures, coach teams on process adherence.
- Ensure readiness for inspections (e.g., FDA, EU) and PAI: maintain supplier files GMP certificates, monitor expirations, and prepare audit/inspection evidence.
- Provide quality engineering support (incoming controls, sampling plans, problem solving 8D/5Why, data analysis) to prevent recurrence of issues.
- Bachelor’s degree in Engineering, Life Sciences, Pharmacy or related field (Master’s preferred).
- Formal auditor training (ISO 13485, GMP) required or equivalent experience; Lead Auditor certification preferred.
- 5–8 years in Supplier Quality/Quality Engineering in medical device and/or pharma. Pharma/Biologics preferred.
- Proven experience leading supplier audits, managing CAPA, and implementing QTAs.
- Working knowledge of FDA 21 CFR Parts 820/210/211/600/610/680, EU GMP, ISO 13485, ISO 14971.
- Experience with eQMS (Veeva or ENNOV is a +), supplier performance dashboards, and RACI implementation.
- Fluent in English; strong communication and stakeholder influencing skills.
- Curiosity: Keep on exploring uncharted territories. Always ask “why?” and more importantly “why not?”
- Courage: Take smart risks, mentor each other to always do better & be accountable for our choices, our opinions, and our actions.
- Collaboration: Teamwork and spirit. Support each other and be equally involved in the achievement of our common goals.
- Credibility: Be transparent, follow through and build trust. Educate ourselves about our unique technology.