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Senior Gmp Auditor Jobs in Decatur, GA (NOW HIRING)

Senior Quality Audits Specialist

Alpharetta, GA · Hybrid

$80K - $110K/yr

  • Medical

  • Retirement

  • PTO

The Sr. Quality Specialist - Global Quality Assurance Audits supports the execution and continuous ... GMP, ISO, and regulatory requirements. * Knowledge of auditing principles and corrective action ...

New

Senior Quality Audits Specialist

Alpharetta, GA · On-site

$80K - $110K/yr

  • Medical

  • Retirement

  • PTO

The Sr. Quality Specialist - Global Quality Assurance Audits supports the execution and continuous ... GMP, ISO, and regulatory requirements. * Knowledge of auditing principles and corrective action ...

Sr Process Engineer

Mcdonough, GA

$95K - $122K/yr

... auditing procedures. Areas of expertise include: Applicable materials & equipment knowledge ... Follows GMP's regarding food contact packaging as it pertains to the employee. * Follows IPC ...

Senior Gmp Auditor information

See Decatur, GA salary details

$49.8K

$88.8K

$116.7K

How much do senior gmp auditor jobs pay per year?

As of Aug 16, 2026, the average yearly pay for senior gmp auditor in Decatur, GA is $88,819.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,100.00 and $97,100.00 per year, depending on experience, location, and employer.

What is the difference between Senior Gmp Auditor vs Gmp Auditor?

AspectSenior Gmp AuditorGmp Auditor
CertificationsOften required or preferred (e.g., RAC, CQE)Typically required (e.g., RAC, CQE)
Experience3+ years in GMP auditing1-3 years in GMP auditing
Work EnvironmentLeading audits, mentoring junior staffConducting audits under supervision
ResponsibilitiesReview audit reports, train staffPerforming 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.

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 are popular job titles related to Senior Gmp Auditor jobs in Decatur, GA?

For Senior Gmp Auditor jobs in Decatur, GA, the most frequently searched job titles are:

What job categories do people searching Senior Gmp Auditor jobs in Decatur, GA look for?

The top searched job categories for Senior Gmp Auditor jobs in Decatur, GA are:

Senior Quality Audits Specialist

Clorox

Alpharetta, GA • Hybrid

$80K - $110K/yr

Full-time

Medical, Retirement, PTO

Posted 2 days ago

New


Job description

Clorox is the place that's committed to growth - for our people and our brands. Guided by our purpose and values, and with people at the center of everything we do, we believe every one of us can make a positive impact on consumers, communities, and teammates. Join our team. #CloroxIsThePlace

Your role at Clorox:

The Sr. Quality Specialist - Global Quality Assurance Audits supports the execution and continuous improvement of Clorox's Global Quality Assurance Audit Program across internal manufacturing sites, external manufacturers, suppliers, warehouses, service providers, and licensing partners. This role is responsible for coordinating audit activities, conducting QMS system audits, reviewing audit documentation, evaluating corrective actions, and maintaining audit records within the electronic Global Quality Management System (Intelex). The position partners with cross-functional stakeholders to ensure timely audit execution, consistent application of audit standards, and effective follow-up of audit findings to strengthen enterprise quality and compliance.

In this role, you will:

You will make a global impact on quality, compliance, and continuous improvement by partnering across the enterprise to execute and strengthen our audit programs.
Global Audit Execution & Coordination
  • Prepare audit documentation, agendas, reports, and supporting materials.
  • Ensure audit documentation is complete, accurate, and submitted within established timelines; audit report technical review.
  • Support audit readiness activities across the enterprise.
  • Support annual audit scheduling and planning activities.
  • Coordinate and conduct Corporate Quality Assurance Capability (QAC) audits, independently or as part of an audit team, at internal manufacturing sites, external manufacturers, suppliers, warehouses, service providers, and licensing partners.
  • National and International travel required, estimated 40%-50% travel annually; may vary with business needs.

Corrective Action Management & Audit Follow-up

  • Monitor audit findings and corrective action plans through closure.
  • Follow up with business partners and suppliers to ensure timely completion of commitments.
  • Verify objective evidence supporting corrective actions.
  • Escalate overdue or high-risk findings to leadership.
  • Maintain audit records and supporting documentation within Intelex.
Audit Program Administration & Continuous Improvement
  • Maintain audit metrics, dashboards, and program documentation.
  • Support continuous improvement of audit templates, procedures, and reporting tools.
  • Assist with audit calibration activities to promote scoring consistency.
  • Identify recurring findings and support trend analysis.
  • Participate in improvement initiatives that strengthen audit effectiveness.
  • Train other responsible parties on Intelex usage.
  • Become Trainer for the Clorox Quality Systems Elements course and/or other internal courses, as assigned.
Cross-Functional Partnership & Customer Support
  • Partner with Business Unit Quality, Procurement, External Operations, Regulatory, Supply Chain, Manufacturing, supplier contacts, and third-party audit resources.
  • Provide guidance on audit requirements, scoring methodology, and corrective action expectations.
  • Represent the audit program in project meetings, as assigned.
  • Support compliance with Corporate Global Quality Standards, GMP, ISO, GFSI, FSMA, FDA, HACCP, MoCRA, and customer requirements.
  • Ensure audit documentation meets enterprise governance expectations
  • Provide support to Sr. Manager, Global Quality Assurance Audits, as needed.

#LI-Hybrid

What we look for:

Minimum Requirements

  • Bachelor's degree in Quality, Engineering, Science, Manufacturing, or related technical discipline, or equivalent experience.
  • 5 plus years of experience in Quality Assurance, Supplier Quality, Manufacturing Quality, or Quality Auditing within a regulated manufacturing environment.
  • Experience conducting supplier, manufacturing, or quality system audits.
  • Experience managing corrective actions and audit documentation.
  • Experience in Food, Cosmetics, or other regulated consumer products.
  • Strong understanding of Quality Management Systems, GMP, ISO, and regulatory requirements.
  • Knowledge of auditing principles and corrective action processes.
  • Excellent organizational, problem-solving, and project coordination skills.
  • Strong written and verbal communication skills.
  • Ability to analyze audit findings and identify risk trends.
  • Ability to influence stakeholders without direct authority.
  • Experience with Microsoft Office and eQMS platforms.
  • Ability to travel globally up to 50% annually.

Preferred

  • Certified Quality Auditor (ASQ CQA) or similar certification.
  • Experience using Intelex or other eQMS platforms.
  • Experience supporting enterprise audit programs.
  • Knowledge of risk-based auditing principles.
  • Experience with audit reporting and performance metrics.
  • Continuous improvement experience using Lean or Six Sigma methodologies.
  • Multi-lingual

Physical Requirements

Must be physically capable of:

  • Climbing stairs
  • Sitting and walking multiple hours at a time
  • Lifting and carrying 10-20 lbs. on occasion

    Workplace type:

    Hybrid/Dynamic - 3 days in office, 2 days working from home; frequent travel

    Our values-based culture connects to our purpose and empowers people to be their best, professionally and personally. We serve a diverse consumer base which is why we believe teams that reflect our consumers bring fresh perspectives, drive innovation, and help us stay attuned to the world around us. That's why we foster an inclusive culture where every person can feel respected, valued, and fully able to participate, and ultimately able to thrive. Learn more.


    [U.S.]Additional Information:

    At Clorox, we champion people to be well and thrive, starting with our own people. To help make this possible, we offer comprehensive, competitive benefits that prioritize all aspects of wellbeing and provide flexibility for our teammates' unique needs. This includes robust health plans, a market-leading 401(k) program with a company match, flexible time off benefits (including half-day summer Fridays depending on location), inclusive fertility/adoption benefits, and more.


    We are committed to fair and equitable pay and are transparent with current and future teammates about our full salary ranges. We use broad salary ranges that reflect the competitive market for similar jobs, provide sufficient opportunity for growth as you gain experience and expand responsibilities, while also allowing for differentiation based on performance. Based on the breadth of our ranges, most new hires will start at Clorox in the first half of the applicable range. Your starting pay will depend on job-related factors, including relevant skills, knowledge, experience and location. The applicable salary range for every role in the U.S. is based on your work location and is aligned to one of three zones according to the cost of labor in your area.


    -Zone A: $90,900 - $170,100

    -Zone B: $83,400 - $155,900

    -Zone C: $75,800 - $141,700


    All ranges are subject to change in the future. Your recruiter can share more about the specific salary range for your location during the hiring process.


    This job is also eligible for participation in Clorox's incentive plans, subject to the terms of the applicable plan documents and policies.

    Please apply directly to our job postings and do not submit your resume to any person via text message. Clorox does not conduct text-based interviews and encourages you to be cautious of anyone posing as a Clorox recruiter via unsolicited texts during these uncertain times.

    To all recruitment agencies: Clorox (and its brand families) does not accept agency resumes. Please do not forward resumes to Clorox employees, including any members of our leadership team. Clorox is not responsible for any fees related to unsolicited resumes.