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Fda Auditor Jobs in Virginia (NOW HIRING)

McKesson

Quality Assurance Auditor

Richmond, VA · Hybrid

$102K - $109K/yr

Maintain current knowledge of applicable FDA regulations, cGMP requirements, industry standards ... ISO 13485 Lead Auditor Certification - Preferred Preferred Critical Skills: * 2+ years of ...

McKesson

Quality Assurance Auditor

Richmond, VA · Hybrid

$102K - $109K/yr

Maintain current knowledge of applicable FDA regulations, cGMP requirements, industry standards ... ISO 13485 Lead Auditor Certification - Preferred Preferred Critical Skills: * 2+ years of ...

Thermo Fisher Scientific

QA Auditor I

Richmond, VA

Join us as Quality Assurance Auditor I - And play a crucial role in ensuring compliance and ... Demonstrated ability to perform GxP audits based on SOPs and applicable FDA regulations, ICH ...

Thermo Fisher Scientific

QA Auditor I

Richmond, VA · On-site

Join us as Quality Assurance Auditor I - And play a crucial role in ensuring compliance and ... Demonstrated ability to perform GxP audits based on SOPs and applicable FDA regulations, ICH ...

VB Spine

Sr. Quality Engineer

Leesburg, VA · On-site

$100K - $110K/yr

Experience interacting with regulatory agencies and supporting audits (FDA, Notified Bodies, etc ... Professional certifications (CQE, Six Sigma, Lead Auditor, etc.) are highly desirable Why VB Spine?

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Fda Auditor information

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$32.7K

$75.6K

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How much do fda auditor jobs pay per year?

As of Aug 10, 2026, the average yearly pay for fda auditor in Virginia is $75,602.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,000.00 and $97,700.00 per year, depending on experience, location, and employer.

What is an FDA auditor?

An FDA Auditor is responsible for inspecting facilities, processes, and documentation to ensure compliance with U.S. Food and Drug Administration (FDA) regulations. They review manufacturing practices, quality control systems, and regulatory filings for industries such as pharmaceuticals, medical devices, and food production. FDA Auditors may work for the FDA or for companies preparing for FDA inspections. Their role helps ensure public safety by verifying that products meet legal and quality standards.

What are the key skills and qualifications needed to thrive as an FDA auditor?

To thrive as an FDA Auditor, you need a strong background in life sciences, regulatory compliance, and audit methodologies, usually supported by a relevant degree and professional certifications such as RAC or CQA. Familiarity with FDA regulations (such as 21 CFR), electronic quality management systems (eQMS), and audit management tools is essential. Attention to detail, critical thinking, and strong communication skills help auditors navigate complex regulatory settings and interact effectively with stakeholders. These competencies are crucial for ensuring companies meet rigorous FDA standards and maintain regulatory compliance.

What do FDA auditors make?

FDA auditors typically earn a salary that ranges from $60,000 to $100,000 annually, depending on experience, location, and employer. They may also receive benefits such as health insurance, paid time off, and overtime pay, especially when conducting inspections or audits. Salaries can vary based on certifications, such as Certified Quality Auditor (CQA), and the complexity of the audits performed.

How to become an FDA auditor?

To become an FDA auditor, candidates typically need a bachelor's degree in a relevant field such as life sciences, chemistry, or pharmacy, along with experience in quality assurance or regulatory compliance. Professional certifications like Certified Quality Auditor (CQA) or training in Good Manufacturing Practices (GMP) are also valuable. Strong attention to detail, knowledge of FDA regulations, and auditing skills are essential for success in this role.

What are the primary challenges FDA auditors face during compliance inspections?

FDA Auditors often encounter challenges such as interpreting complex and evolving regulatory guidelines, managing on-site audits in diverse environments, and reviewing extensive documentation under tight timeframes. They must adapt quickly to various industry settings, handle potentially uncooperative stakeholders, and maintain objectivity throughout their evaluations. Successfully overcoming these challenges requires resilience, up-to-date regulatory knowledge, and excellent people skills. These hurdles are a vital part of ensuring public health and safety by holding organizations to the highest standards of compliance.

What are the most commonly searched types of Fda Auditor jobs in Virginia? The most popular types of Fda Auditor jobs in Virginia are:
What are popular job titles related to Fda Auditor jobs in Virginia? For Fda Auditor jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Fda Auditor jobs in Virginia look for? The top searched job categories for Fda Auditor jobs in Virginia are:
What cities in Virginia are hiring for Fda Auditor jobs? Cities in Virginia with the most Fda Auditor job openings:
Fda Auditor jobs near you
Infographic showing various Fda Auditor job openings in Virginia as of August 2026, with employment types broken down into 79% Full Time, 15% Part Time, 5% Contract, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $75,602 per year, or $36.3 per hour.

Quality Assurance Auditor

McKesson

Richmond, VA • Hybrid

$102K - $109K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 12 days ago

McKesson rating

7.9

Company rating: 7.9 out of 10

Based on 209 frontline employees who took The Breakroom Quiz

47th of 86 rated pharmaceutical

Job description

McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve - we care.

What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow's health today, we want to hear from you.

Join Our Team and Help Shape the Quality Behind McKesson Brands

Are you passionate about quality, compliance, and building trusted supplier relationships? McKesson is seeking a Quality Assurance Auditor to play a critical role in the continued growth and success of our McKesson Brands business.

In this highly visible role, you'll travel extensively to supplier manufacturing facilities across the United States and internationally, partnering directly with potential and existing suppliers to evaluate quality systems, assess manufacturing capabilities, and ensure compliance with industry regulations and McKesson quality standards. Your expertise will directly influence supplier qualification decisions that protect patients, support regulatory compliance, and help bring high-quality healthcare products to market.

This is an exciting opportunity for a quality professional who enjoys travel, values relationship building, thrives in highly regulated environments, and wants to make a meaningful impact across a growing global supplier network.

Job Summary:

The Quality Assurance Auditor supports the qualification, approval, and ongoing oversight of domestic and international suppliers that manufacture products for McKesson Brands. This role is responsible for conducting supplier quality audits, evaluating quality systems and manufacturing controls, and assessing compliance with FDA regulations, current Good Manufacturing Practices (cGMP), ISO standards, and McKesson quality requirements.

Working cross-functionally with quality, sourcing, regulatory, and supplier partners, the auditor helps ensure that suppliers have the systems, processes, and controls necessary to consistently deliver safe, effective, and compliant products. This role requires extensive travel and direct interaction with supplier leadership and quality teams to drive continuous quality improvement and supplier performance.

Key Responsibilities:

  • Conduct comprehensive on-site audits of domestic and international supplier manufacturing facilities to assess compliance with FDA regulations, cGMP requirements, ISO standards, and McKesson quality expectations.

  • Support the supplier qualification and requalification audit program by planning, coordinating, and executing audits in accordance with established schedules and quality requirements.

  • Evaluate supplier quality management systems, manufacturing processes, documentation practices, validation programs, corrective and preventive actions (CAPA), and overall regulatory compliance.

  • Identify quality, compliance, and operational risks and prepare detailed audit reports that clearly communicate observations, findings, and recommendations.

  • Partner with supplier quality teams and internal stakeholders to monitor corrective actions and ensure timely resolution of audit findings.

  • Collaborate with cross-functional teams including Quality Assurance, Regulatory Affairs, Sourcing, and Product Development to support supplier approval and ongoing supplier performance management activities.

  • Maintain current knowledge of applicable FDA regulations, cGMP requirements, industry standards, and emerging quality system expectations.

  • Represent McKesson professionally while building productive relationships with suppliers and external partners.

  • Travel approximately 75%, primarily throughout North America with occasional international travel, to conduct on-site supplier audits and assessments.

Compensation & Benefits:

McKesson offers a competitive compensation and benefits package designed to attract and reward top talent. The expected base salary range for this position is $102,000 to $109,000 annually, depending on experience, skills, geographic location, and other job-related factors.

In addition to base salary, this position is eligible for participation in the company's Annual Incentive Plan (AIP) with a target bonus opportunity of 5% of base salary, subject to plan terms and company performance.

Our comprehensive benefits package includes:

  • 16 days of Paid Time Off (PTO)

  • 5 Personal Holidays annually

  • 7 Fixed Holidays

  • 401(k) with company matching contributions

  • Medical, dental, and vision benefits

  • Health benefits effective beginning the month following hire

  • Additional wellness, financial, and professional development resources

Minimum Requirements:

4+ years of relevant experience

Education/Training/Certification:

  • Bachelor's degree in Science or related experience

  • ISO 13485 Lead Auditor Certification - Preferred

Preferred Critical Skills:

  • 2+ years of experience conducting quality audits within a highly regulated environment, including medical device, pharmaceutical, supplier qualification, quality systems, GMP/cGMP, or related regulatory compliance audits.

  • Total 4 years of professional experience in auditing, quality assurance, supplier quality, compliance, manufacturing quality, or other related quality functions.

  • Demonstrated ability to communicate audit observations, compliance findings, and quality concerns professionally and diplomatically while working on-site with supplier leadership and quality teams, fostering productive discussions and driving resolution of complex issues.

  • Experience performing supplier, quality system, cGMP, GMP, pharmaceutical, medical device, or contract manufacturing audits in a highly regulated environment.

  • Strong knowledge of FDA regulations, 21 CFR Part 820, current Good Manufacturing Practices (cGMP), ISO 13485, and quality management systems.

  • Experience evaluating supplier qualification programs, quality systems, manufacturing operations, and compliance processes.

  • Ability to identify quality risks, assess regulatory compliance, and recommend practical corrective actions.

  • Demonstrated experience writing audit reports, documenting findings, and presenting recommendations to stakeholders.

  • Strong project management and organizational skills with the ability to independently manage multiple audits and priorities.

  • Ability to travel extensively and work effectively in manufacturing, laboratory, warehouse, and office environments.

Additional Skills:

  • ASQ Certified Quality Auditor (CQA), Lead Auditor certification, or similar quality certification preferred.

  • Spanish bilingual capability a plus.

  • Bachelor's degree in chemistry, biology, microbiology, engineering, life sciences, or a related technical discipline preferred.

Work Environment/Physical Demands:

  • Will be working, standing, walking in various manufacturing areas.

  • Time spent in home office conducting computer based administrative tasks.

We are proud to offer a competitive compensation package at McKesson as part of our Total Rewards. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. The pay range shown below is aligned with McKesson's pay philosophy, and pay will always be compliant with any applicable regulations. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered. For more information regarding benefits at McKesson, pleaseclick here.

Our Base Pay Range for this position

$83,300 - $138,800

McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson's (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:
McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.


McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.

McKesson job postings are posted on our career site: careers.mckesson.com.

McKesson is an Equal Opportunity Employer

McKesson provides equal employment opportunities to applicants and employees, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other legally protected category. For additional information on McKesson's full Equal Employment Opportunity policies, visit our Equal Employment Opportunity page.

McKesson is committed to being an Equal Employment Opportunity Employer and offers opportunities to all job seekers including job seekers with disabilities. If you need a reasonable accommodation to assist with your job search or application for employment, please contact us by sending an email to (United States) Disability_Accommodation@McKesson.com or (Canada) Accessibility@mckesson.ca. Resumes or CVs submitted to this email box will not be accepted.

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