Quality Assurance Auditor

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.

Quality Assurance Auditor

Location: Richmond, VA

Travel: 50%–75% (primarily domestic, some international)

Career Level: IC-Professional-P3

Base Pay Range: $81,000 – $135,000 annually

Bonus: Eligible for annual bonus and comprehensive benefits

Position Summary

Join McKesson as a Quality Assurance Auditor supporting our global audit program for both domestic and international suppliers. This role ensures compliance with FDA regulations and current Good Manufacturing Practices (cGMP) through initial qualification audits and ongoing requalification audits. You will play a critical role in maintaining quality standards and regulatory compliance across our supply chain.

Key Responsibilities

• Execute audit program activities to ensure all audits are completed on schedule
• Perform full audits of vendor manufacturing facilities for compliance with FDA regulations and cGMP
• Document findings and collaborate with suppliers to address corrective actions
• Travel extensively (50%–75%) to supplier sites, primarily domestic with some international
  
  
  

Additional Responsibilities

• Support continuous improvement of audit processes
• Maintain accurate audit records and reports
• Collaborate with internal stakeholders to ensure quality and compliance objectives are met
  
  
  

Qualifications

• Education: Bachelor’s degree in Science or related field
• Experience:
• 2 years in medical device or pharmaceutical auditing, or quality assurance in a regulated environment
• Experience performing cGMP audits of manufacturers
• Project management experience preferred
• Knowledge & Skills:
• Strong understanding of cGMP, 21 CFR 820, ISO 13485
• Excellent communication skills (written and verbal)
• Detail-oriented with ability to follow procedures
• Spanish bilingual strongly preferred
• Technical: Proficiency in Microsoft Office Suite
  
  

Work Environment

• Combination of office and manufacturing environments
• Requires ability to travel frequently and work independently
  
  
  

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, please click here.

Our Base Pay Range for this position

$81,000 - $135,000

McKesson is an Equal Opportunity Employer

McKesson provides equal employment opportunities to applicants and employees and is committed to a diverse and inclusive environment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age or genetic information. For additional information on McKesson’s full Equal Employment Opportunity policies, visit our Equal Employment Opportunity page.

Join us at McKesson!