Senior GxP Quality Advisor & Audit Lead

Eli Lilly and Company; Indianapolis (IN); On-site; USD 129,000 - 211,000; Full time

Job summary

Lilly, headquartered in Indianapolis, Indiana, is seeking a Senior Advisor in Global Quality Auditing to ensure GxP compliance across development, non‑clinical and clinical programs. You will plan and execute audits, identify risks, and partner with teams to drive robust quality improvements.

The role requires a Bachelor’s degree in a scientific field, 10+ years in pharma GxP, and ability to travel up to 40%. Lilly offers comprehensive benefits and being an Equal Opportunity Employer.

Qualifications

• Bachelor’s degree in a scientific/technical discipline required.
• Minimum 10 years in pharma GxP.
• Minimum 5 years working with third-party vendors/ CROs.
• Minimum 5 years reviewing/assessing/auditing Pre‑Clinical/Clinical data.

Responsibilities

• Plan and lead complex audits and assessments of GxP operations.
• Escalate risks and compliance issues as needed.
• Meet requirements outlined in quality standards and procedures.
• Lead cross‑functional audits across multiple GxP areas.
• Educate leadership on impact of quality and data integrity issues.

Skills

Auditing

Regulatory compliance

Quality systems

Communication

Education

Bachelor’s degree in physical or biological sciences, engineering or a related scientific/technical discipline

Job description

Lilly, headquartered in Indianapolis, Indiana, is seeking a Senior Advisor in Global Quality Auditing to ensure GxP compliance across development, non‑clinical and clinical programs. You will plan and execute audits, identify risks, and partner with teams to drive robust quality improvements.

The role requires a Bachelor’s degree in a scientific field, 10+ years in pharma GxP, and ability to travel up to 40%. Lilly offers comprehensive benefits and being an Equal Opportunity Employer.