✦ Luna Orbit — QA & Testing

Associate Director Data and Systems QA

at Eli Lilly

📍 US, Lebanon IN Unknown 💰 $123K – $180K USD / year Posted March 25, 2026
Salary $123K – $180K USD / year
Type Not Specified
Experience mid
Exp. Years 5+ years
Education BS or higher degree in Engineering or science related field
Category QA & Testing

Provide quality oversight for computer system validation and data management activities at a pharmaceutical manufacturing site, ensuring compliance with GMP and regulatory standards.

  • Oversee computer system validation
  • Ensure data integrity and management
  • Support GMP manufacturing
  • Prepare for regulatory inspections
  • Mentor data and QA teams

Validation of computer systems, data integrity and management, GMP compliance, regulatory inspection readiness, data governance.

The ideal candidate is a senior QA professional with 5+ years experience in computer system validation, data integrity, and GMP within pharmaceutical manufacturing, capable of leading validation and data oversight activities.

Computer System ValidationData IntegrityData ManagementGMPRegulatory requirementsQuality Management SystemsProblem solvingDecision making
QATS/MS QCEngineering
Computer System ValidationData IntegrityData ManagementGMP
Computer System ValidationData IntegrityData ManagementGMPRegulatory requirementsQuality Management SystemsProblem solvingDecision making
Computer System ValidationData IntegrityData ManagementGMPcGMPRegulatory requirementsQuality Management SystemsProblem solvingDecision making
leadershipmentoringcollaborationtechnical supporttraining
Industry Healthcare & Medical
Job Function Quality oversight of validation and data management in pharmaceutical manufacturing
Role Subtype Quality Assurance Associate Director
Tech Domains Computer System Validation, Data Integrity, Data Management, GMP
Computer System ValidationData IntegrityData ManagementGMPcGMPregulatory inspectionsQuality AssurancevalidationData GovernanceData OversightData oversightQuality SystemsQAGxPvalidation protocolsquality systems

Lack of experience with computer system validation, No pharmaceutical or GMP background, No data integrity expertise, No leadership or mentoring experience

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