✦ Luna Orbit — QA & Testing

Quality Assurance - Material/Supplier Management

at Eli Lilly

📍 US, Lebanon IN Unknown 💰 $101K – $148K USD / year Posted March 20, 2026
Salary $101K – $148K USD / year
Type Not Specified
Experience mid
Exp. Years 3+ years
Education Bachelor's degree in a science, engineering, computer, or pharmaceutical related field of study or equivalent industry experience
Category QA & Testing

This role involves overseeing material and supplier management processes in a GMP environment, ensuring compliance, quality, and regulatory readiness.

  • Conduct risk assessments
  • Manage supplier qualification
  • Perform batch disposition
  • Ensure GMP compliance
  • Support regulatory inspections

The technical scope includes GMP standards, SAP systems, risk assessments, and batch disposition processes within a pharmaceutical manufacturing setting.

The ideal candidate is an experienced QA professional with at least 3 years in pharmaceutical quality assurance, familiar with GMP standards, supplier management, and regulatory compliance. They should have a strong background in material and batch management within a GMP environment.

Bachelor's degree in a scienceengineeringcomputeror pharmaceutical related field3+ years working in the pharmaceutical industryMaterial/Supplier ManagementGMP documentationRisk assessmentBatch disposition
experience with SAPregulatory inspectionsdata metrics reportingGMP documentation review
SAPGMP documentation systemsRisk assessment tools
GMPMaterial ManagementSupplier QualificationBatch DispositionRisk AssessmentSAPRegulatory ComplianceData CollectionData Analysis
Quality Management SystemsGMPSAPBatch DispositionSupplier QualificationRisk AssessmentData CollectionRegulatory ComplianceData Analysis
collaborationattention to detailcommunicationproblem-solvingteamwork
Industry Healthcare & Medical
Job Function Quality assurance and material management in pharmaceutical manufacturing
Role Subtype Supply Chain & Procurement
Tech Domains SAP
Quality AssuranceMaterial ManagementSupplier QualificationGMPBatch DispositionRisk AssessmentSAPRegulatory ComplianceData CollectionData AnalysisPharmaceuticalQuality StandardsInspection SupportGMP DocumentationMaterial ReceiptRegulatory inspectionsData metricsQuality assurancepharmaceutical

No GMP or pharmaceutical experience, Lack of GMP documentation knowledge, Less than 3 years industry experience, No GMP or GMP-related certifications

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