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Associate - QA Batch Disposition at Eli Lilly and Company - ApplyBlast

Associate - QA Batch Disposition

Eli Lilly and Company

4 months ago

4.0 on Glassdoor

North Carolina

Onsite

Full Time

Senior

0 applicants

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About this role

A Quality Assurance professional at Lilly will oversee the final disposition of semi-finished and finished drug combination products to ensure safe and efficacious patient outcomes. The role involves managing GMP compliance, reviewing quality documents, and supporting the startup of a new state-of-the-art manufacturing site in Concord, North Carolina. Key duties include executing batch release processes, maintaining data integrity through electronic batch records, and ensuring regulatory inspection readiness for parenteral medications and device assembly.

Responsibilities

Perform final disposition of drug product and combination product batches
Review and approve GMP documents including deviations and change controls
Support site readiness plan and development of e-release processes
Ensure high quality medicine is released to market timely
Maintain quality systems and ensure regulatory inspection readiness

Skills

Qualifications

Bachelor's degree in STEM

About Eli Lilly and Company

lilly.com

Headquarters

Indianapolis, Indiana, United States

Company Size

10001+ employees

Founded

1876

View Profile

Eli Lilly and Company is a global biopharmaceutical company headquartered in Indianapolis, Indiana. It discovers, develops, manufactures and commercializes prescription medicines across therapeutic areas including diabetes, oncology, immunology, neuroscience and pain, and has a longstanding history in insulin and other major drug discoveries. Lilly invests heavily in research and clinical development and partners with biotech, academic institutions, and industry collaborators to advance biologics, small molecules, and precision medicines. The company operates global manufacturing and commercial networks and provides patient-support programs to improve access to its therapies.