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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

Concord, NC

Onsite

Full Time

Senior

0 applicants

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About this role

A Quality Assurance professional at Lilly will support the startup and operation of a new manufacturing site in Concord, North Carolina, focusing on final batch disposition of drug products. The role ensures GMP compliance, manages site readiness plans, and oversees the approval of quality documents to facilitate regulatory approval. Collaborative efforts involve utilizing electronic batch records to maintain data integrity and ensuring safe, efficacious medication release to patients worldwide.

Responsibilities

Perform final batch disposition of semi-finished and finished drug products
Review and approve GMP documents including deviations and change controls
Support development and execution of the site readiness plan
Utilize electronic batch records to confirm manufacturing production data integrity
Ensure GMP compliance during facility qualification, validation, and startup

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.