Lexington, KY | Full Time
$65k-86k (estimate)
Just Posted
Execute routine and non-routine testing to support manufacturing, validation, and development studies, including drug substance and drug product samples, stability testing, and various protocol studies. Maintain GMP compliance and operational readiness of QC areas, ensuring adherence to industry standards. Manage critical reagent inventory, including antibodies and cell banks, ensuring appropriate quantities are available for testing. Assist in s...