Florence Qie

Associate Director, Qc Analytical Department @Atea Pharmaceuticals, Inc

Work closely with Atea Analytical/CMC to support the development, manufacturing and testing of drug substance and drug product at CDMOs. Oversee external QC testing activities including in-process, release, stability and/or method validation. • Support/lead data integrity review and oversight of external lab’s data. Perform QC review of testing records for DS and DP GMP release and stability testing to verify the data generated at the CDMO laboratory are accurate, in compliance with cGMP…