Brandi Phillips Email and Phone Number

-Managed commercial accounts worth >$20M annual revenue, with constant focus on customer service, while driving revenue growth.-Managed pharmaceutical projects (early phase development, through process validation, commercial launch, and life cycle projects)

-Process Champion for a team that designed and implemented a Lean Lab model in Quality Operations, resulting in 60% increase in productivity and 50% decrease in cycle time for analytical release testing of finished products-Analyzed drug product using validated HPLC methods

• Conduct assays to support clinical trials in a CAP/CLIA certified, GLP compliant laboratory in the Division of Infectious Diseases.• Analyze data, perform statistical and graphical analysis of data, and interpret results.• ELISA assay development, qualification, and validation.• Author protocols, SOPs, reports and other quality documents

• Characterized polyclonal and monoclonal antibodies using RIA, ELISA, and Luminex xMAP and performed preliminary immunoassay development.• Developed and utilized HPLC methods to support R&D immunoassay development.• Performed antibody purifications from crude polyclonal and monoclonal sources.• Carried out radio-iodinations of proteins/peptides followed by purification using HPLC.

• Analyzed active pharmaceutical ingredients using validated Agilent 1100 HPLC systems.• Trained in various HPLC methods: RP, CEX, SEC and peptide mapping.• Experience with method development and qualification. • Empower software and LIMS.