NGUYEN THANH

• Developing and validating analytical methods for drug products • Setting a new analytical Laboratory from the first step following GLP • Directly controlling standards for starting material and testing finished products using HPLC, FT-IR, GC, Titration, KF • Write the registration doses of a vaccine product • Participating in IQ, OQ, and PQ equipment and purchasing chemical • Document control for the QC department • Writing and reviewing regulations, WI, SOP, and Specifications • Making monthly plans and reporting directly to the director

•Responsible for the analysis of packing materials, in-process materials, finished products, stability test samples using HPLC, AAS, UV-Vis, Karl Fisher Titrino. • Validation analytical methods and prepare the reagent and standardize volumetric solution. • Release/ reject incoming materials in SAP system for Plant • Review, revise the specification of incoming materials following the latest effective Pharmacopeia. •Control quality of raw materials in other sites

- Research and synthesize new cancer drug compounds - Equipment and chemicals management - Research and develop new pharmaceutical synthesis methods

• Implement test methods to control the quality of materials and feed products using QC tools • Document Control Coordinator of the lab by maintaining documentation and updating new SOPs • Be an internal auditor for integrated Audit Programs ISO 17025, ISO 9001:2015