Almost twelve years of experience in Analytical R&D of a fast-paced cGMP pharmaceutical company. Specializing in both performing all various raw material tests listed in USP/NF, BP, EP and in developing, verification and/or validation of in-house methods (SOPs) based on USP/NF, EP, BP, or supplier's technical packages. Self-motivated and able to work independently. I always deliver accurate results for all my work followed both cGMP and cGDP procedures either on time or ahead of scheduled time.

Highlights:

• High Performance Liquid Chromatography (HPLC)
• QA/QC
• Test
• Distribution
• DSC
• EP
• Microsoft Excel
• Microsoft Outlook
• Microsoft Windows
• Microsoft Windows CE