Ming Liu
About Ming Liu
Ming Liu is a Manager/Scientist at Bristol Myers Squibb with extensive experience in analytical sciences and pharmaceutical research.
Current Role at Bristol Myers Squibb
Ming Liu currently serves as a Manager/Scientist at Bristol Myers Squibb in New Brunswick, New Jersey, United States. In this role, Liu actively participates in cross-functional teams as the analytical subject matter expert (SME), representing the interests of Technical Operations. Liu's responsibilities also include assisting QC sites and CMOs with out-of-specification (OOS) and out-of-trend (OOT) investigations and troubleshooting.
Previous Experience at Purdue Pharma L.P.
From 2011 to 2017, Ming Liu worked as a Senior Scientist in Analytical Sciences at Purdue Pharma L.P. in Cranbury, New Jersey. Over six years, Liu's role involved conducting various types of analytical testing and method validations as part of the Analytical Sciences team. The position demanded expertise in high-performance liquid chromatography (HPLC) and dissolution method development.
Tenure at Pfizer
Ming Liu has accumulated significant experience working at Pfizer in different capacities. From 2002 to 2010, Liu was a Research Scientist in the Chemical & Screening Sciences department in Princeton, NJ. Before this, from 1996 to 2001, Liu served as a Research Scientist in the Department of Pharmaceutical Sciences in Pearl River, NY. These roles involved preformulation developability studies, analytical problem-solving, and method validation.
Educational Background
Ming Liu holds a Master's degree in Analytical Chemistry from The University of Texas at Austin, completed between 1990 and 1994. Previously, Liu earned a Bachelor of Science in Pharmacy from Beijing Medical University, completed from 1983 to 1988. This educational foundation has facilitated Liu's extensive career in analytical and pharmaceutical sciences.
Specialized Skills and Methodologies
Throughout the roles held at various companies, Ming Liu has developed specialization in HPLC and dissolution method development, validation, and GMP sample testing. Liu utilizes current software tools for managing data, analyzing results, and generating reports. Additionally, Liu performs periodic method reviews, reviews change control documents, and supports regulatory filings, always ensuring that experiments comply with current Good Manufacturing Practices (cGMP) and internal Standard Operating Procedures (SOPs).