Ning Pan
** ***** ******, *****, ** *****
Home: 978-***-****
E-mail: ning,*******@*****.***
PROFILE
Analytical scientist with 14 years experience in pharmaceutical drug discovery and development.
Expertise in LC/MS data acquisition and analysis, HPLC and SFC achiral/chiral analysis as well as
purification.
EXPERIENCE
2000 – 2011
Pfizer/Wyeth, Cambridge, MA
I/I Chemistry/Discovery Analytical Sciences
Scientist (2009-2011)
Research Scientist II (2004-2009)
Research Scientist (2000-2004)
Provided analytical expertise to support Pfizer/Wyeth drug discovery function at Cambridge site in
following areas: 1) compound characterization by LC/MS, 2) purity determination by HPLC and SFC, 3)
milligram to gram scale purification by preparative HPLC, SFC, and automated preparative LC/MS
system, 4) supporting an open-access lab equipped with LC/MS, HPLC and preparative HPLC systems.
Performed LC/MS analysis daily with Waters LCT Premier and Agilent MSD to characterize final
compounds, synthetic intermediates as well as high throughput screening candidates. Contributed to
therapeutic research by developing and executing LC/MS methods to resolving project related
issues, such as determination of hydrolysis rate of pro-drug candidates in biological matrix.
Trained by Waters on Micromass LCT and Waters ZQ as well as Synapt G2 HDMS systems on
instrument operation, maintenance and problem troubleshooting.
Provided method development expertise in NP-HPLC, RP-HPLC, and SFC for achiral and chiral
analysis. Developed methods for purity and chiral purity determination of many challenging
compounds. Performed stability studies to support drug discovery projects. Summarized the results
and wrote the reports.
Have extensive method development experience in preparative purification. Purified compounds
with HPLC/MS for challenging compounds, such as compounds for toxicity studies, or degradation
products.
Trained and certified by Waters on operating Thar SFC/MS and Berger multi-gram preparative SFC
system. Developed and executed SFC methods for chiral purification of novel compounds to
support high priority projects.
After merger with Pfizer, implemented and operated Waters Auto Purification System to support
Immunology/Inflammation Chemistry on regular basis. This automated system allows direct scale
up from analytical testing to LC/MS based purification for batch process.
Supported an open-access analytical laboratory equipped with Waters LCT-Premier, Waters ZQ,
Agilent MSD, and Waters preparative HPLC systems. Developed and implemented new methods in
open access lab, performed routine instrument maintenance and problem solving, and provided
training to chemists.
Interacted with Medicinal Chemistry Department and Therapeutic Discovery Department very
closely for coordination of testing timelines and provided training to medicinal chemists on open
access systems.
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1998– 2000
Eli Lilly & Company, Indianapolis, IN
Biopharmaceutical Development
Analytical Chemist
Developed and validated separation-based analytical methods such as SEC, RP-HPLC, IE-HPLC,
and Peptide Mapping for release and stability testing of new biopharmaceutical compounds.
Performed product characterizations on reference standards, bulk drug substances, and formulated
drug products with SEC, RP-HPLC, IE-HPLC and other analytical technologies.
Established the stability testing procedures as well as method validation and transfer protocols,
summarized testing results and wrote technical reports on analytical method development, and
method validation.
Conducted accelerated stability studies and provided trend analysis for main peak and product-
related impurities.
Worked closely with formulation development groups and responsible for providing HPLC-based
analytical supports.
Familiar with ICH guidelines and cGMP regulations related to biopharmaceutical testing. Provided
scientific data for IND filings.
1996 – 1998
Fujisawa USA, Inc., Malrose Park, IL
Pharmaceutical Sciences
Associate Scientist
Developed and validated HPLC methods for drug substance and drug product release and stability
testing of small molecule candidates under cGMP environment.
Conducted stability studies for drug substance and drug product and provided trend analysis for active
ingredient and related impurities. Characterized reference standards and drug product with various
analytical technologies. Performed analytical method transfers between Analytical and QC labs.
Prepared technical protocols, reports, and analytical testing procedures. Prepared documents for FDA
submissions
Skilled in a variety of analytical techniques such as HPLC, IC, GC, FTIR, UV/VIS, and Karl Fisher.
Provided training for new lab scientists
Abbott Laboratories, North Chicago, IL 1994 - 1994
Corporate Industrial Hygiene
Lab Technician
Developed and validated sensitive HPLC methods for the determination of trace level
pharmaceutical compounds in aerosol in manufacturing facility.
Optimized separation conditions and improved detection sensitivity for HPLC methods.
1991 – 1993
University of Iowa, Iowa City, IA
Department of Chemistry
Teaching and Research Assistant
Conducted M.S. thesis research at Professor Donald J. Pietrzyk's research lab. Studied the retention
behavior of anionic surfactants on different polymer based anion exchangers.
Determined the parameters that affect the retention time, selectivity, and resolution of anionic
surfactants. Optimized the separation conditions for surfactant mixtures containing homolog and
positional isomers.
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Supervised undergraduate analytical laboratory
1984 – 1989
Northern Institute of Technology, Beijing, PRC
Department of Chemistry
Instructor
Instructed undergraduate courses of Analytical Chemistry and Instrumental Analysis
Supervised undergraduate analytical laboratory
EDUCATION
M.S. Analytical Chemistry University of Iowa
B.S. Chemistry Beijing Normal University
AWARDS
Chemical Screening Science Above and Beyond Award, Wyeth, 2004
Employment of the Month, Fujisawa USA
PUBLICATIONS
1. Xiang, Jason; Ipek, Manus; Suri, Vipin; Massefski, Walt; Pan, Ning; Ge, Ying; Tam, May; Xing,
Yuzhe; Tobin, James F.; Xu, Xin; Tam, Steve, “Synthesis and biological evaluation of
sulfonamidooxazoles and β-keto sulfones: selective inhibitors of 11β -hydroxysteroid dehydrogenase
type I”, Bioorganic & Medicinal Chemistry Letters 15(11), 2865-2869, 2005.
2. Ramarao, Manjunath K.; Murphy, Elizabeth A.; Shen, Marina W. H.; Wang, Yuren; Bushell, Kristen
N.; Huang, Nelson; Pan, Ning; Williams, Cara; Clark, James D., “A fluorescence-based assay for
fatty acid amide hydrolase compatible with high-throughput screening”, Analytical Biochemistry
343(1), 143-151, 2005.
3. Pan, N., Pietrzyk, D.J., “Retention of Anionic Surfactants on Anion Exchangers”, J. of
Chromatography. A, 706, 327-337, 1995.
PRESENTATIONS
1. Pan, Ning; Huang, Nelson; McConnell, Oliver; “LC/MS analysis of pharmaceuticals using
multimode ionization source”, Conference on Small Molecule Science, Chapel Hill, NC, July 2007.
2. Huang, Nelson; Bourassa, Jim; Ge, Ying; Pan,Ning; Xiang, Jason; Suri,Vipin; Zhang, Yan-Ling;
“LC/MS and LC/MS/MS Analyses for Screening and Characterization of 11b-Hydroxysteroid
Dehydrogenase Type I (11b-HSD1) Inhibitors”, ASMS, San Antonio, TX, June 2005.
3. Huang, Nelson; Massefski, Walt; Pan, Ning; McConnell, Oliver; “Evaluation of electrochemcial
oxidation as a tool for studying phase I metabolism and metabolic stability, Part II: Purification and
structural characterization of the oxidative products”, Conference on Small Molecule Science,
Bristol, RI, August 2005.
4. Huang, Nelson; Bourassa, Jim; Massefski, Walt; Pan, Ning; Wan, Anna; McConnell, Oliver;
“Evaluation of electrochemcial oxidation as a tool for phase I metabolism and metabolic s tability
studies”, Conference on Small Molecule Science, Bristol, RI, August 2004.
5. Pan, Ning; Lee, Jinbo; Kung, Leslie; Huang, Nelson; “HPLC stability analysis of drug candidates
from discovery research” 32nd Northeast Regional Meeting of the ACS, Rochester, NY,
October 2004.