Scientist Ii Business Growth
Resume:
Cherry Li
Albany, CA *****
Cell 201-***-****
**********@*****.***
CAREER OBJECTIVE Seeking remote opportunities across industries, leveraging my expertise to support business growth and operational efficiency.
PROFESSIONAL STRENGTH:
Analytical scientist with more than 15 years of experience in the pharmaceutical analysis of APIs and drug products including solid, capsule, liquid, oral thin film and transdermal patch dosage forms
Hands-on expertise in HPLC, UHPLC, GC, UV/VIS, IR, Dissolution, Malvern Mastersizer, Multidose Dissolution and Fiber Optics dissolution, etc.
Extensive background in reviewing analytical data, laboratory investigations and stability program
Analytical method development and analysis using GC and HPLC
Effective oral and written communication skills, with strong team building abilities
High productivity, efficiency and accuracy
Familiar with cGMP and ICH guidelines
Expertise in Empower, HP ChemStation, Totalchrom, SAP, QDCS and LIMS
PROFESSIONAL EXPERIENCE
LTS-Lohmann Therapy Systems, West Caldwell, NJ 2013 to 2016
Scientist II
Collaborate with the Formulation Development Scientists to perform analytical testing in support of new formulation
Provide analytical support to technical transfer for scale-up and process optimization
Perform analytical method development with principle scientist
Perform method optimization
Prepare and execute method validation protocols and write corresponding reports
Analytical project lead for method transfer; lead cross function meetings involving technical transfer and client
Perform method transfer
Review analytical data and metrology calibration protocols and reports
Revise and review SOPs
Sandoz US Development Center, East Hanover, NJ 2009 to 2013
Scientist II
Provide timely, accurate analysis support for product development
Perform GC method development. Key scientist responsible for performing GC method development and analysis for all ARD projects.
Perform LC analytical method development
Perform method transfer
Prepare and execute method validation protocols and write corresponding reports
Review analytical data and final reports in compliance with SOPs and test methods
Revise SOPs
Pfizer (legacy Wyeth) through Kelly Scientific Services, Pearl River, NY 2009 to 2009
Scientist
Provide timely, accurate analysis support for API process development, optimization and manufacturing
Perform method development and method transfer
Review laboratory notebooks
PF Labs, Totowa, NJ 2003 to 2009
Scientist II
Perform analytical method optimization and method verification
Perform method validation; write protocols and corresponding reports
Initiate and complete Lab investigation reports
Review analytical data, validation protocols and final reports in compliance with SOPs and test methods
Review metrology calibration reports
Initiate and manage stability studies and create stability protocols in LIMS
Prepare stability reports
Revise SOPs
Introduce new technologies and analytical methodologies from R&D to QC laboratory.
Participate in special projects such as Empower and LIMS system update
Bristol-Myers Squibb Company, Garden City, NY 1998 to 2003
(Formally Dupont Pharmaceuticals Company)
Scientist
Perform analysis for finished products and stability samples
Perform method transfer, process validation and cleaning validation
Write investigation reports
Audit notebooks and reports
Train junior chemists
As LIMS super-user train and assist other chemists with electronic data input
Konica Imaging USA, Glen Cove, NY 1995 to 1998
Chemist
Perform analysis of raw materials and finished products
Develop analytical procedures
Lederle Laboratories through Lab support, Pearl River, NY 1995 to 1995
Analytical Chemist
Perform analysis for in-process samples
Education M.S. in Chemical Engineering,
City College, City University of New York
B.S. in Analytical Chemistry,
Guangdong University of Technology
Languages
Cantonese: Native / Fluent
Mandarin: Native / Fluent
English: Professional proficiency
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