Lisa Hernandez
**** ****** *** ***. * Phone: 573-***-****
Columbia, MO 65201 Cell: 618-***-****
Email: *******@*****.***
Career Focus
Motivated Analytical Chemist with over five years experience in the pharmaceutical industry and a strong ability to work independently or as a team member
Core Strengths
• Extensive experience with HPLC, UV/VIS, FTIR, Dissolution and wet chemistry techniques
• Excel in analyses of raw material, in-process, finished product, and stability samples using in-house and USP methods for solid dosage and liquid products
• Excellent maintenance of documentation following cGLP and cGMP regulations in accordance with FDA and DEA guidelines
• Quality problem-solving ability, attention to detail, and communication skills
Technical Skills
• Knowledge of instrument calibration
• Computer software: TotalChrom, LIMS, SAP, Empower, and Microsoft Office: Word, Excel, and Power Point
Employment History
ABC Laboratories, Inc- Columbia, MO 11/07/2011- Present
Associate Scientist
• Independently performs complex pharmaceutical experimentation and method validation using HPLC, Dissolution, TLC, and other wet chemistry techniques in compliance with cGMP regulations according to method, protocol, and standard operating procedures
• Performs standard and sample preparations for data analysis
• Performs and maintains instrument calibration
• Responsible for the quality and accuracy of data and reports sent to clients under assigned responsibility
Sigma-Aldrich/ Kelly Scientific- St. Louis, MO 06/2011-10/2011
Quality Control Chemist
• Method validation and Cleaning validation using HPLC, TOC, and surface sampling
• Raw material and solid dosage testing using wet chemistry techniques including pH, Appearance, FTIR, UV/VIS, and Karl Fisher
• Writing and revising SOPs
• Instrument calibration
KV Pharmaceutical- Earth City, MO 2006-2009
Chemist I
• Quality control analysis of in-process, stability, and finished products using HPLC, UV/VIS, Dissolution, FTIR, and wet chemistry techniques
• Conducted OOS investigations
• Responsible for writing and revising In-house methods and SOPs
• Maintained excellent documentation following cGLP and cGMP regulations
• Participated in laboratory housekeeping and maintenance; such as instrument calibrations
• Participated in 5S organization of the laboratory
PD George- St. Louis, MO 06/2006-12/2006
Analytical Chemist
• Quality control analysis of raw material, in-process, and finished product of polymers, lubricants, and other environmental samples using IR, GC, viscosity, and wet chemistry
• Record keeping of all incoming raw material samples
• Maintained data entry of laboratory results following GLP and cGMP regulations
Virbac/Aerotek- Bridgeton, MO 2004-2005
Analytical Chemist
• Quality control analysis of in-process, stability, and finished products using HPLC, UV/VIS, dissolution, and wet chemistry techniques
• Independently analyzed raw material samples using IR, UV/VIS, TLC, titrations, and viscosity
• Maintained excellent documentation following cGLP and cGMP regulations
• Participated in laboratory housekeeping and maintenance; such as instrument calibrations
Education
University of Missouri- St. Louis 2011
Bachelor of Science, Biology specializing in Genetics, Cell, and Molecular Biology
St. Louis Community College at Florissant Valley 2003
Associate of Applied Science, Chemical Technology