LEON MCWILLIAMS CURRICULUM VITAE
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CONTACT INFORMATION
Pearland, Texas 77584
Cell Phone: 312-***-****
Email Address: ******************@*****.***
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EDUCATION
Graduate Degree: Master of Science
Molecular Biology, Microbiology, and Biochemistry (MBMB),
Southern Illinois University - School of Medicine, 2009
Undergraduate Degree: Bachelor of Arts
Biochemistry and Sociology, North Central College, 2000
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SCIENTIFIC INSTRUMENT & METHODS EXPERIENCE
High Performance Liquid Chromatography (HPLC)
Gas Chromatography (GC)
Gas Chromatography-Mass Spectroscopy Instrument (GC-MS)
Liquid Chromatography/Mass Spectroscopy (LC/MS)
Inductively Coupled Plasma/ Mass Spectroscopy (ICP/MS)
Automated Microparticle Processing System (AMPS)
Laboratory Information Management System (LIMS)
Electronic Laboratory Notebook (ELN)
Proper Protective Equipment (P.P.E.)
UV/VIS Spectrophotometer
ELISA
Karl Fischer Titrators
Turbidimeter
Gel Electrophoresis
Automated 96-well pipettor
Automated ELISA Plate Reader
Dynamic Light Scattering Instrument
Windows XP, Microsoft Word, PowerPoint, Excel, Access, Internet
Explorer, Netscape
GC/MS/MS
Thin Layer Chromatography
IR Spectrophotometer
NMR
EMPLOYMENT HISTORY
March 2014-Present Kelly Scientific Assignment
Lead Analytical Chemist
A member of an interdisciplinary team to aid AMPAC Fine Chemicals with
expansion to a previously vacated plant site in LaPorte, Texas. I am
responsible for re-establishing the laboratory under cGMP and cGLP
guidelines. My work also includes the re-certification of instrumentation,
work hoods, repairing Millipore water system, and the transfer of methods
and Quality system to the site. Lastly, I am responsible for the analyses
of all samples.
September 2011-January 2014 E. I. du Pont de Nemours and Company
Gregory, TX
QA Coordinator/ Plant Chemist
Responsible for the supervision of the Quality Control laboratory and
Quality Program for the DuPont Corpus Christi Plant site. Also I am
responsible for overseeing the Quality Program of other sites that are a
part of our business division. I am responsible for the process chemistry
for the site. This includes the making of 152a, which application includes
usage in aerosol cans. The production of 152a requires gas treatment, the
removal of impurities such as H2S.
. Direct all quality audits for the site and managed Internal
Quality Audit System for the site.
. Managed site's CAPA system concerning all Quality Incidents.
. Ensure the site is in compliance with ISO-9001, ISO-14001, and
FDA regulations.
. Responsible for answering customer complaints concerning quality
and generating responses for complaints towards suppliers.
. Serve as Management's representation for all issues relating to
quality.
. Lead all quality reviews for the site.
. Supervise a staff of 9 technicians for the complete data
analyses of the processes on the site.
. Assist technicians in the upkeep of instrumentation in our
laboratories.
. Responsible for the purchasing of instrumentation for the
laboratories.
. Lead all validations of laboratory equipment.
. As the site's Process Chemist, I gained invaluable PSM
experience with one of the world's safest companies.
. Responsible for leading all method development and modifications
for instrumentation and wet chemistry testing.
. Involved in the monitoring and changes to process chemistry for
the different areas of our plant.
. Support all testing for 152a including GC-PFPD analysis to
ensure sufficient gas treatment, the removal of H2S and other
sulfur containing compounds, has taken place.
. Lead for various 134A pharmaceutical batch campaigns.
. Accountable for the training and coaching of all technicians.
. Provide leadership for various projects on site concerning
analytical, quality, and community service.
. Site contact for all R&D projects.
. Six-Sigma Green Belt Certified.
. Provide technical assistance to customers.
Chicago, IL
March-September 2011 Blachford Corp.
Senior QC Technologist Responsible for the Quality Control testing on
lubricants produced by the company for our wire-producing clients (ferrous
and non-ferrous). Also acted as the R&D designate for the plant with the
company's main headquarters.
September 2006 - July City of Chicago-Water Chicago, L
2009 Department
Water Chemist II :
Responsible for performing standard analytical tests on water samples
from source water, filtration plants, distribution systems, and high
pressure boilers within the plant and to detect and determine if
various factors meet regulations set by Environmental Protection
Agency (EPA) and Illinois Department of Public Health (IDPH). Used ICP-
MS and chemical testing strips for analysis of various water samples.
. Led maintenance and calibration of laboratory instrumentation.
. Participated in tours of the facilities.
. Conducted performance testing to ensure compliance with EPA
regulation and perform periodic overview of analytical methods.
. Assisted in data quality review and periodic monitoring reports
to EPA and IDPH.
. Responsible for managing several projects simultaneously according
to management demands.
. Trained other scientists and engineers.
March 2005 - September U.S. Drug Testing Des Plaines, IL
2006 Laboratories
GC/MS Chemist:
Company is an independent contractor that analyzes various samples
from mothers and children that are high-risk for exposure to illegal
drugs.
. Primarily responsible for the operation, maintenance, and data
analysis of GC/MS,
HPLC, GC/MS/MS, and LC/MS instrumentation.
. Aided in the screening and confirmation of samples for possible
traces of various drugs
. Managed and maintained chain-of-custody documentation and records,
filing of the
results, and processing the samples for analysis.
. Method development, validation, and modification according to
customers'
Requirements.
. Trained technicians on instrumentation and served a supervisor role
during times lab
supervisor is absent.
Jan 2003- March 2005 Abbott Laboratories Abbott Park, IL
Chemist II (Contractor) :
. A part of a team that successfully developed and prepared Automated
Microparticle
Processing System Second Generation (AMPS2G) for production sectors
(customers).
. Calibration and operated AMPS2G. It processed polymer
microparticles with protein
coating for diagnostic kits.
. Designed and performed various practice runs with instrumentation to
mimic actual
formulation runs for production purposes.
. Method Development and Validation for AMPS II. Worked on writing
SOPs.
. Worked on investigations of probable causes of faulty formulation
production runs
using various instrumentation including HPLC.
. Qualified clean rooms for manufacturing purposes.
. Participated in API formulation runs. We produced detection kits for
various cancer
markers, HIV, etc.
. Trained under OPs and SOPs and entered data into LIMS system.
. Participated in maintaining and documenting our own lab's cGMPs and
cGLPs to ensure
FDA compliance was met.