Neal Merritt
Taylors, South Carolina 29687
Telephone: 864-***-****
E-Mail: **********@*******.***
Objective:
Seeking a position in the following area:
Analytical Chemistry / Compliance
PROFILE:
. Science-based background encompasses experience in the following areas
(Instruments/Methods): Gas Chromatography-Mass Spectrometer (GC-MS); UV-
Visible Absorption Spectrometer; Infrared Spectrometer; Atomic
Absorption Spectrometer; Column Chromatography; HPLC; GC
. Other experience includes: Preparing/maintaining job sites; ordering
supplies; coordinating deliveries; training; supervision; sales;
inventory control; computer use (Word; Excel; Outlook; PowerPoint;
Internet; E-Mail; SAP, RTPS, ChemStation, Empower).
. Strengths: Excellent interpersonal skills; ability to learn quickly;
analytical; proven supervisory and organizational abilities; strong time
management skills; excellent writing and leadership abilities; problem
solving;
EDUCATION:
. Bachelor of Science - Major in Chemistry (May 2006); The Citadel, The
Military College of South Carolina, Charleston, SC
. High School Diploma (2002); Eastside High School, Taylors, SC
SELECTED ACCOMPLISHMENTS:
. The Citadel's Dean's List; The Citadel Cadre Sergeant; Genco Lifeguard
of the Month (2 times); High School Varsity Letterman (4 times); S.C.
State Wrestling Team Champions; The Citadel Platoon Sergeant;
EXPERIENCE:
Quality Control Chemist I
BASF, Greenville, South Carolina September 2013
- November 2014 (contract)
. Perform raw material, in process, and finish product testing; operate
HPLC and GC (Chem Station), FTIR, MIR, NIR, Karl Fischer (volumetric
and coulometric), pH, and wet chemistry techniques such as hydroxyl
value, acid/amine value, and iodine value; communicate with production
concerning in-process testing to make batch adjustments, assist in
updating batch sheets and data sheets; maintain laboratory inventory.
Validation & Compliance Coordinator
Span Packaging Services, Greenville, South Carolina December
2012 - July 2013 (contract)
. Conduct validation or qualification tests of new or existing processes
and equipment in accordance with internal protocol or external
standards; prepare, maintain, or review validation and compliance
documentation; generate protocols, validations, and verifications for
new packaging processes, customers, and products; manage the change
control system; write IQ/OQ/PQ for new packaging equipment; compile and
review packaging batch records; collect and inspect retain samples on
customer products, and collect validation/verification samples; ISO
13485; 21 CFR Part 820; cGMP
Validation Specialist
Bausch + Lomb, Greenville, South Carolina March 2012
- November 2012 (contract)
. Conducted validation or qualification tests of new or existing
processes and equipment (lab, packaging, and sterilization) in
accordance with internal protocol or external standards; prepared,
maintained, or reviewed validation and compliance documentation such as
engineering change notices, or protocols; generated protocols for new
processes and equipment; wrote final reports; conducted yearly
reassessments on processes and equipment to identify gaps and remediate
them.
Analytical Chemist II
Irix Manufacturing, Inc., Greenville, South Carolina
2010-2012
. Performed raw material, in process, and finish product testing;
operated HPLC and GC (Chem Station), FTIR, Karl Fischer (volumetric and
coulometric), pH, melting point (DSC), particle size analyzer, TOC, and
wet chemistry techniques; communicated with production concerning in-
process testing; wrote investigation and deviation reports, change
controls, out of spec and preventative action reports to comply with
FDA regulations in a cGMP environment; HPLC operational re-
qualification and preventative maintenance.
Outside Sales Representative 2008-
2009
VLS Recovery Services LLC, Greenville, South Carolina / Fitzgerald,
Georgia
. Increased business with existing customer base; expanded business with
new customers in the need of industrial waste services; presented
company services to prospects; ensured accurate reporting and accounting
of sales leads assigned through proper use of daily recaps and ongoing
reporting; achieved individual sales targets.
Quality Control Chemist
2007-2008
Pharmaceutical Associates Inc., Greenville, South Carolina
. Performed assays on company products utilizing process control measures;
used UV/Vis, IR, AA, Karl Fischer, and density meter instrumentation;
maintained inventory of lab supplies; researched and implemented new
methods; cGMP/FDA regulations.
Metallographic Technician 2006-2007
Protech Lab Corp, Hilton Head, South Carolina
. Prepared samples for analyses by cutting, mounting, grinding, and
polishing, to reveal microstructural constituents of the coating;
performed tensile tests; ran corrosion test; calculated macro hardness
of coating for specimens; reviewed and recorded results for evaluation
reports; maintained laboratory inventory.
References Available Upon Request