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Indianapolis, IN
June 09, 2018

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Eboni C. Gilbert

**** ***** *** ***. * Indianapolis, Indiana 46221

Cell: 317-***-****


Comprehension of GLP and cGMP standards.

Troubleshooting/root-cause analysis pertaining to quality and consistency of pharmaceutical drugs.

Operational knowledge of analytical instrumentation like HPLC, UV-Vis, AA, FT-IR, Karl Fisher (Volumetric/Coulometric), Dissolution equipment and data stations required.

Wet chemistry techniques include: Titrations, pH, Conductivity, and Heavy Metals analysis.

Interpretation and documentation of data, calculations and observations required.

Ability to execute multiple responsibilities, set priorities, clearly communicate ideas to others and respond positively to demanding situations.

Strong team player with attention to detail and desire to learn new things.

Familiar with Microsoft Software (Word and Excel), Chromatographic Software (Empower 2) and Spectroscopy Software (Win lab).



Chemist Saint Louis, MO May 2011 to January 2013

Compendial and non-compendial testing of raw materials per US Pharmacopeia- National Formulary

(USP-NF), European Pharmacopeia (Ph. Eur.) and American Chemical Society (ACS).

Timely analysis of in-process, release and stability products per customer request.

Create and revise sample lists specific to product specifications.

Order reagents and supplies pertaining to pharmacopeia monographs and operating procedures.

COVIDIEN Hazelwood, MO May 2010 to October 2010

Quality Control Analyst (Contract Position)

Perform chemical, physical and/or instrumental assay on in-process material.

Conduct weekly water and microbiological testing.

Prepare reagent mixtures and standards used in daily/weekly analysis.

Participate in laboratory maintenance such as instrument calibrations and waste management.

Analyze chromatography using Total Chrom and report official data into SIMS data base.

QUALITEST PHARMACEUTICALS Huntsville, AL October 2005 to July 2009

Research & Development Chemist

Conduct experiment al analysis on existing product formulations as well as new product development.

Participate in investigations for Out Of Specification (OOS) and Out Of Trend (OOT) test results.

OJT coordinator for new hires. Applications include: knowledge of various instruments, Standard Operating Procedures (SOP) and analytical methodologies.

Adhere to strict guidelines regarding the proficiency of notebook documentation.

Quality Control Chemist Huntsville, AL June 2005 to October 2005

Perform routine assay analysis on stability products as per USP 28 Chapter <621>.

Drug absorption analysis using dissolution techniques.

Physical characterization of pharmaceutical drugs by loss on drying, hardness and disintegration analysis.

Preparation of media and mobile phase by assigned concentration.


Alabama Agricultural & Mechanical University Normal, AL May 2005

B.S. Biology

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