Brian Talbot Email & Phone Number

Alachua, Florida

Alachua, FL

Develop and validate GMP methods for the quantification and characterization of various proprietary proteins and peptides using capillary electrophoresis, reverse phase, ion exchange, and size exclusion chromatography. Carry out method transfers of GMP methods between client laboratories and receiving laboratory. Prepare written reports for client.

Columbia, MO

Develop and validate GMP methods for the quantification and characterization of various proprietary proteins and peptides using capillary electrophoresis, reverse phase, ion exchange, and size exclusion chromatography. Carry out method transfers of GMP methods between client laboratories and receiving laboratory. Prepare written reports for client.

Rocky Mount, North Carolina Area

Analyzed intravenous formulations for both active drugs and excipcients using high performance chromatography. Performed method transfers, hold time and equipment cleaning studies for drug product reformulations and new drug products. Analyzed product complaints and product stabilities for potency and impurities.

Clayton, NC

Performed quantification and characterization of human insulin derived from yeast cells using reverse phase chromatography, size exclusion chromatography, and HPCE. Analyzed the various excipients used in the product formulation before and after formulation to ensure the products were properly formulated. GMP reviews the work of other analysts in the group.

Clayton, NC

Write documentation for the human immunoglobulin chromatography project. This documentation includes all standard operating procedures used in the manufacturing of human immunoglobulin.

Zebulon, NC

The goal of the project, Project Aladdin, was to bring all analytical methods in Glaxo Wellcome up to today’s current regulatory requirements, not only in the United States, but also everywhere in the world. The Project Aladdin process identified the methods for drug assay, process impurities/degradants, content uniformity, and dissolution that would.

Wilmington, NC

Developed and validated GMP methods for the quantification and characterization of various small molecules, proprietary proteins and peptides using capillary electrophoresis, reverse phase, ion exchange, and size exclusion chromatography. Carried out method transfers of GMP methods between client laboratories and receiving laboratory. Prepared written.

Sparks, MD

Designed, implemented and supervised experiments for the development of a Rapid Identification and Susceptibility System. Established and optimized biochemical enzymatic assays. Established and instituted quality control procedures to maintain optimum substrate conditions and stability. Developed assays for key components in media and the antibiotics.

Baltimore, Maryland Area

Responsible for the supervision and performance of the monthly production calendar. Scheduled the assays to be performed and established priorities. Prepared work schedules and assigned duties, supervised project leaders and laboratory technicians, assisted personnel with analytical problems and questions, trained new employees. Assumed responsibility for.

Edgewood APG, MD

Provided critical scientific suggestions in the preparation of protocols. Responsible for all phases of the research process, including problem definition, planning, execution, analysis and interpretation, and reporting of results in journals and at local and national scientific meetings. Developed assays and instrumented procedures using HPLC and GC for.

Bachelor'S Degree, Biology, General

Publications

Science