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Developed and implemented analysis of biological fluids for drugs and their metabolites following the current Good Laboratory Practices (GLP) guidelines of the FDA. Assays were developed using solid phase extraction (SPE), liquid-liquid extraction or protein precipitation and employing HPLC or UPLC with UV, fluorescence, and mass spectrometry detection systems to quantitate the analytes. Validated and maintained Analyst software used to control and acquire data from approximately 18 mass spectrometers. Supervised analyst in the automation group, which oversaw the operation, training, and maintenance of the Hamilton Star and Tomtec Quadra robotic platforms in the lab. Wrote and maintained the SOPs used in the operation and maintenance of the above equipment. Evaluated and recommended new equipment and software to be used in the lab. Wrote validation protocols and conducted the validation new instruments and any software used to control the instruments. Additional responsibilities included client interface, proposal writing, scheduling research associates' work and instrument time, validations, sample analysis, data review/interpretation, report preparation and invoicing.Specialties: GLP bioanalytical analysis, FDA audits, software validation, maintaining and programming liquid handling robots, LC/MS/MS
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Laboratory ManagerDshs - Central Office Feb 2024 - PresentUsNew Born Screening Mass Spec Lab -
Director Of Laboratory OperationsGenotox Laboratories Dec 2022 - Feb 2024Austin, Texas, Us -
Toxicology Lab ManagerGenotox Laboratories Apr 2015 - Dec 2023Austin, Texas, UsI currently manage the Toxicology Lab of Genotox Laboratories. We quantify pain management drugs in urine samples utilizing LC-MS/MS.
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ChemistDshs - Central Office Oct 2009 - Mar 2015UsI work in the Chemical Threat Lab. This lab's primmary task is running methods following CLIA regulations that were developed by the CDC. These methods measure human exposure to chemical weapons. My primary responsibility is the LC-MS/MS in the lab and the methods that are run on it.
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Senior Staff ScientistCedra Corporation Jan 2007 - Jun 2009Prepared and presented presentations on the company's position on current regulations.Interacted with clients in discussions about experimental design and trouble shooting methods.Evaluated and recommended new equipment and software to be used in the lab, such as Acquity UPLC systems and electronic laboratory notebook software. Developed LC/MS/MS methods for drugs and their metabolites from biological fluids following the current Good Laboratory Practices (GLP) guidelines of the FDA.Employed solid phase extraction (SPE), liquid-liquid extraction or protein precipitation sample preparation.Conducted analysis with HPLC or UPLC and quantitated by means of mass spectrometry detection. Authored and executed Validation Protocols (IQ/OQ/PQ) for new instruments and any software used to control the instruments following FDA 21 CFR part 11 guidelines.Wrote and maintained the SOPs used in the operation and maintenance laboratory equipment. Conducted sample data review and interpretation, investigations into unexpected results and report preparation.
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Automation Group LeaderCedra Corporation Oct 2006 - Jun 2009Supervised four analysts in the automation group and oversaw the operation, training, and maintenance of the robotic platforms in the lab; four Hamilton Stars, three Packard Multiprobes and four Tomtec Quadras. Provided leadership and managed the employee hiring process for the groupEvaluated employees and implemented disciplinary action as needed.
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Senior ScientistCedra Corporation Jan 2000 - Jan 2005Developed LC/MS/MS methods for drugs and their metabolites from biological fluids following the current Good Laboratory Practices (GLP) guidelines of the FDA.Employed solid phase extraction (SPE), liquid-liquid extraction or protein precipitation sample preparation.Conducted analysis with HPLC and quantitated by means of mass spectrometry detection. Presented posters on lab work at scientific meetings.Wrote and maintained the SOPs used in the operation and maintenance laboratory equipment. Authored and executed Validation Protocols (IQ/OQ/PQ) for new instruments and any software used to control the instruments following FDA 21 CFR part 11 guidelines, including Analyst software used to control Sciex mass spectrometers.
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Research AssociateMcw 1992 - 2000Worked on the isolation and identification using GC/MS of arachondonic acid metabolites. Synthesized radiolabeled compounds and various analogs.
Bill Edgemond Skills
Bill Edgemond Education Details
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Texas Tech UniversityOrganic Chemistry -
Ut Southwestern Medical Center
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Texas Lutheran UniversityChemistry
Frequently Asked Questions about Bill Edgemond
What company does Bill Edgemond work for?
Bill Edgemond works for Dshs - Central Office
What is Bill Edgemond's role at the current company?
Bill Edgemond's current role is Lab Manager.
What is Bill Edgemond's email address?
Bill Edgemond's email address is dr****@****bal.net
What is Bill Edgemond's direct phone number?
Bill Edgemond's direct phone number is +151297*****
What schools did Bill Edgemond attend?
Bill Edgemond attended Texas Tech University, Ut Southwestern Medical Center, Texas Lutheran University.
What skills is Bill Edgemond known for?
Bill Edgemond has skills like Glp, Hplc, Lc Ms, Mass Spectrometry, Validation, Analytical Chemistry, Method Development, Fda, Chromatography, Sop, Life Sciences, Lifesciences.
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