Myron Vance Email & Phone Number | • Perform development stability testing and non-GMP production testing • Maintain the laboratory in accordance with SOPs. • Operate and maintain analytical instrumentation for development testing, including routine preventive maintenance and troubleshooting. • Write, revise and review Standard Operating Procedures, Material Specifications, Forms, Protocols and Reports. • Familiar with advanced analytical techniques for HPLC, UV/Vis, FTIR, GC, and Nasal Spray Testing and executes tasks without supervision or under the direction of a test method, standard operating procedure, or a protocol. • Responsible for design and conduct of defined sets of experiments in support of a quality by design (QbD) process assisted by statistical design software • Understanding of cGMPs and develop understanding EMEA regulations • Excellent oral and written communication skills. • Recommend and implement innovative approaches to problem solving. • Utilize investigative skills for aberrant result laboratory investigations. • Mentor Development Scientist I and II levels Specialties HPLC by DAD & VWD Detection HPLC/MS ESI APCI GC/FID GC/TCD GC/ECD UV/VIS Osmometer IR Viscosity DSC TGA ICP AA Graphite Furnace AA Microwave Digester/Extractor Viscometer Stereo Microscope Liquid-Liquid Extractions ELISA techniques Gel electrophoresis GLP and GMP

Myron Vance

• Perform development stability testing and non-GMP production testing • Maintain the laboratory in...
Lexington, Kentucky, United States

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Myron Vance’s Location Lexington, Kentucky, United States

Myron Vance’s Current Industry Summit Biosciences

Myron Vance’s Prior Industry Murty Pharmaceuticals | State Medical Examiners Office | Envirodata | University Of Kentucky | Transduction Laboratories

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Development Operations Supervisor

2022-04-01 00:00:00 - Present

QC/R&D Chemical Analyst

2003-07-01 00:00:00 - 2012-08-01 00:00:00

Forensic Chemist II

2002-12-01 00:00:00 - 2003-06-01 00:00:00

Environmental Chemist/Analyst

2000-04-01 00:00:00 - 2002-12-01 00:00:00

Senior Laboratory Analyst

1999-01-01 00:00:00 - 2000-04-01 00:00:00

Laboratory Technician

1998-09-01 00:00:00 - 1999-01-01 00:00:00

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Myron Vance is a • Perform development stability testing and non-GMP production testing • Maintain the laboratory in accordance with SOPs. • Operate and maintain analytical instrumentation for development testing, including routine preventive maintenance and troubleshooting. • Write, revise and review Standard Operating Procedures, Material Specifications, Forms, Protocols and Reports. • Familiar with advanced analytical techniques for HPLC, UV/Vis, FTIR, GC, and Nasal Spray Testing and executes tasks without supervision or under the direction of a test method, standard operating procedure, or a protocol. • Responsible for design and conduct of defined sets of experiments in support of a quality by design (QbD) process assisted by statistical design software • Understanding of cGMPs and develop understanding EMEA regulations • Excellent oral and written communication skills. • Recommend and implement innovative approaches to problem solving. • Utilize investigative skills for aberrant result laboratory investigations. • Mentor Development Scientist I and II levels Specialties HPLC by DAD & VWD Detection HPLC/MS ESI APCI GC/FID GC/TCD GC/ECD UV/VIS Osmometer IR Viscosity DSC TGA ICP AA Graphite Furnace AA Microwave Digester/Extractor Viscometer Stereo Microscope Liquid-Liquid Extractions ELISA techniques Gel electrophoresis GLP and GMP

Myron Vance has prior
experience in the following industries:
Murty Pharmaceuticals | State Medical Examiners Office | Envirodata | University Of Kentucky | Transduction Laboratories

Myron Vance has the following professional experience:
Summit Biosciences | Murty Pharmaceuticals | State Medical Examiners Office | Envirodata | University Of Kentucky | Transduction Laboratories