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Debra L. Jones
Regulatory Affairs
Debra Jones is a highly qualified professional with a Drug Development Certificate from Temple University School of Pharmacy.
She holds a Master of Science in Quality Assurance and Regulatory Affairs from Temple University School of Pharmacy, a Master of Business Administration in Business Administration and Management from the University of Phoenix, and a Bachelor of Arts in Biology from Rutgers University.
With an impressive background, Debra has held various positions in renowned pharmaceutical organizations such as Merck, Johnson & Johnson, Novo Nordisk A/S, GlaxoSmithKline, and more.
Her roles have ranged from Regulatory Affairs Manager to Study Director, Technical Writer, Scientist, Specialist, Associate Research Scientist, and Chemist, showcasing her diverse skill set and expertise.
Debra is a seasoned professional with a wealth of experience in regulatory affairs, stability studies, drug development, technical writing, and analytical chemistry, making her a valuable asset in the pharmaceutical industry.
