Regulatory Affairs Professional
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I have worked in the biotech industry for over 15 years in diagnostics and pharmaceuticals. I have over three years of experience in regulatory affairs and have been highly involved with chemistry, manufacturing, and controls documentation and submissions to the FDA. I have authored and compiled Module 3 sections of regulatory submissions.
-Biotech industry for 15 years
-12 years was assay development scientist and 3 years regulatory affairs
I have a Ph.D. from University of Southern California in Biochemistry and Molecular Biology
