Requires Master's in Pharmaceutics, Pharmacy, Chemistry or closely-related field & 3 yrs experience designing analytical experiments in the pharmaceutical and/or consumer products industry; applying HPLC, LC-MS, GC, UV-Vis, FT-IR and/or AAS to validation and/or stability studies for pharmaceuticals; performing method development & validation of pharmaceutical tests, including assay, impurities, and dissolution; evaluating & interpreting stability data; performing in-vitro release testing of topical and/or transdermal dosage forms; managing CMOs & CDMOs to deliver comprehensive and compliant analytical development, validation, and stability studies for drug substances and/or drug products; drafting responses to deficiencies from EMA, ROW, and/or FDA- IR letters; performing Accelerated Stability Assessment Program stability studies on drug products; drafting & closing OOT and OOS investigations, CAPA's and lab related deviations using Veeva. Staff Scientist, Analytical Development for Morristown, NJ to design analytical experiments for method development, method validation & method transfer to manufacturing sites; perform laboratory work; prepare product specifications; plan stability studies & interpret results; present findings regarding underlying chemistry of products in pipeline.