Bio

I am an analytical chemist with 15+ years of experience working exclusively in a cGMP environment with a wide range of pharmaceutical products. My main area of expertise, and the focus of my career the past eight years, has been the evaluation of drug – packaging/delivery system compatibility for developmental pharmaceutical products. In this area I work extensively with mass spectrometry, both GC/MS and LC/MS, for qualitative identification of unknown substances as well as trace level quantitative analysis. Additionally, I have had extensive experience with the development of chromatographic and mass spectrometric methods, validation of these methods by IHC guidelines and execution of sample analysis throughout my career.