I am an experienced analytical scientist with emphasis on method development and validation, particularly for Residual Solvents by GC/FID and Assay/Impurity analysis by HPLC/UHPLC, with experience in both the pharmaceutical and environmental industries. Most recently, I have gained valuable experience and insight into project management/project coordination by managing business critical product transfers as part of a small, specifically selected, high performing team. I have proven to be successful at communicating progress, as well as challenges, along with a plan for completion to a successful outcome that meets the needs of all involved. Excellent at protocol and report writing. My performance demonstrates the ability to judiciously approach a project with a sense of urgency and clarity to get to a successful outcome, whether that is in method development, validation, or management of method transfers. My approach has consistently been laser-focused with quality and attention to detail, while being flexible to changing priorities and deadlines.