Description
I am currently employed at a major pharmaceutical company in the Denver Area. Here I have worked as a tableting technician on the production floor, in the microbiology laboratory for three years, as a Production Facilitator specializing in document management, and finally am presently transitioning into stability software LIMS development for the past six months. I have experience assisting audits for FDA, DEA, and other regulatory agencies as a Document Management Lead, Scribe, Tour subject matter expert, etc. I have nearly five years previous background as a chemist (Hutchinson Technology, Hydrite) and in biotech research (Monsanto). I would be excited to utilize my well-rounded skill set!
