- Responsible for transferring formulations and producing generic or brand cGMP clinical products. - Produce pre-clinical supplies for research and analytical method studies and clinical supplies for IND studies from phase I to phase III and post-approval phase IV supplies.- Research and development product manufacturing activities for Transdermal systems including in-process controls and production documentation functions.- Mixing and laminating processes with various… Show more - Responsible for transferring formulations and producing generic or brand cGMP clinical products. - Produce pre-clinical supplies for research and analytical method studies and clinical supplies for IND studies from phase I to phase III and post-approval phase IV supplies.- Research and development product manufacturing activities for Transdermal systems including in-process controls and production documentation functions.- Mixing and laminating processes with various technologies- Familiar with requirements of DEA, FDA and other governing bodies in the pharmaceutical industry.-Department Training Coordinator-Watson Qualified Trainer since June 2008.-Enters Purchase Orders for Group Show less

Developed and tested a novel design for total knee replacement stability, specifically tibial implantation. Analysis of implant included Instron mechanical testing followed by Scanning Electron Microscope analysis.

Marketed Biological/Biomedical technologies developed at the Univ. of Utah to the commercial market. Developed and maintained database of client contact information. Prepared non-confidential summaries of patented technologies for licensing managers, performed patent searches, and market analysis