Testimonials for Gloria A. Rood
As President of Upsher-Smith Laboratories I worked with Gloria Rood for 5 years. During that period I observed her work product on a regular basis. Gloria’s work was always of the highest quality whether she worked as a team leader, a team member or while working with outside contractors. During our time together I found Gloria to be diligent, collegial and very consciencious. She works well with minimal oversight and writes first class scientific reports.
Given the opportunity I would not hesitate to hire Gloria in any capacity involving formulation, process development and/or scientific writing. Written: March 3, 2011
Ian Troup, President and COO, Upsher-Smith Laboratories
managed Gloria indirectly at Upsher-Smith Laboratories
I worked closely with Gloria during her time at Upsher-Smith as Sr. Pharmaceutical Development Scientist. Gloria represented the R&D arm of a customer for several product launches. Aggressive timelines were the norm for the product launches and it was extremely helpful to have such a knowledgeable and dedicated team member to help drive to the finish line. Gloria went beyond her role as R&D Scientist on the project team, supporting not only formulation development, scale-up and commercialization but also analytical and validation activities. I would recommend Gloria for any job or endeavor. Written: February 25, 2011
Commercial Client – Director, Technology Transfer
International Contract Manufacturing Organization
Gloria is a talented formulation development scientist, able to troubleshoot issues that inevitably seem to arise during the product realization process. She is highly skilled at remote management of difficult formulation scale-up, validation and full-scale production of pharmaceutical products and works successfully with individuals from a variety of backgrounds and skill sets. Gloria is a dedicated team member, able to take a project to completion, with a careful eye to timing and budgets. She frequently shared her knowledge through formal presentations and acting as an informal resource for staff across multiple departments. She effectively communicates complex topics to a wide audience. Written: March 2, 2011
Nancy Cameron, MS, ASQ CQA; Senior Regulatory Affairs Specialist
Midwest Medical Device Manufacturer
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