An NSF International Company Mr James F Quebbeman
B.S. Cellular Biology, M.S. Physiology, M.A. Microbiology
- [email protected]
- + 1 857 277 0060
Jim’s background includes R&D, and clinical trial materials and marketed product manufacturing of traditional pharmaceuticals and biotech products. He has worked in the pharmaceutical industry for 25 years, after spending 10 years in academic and clinical research. He worked as a pharmaceutical consultant for R&D, medical device, biotech and pharmaceutical operations, with an emphasis on parenteral manufacturing, and worked in Quality Assurance for Warner-Lambert/Parke-Davis, Pharmacia, and Pfizer with compliance responsibilities for in-house activities as well as contract manufacturing of drug products. His experience includes facility design, renovation, and qualification as well as laboratory and manufacturing operations. He recently returned to pharmaceutical consulting, working with large and small companies worldwide to support their Quality and Compliance activities for the manufacture of API and drug products.
Areas of focus include aseptic processing and parenteral manufacturing, environmental monitoring, pharmaceutical microbiology, and Quality System development and management. He has co-authored numerous research publications, developed and presented training seminars, and presented at numerous professional organizations and meetings.
