James L. Vesper designs
and develops instructional courses and workshops for the pharmaceutical
and medical device industries. He established and is president
of the firm LearningPlus, Inc. and has had more than 24 years
experience in the pharmaceutical industry.
Mr. Vesper worked eleven years at Eli Lilly
and Company,
Indianapolis, Indiana. His first assignment was as corporate industrial hygienist,
followed by three years in Corporate Quality Assurance. There, he was responsible
for issues concerning the manufacture and testing of parenteral products made
at Eli Lilly facilities and third parties worldwide. His last assignment was as
Project Leader of GMP (Good Manufacturing Practice) Education and Instruction,
establishing the department and its mission.
Since 1991, Mr. Vesper has been creating
innovative instructional training products for the pharmaceutical and health-care
industries using video and computer technologies as more effective
and efficient delivery media. Working as consultants with a wide
variety of clients, his firm creates integrated curricula for personnel
and customized training courses targeted to specific needs. He
presents papers and workshops at various international technical
and professional meetings, including those of the International
Society for Pharmaceutical Engineering (ISPE), GMP
TEA, PDA, Pharmaceutical
Sciences Group, and PharmTech.
In 1998 he presented at PDA, PharmTech Puerto Rico, and WORLDPHARM
conferences, as well as conducted courses for the Canadian
PSG in Toronto, Vancouver, and Montreal. In 1999 he joined
the faculty of the PDA Training and Research Institute, teaching
at a variety of locations in North American and Europe. In 2001,
he was awarded the PDA's Agallaco
Award for Excellence in Training.
With Learnwright,
Inc. of Rockville, MD, Mr. Vesper is co-developed a series
of web-based training programs covering basic, intermediate,
and advanced GMP, GCP, and other FDA/industry-critical topics. Mr. Vesper was executive producer
of pharma courses for Learnwright.
As an author, Mr. Vesper has written three
books published by CRC Press (formerly Interpharm Press):
Mr. Vesper has authored two additional books that are co-published by PDA and DavisHorwood
Publications.
Mr. Vesper is a contributing author for several publications, including: one chapter in Quality in Pharmaceutical Manufacturing (2004), edited by Richard Prince; four chapters
to Automation
and Validation of Information in Pharmaceutical Processing (1998) edited by Marcel Dekker; and, contributed to the WHO's World Health Organization GMP Requirements Part 3: Guide for Training (2006). A series of articles on training and
performance topics have been published in BioPharm in 2001 and
2002.
In addition to traveling extensively and
working on-site in Singapore, Latin America, India, France, England,
Ireland, Germany, Italy, and Puerto Rico, Mr. Vesper has been on
the faculty of Indiana University, teaching courses in Industrial
Hygiene and guest lecturing at other universities including the
University of Rochester. He has appeared on stage in the Metropolitan
Opera's production of Aida at New York's Lincoln Center in a supernumerary
role.
Mr. Vesper earned a B.S. in Biology from
Wheaton (Illinois) College and a Masters of Public Health from
the University of Michigan School of Public Health in Ann Arbor.
He is a member of the American Society for Training and Development
(ASTD), PDA,
Pharmaceutical Sciences Group (PSG),
and the Drug Information Association (DIA).
Mr. Vesper also serves on the Advisory
Board of BioInsights.
Since 1991, LearningPlus has worked with
clients in the North America, Europe, and Asia. Please see also
our list of clients using
LearningPlus services
and instructional programs. |