Dr. Jon S. Kauff man is Sr.
Director of Biochemistry,
Method Development &
Validation and Protocol
Development and Technical
Writing at Lancaster Laboratories. His teams
are responsible for developing and validating
methods and performing analysis of clinical and
commercial samples for stability and release
purposes. This includes methods for the testing
of residual impurities in biopharmaceutical
products and in-process samples.
Dr. Kauff man’s
departments also perform mass spectrometric
characterization and leachable and extractable
studies. Dr. Kauff man’s key roles are to interface
with clients and his team to ensure positive
project outcomes by maintaining compliance and
a high level of quality; meeting milestones and
delivery requirements; and finding cost-eff ective,
value-added solutions. He earned a doctorate in
chemistry from the University of Delaware and
has over 25 years of experience in the analytical
testing field.
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