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C
Chemistry expert
Twelve years experience in US and Europe, gaining an understanding
of global regulatory requirements.
Directing chemical process Development and Validation, GMP
manufacturing activities, technology transfer, supervising
a process development laboratory.
M
Manufacturing expert
Six years of experience in leading pharmaceutical production
in EU and US plant. Experience in injectable (SVP, LVP,
solid and Lyophilized products) and solid oral dosage forms
for worldwide approved drugs.
Experience in development, technology transfer, validation
and manufacturing.
Experience in pharmaceutical project management.
C
Analytical expert
Six years experience in leading an analytical development
department with responsibilities in development, validation
and transfer of analytical methods.
Two years experience in pharmaceutical process validation.
Ten years experience in design and synthesis of potential
anticancer molecules.
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