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Director,
Intercontinental Regulatory Affairs

Responsible for strategizing product regulatory submissions to meet Marketing and
Intercontinental health agency requirements
and the Division worldwide business goals.
Requires knowledge of U.S. and Intercontinental regulatory requirements and registration
procedures. Will interpret FDA guidelines,
Code of Federal Regulations (CFR) and their
impact on Intercontinental registrations. Will
support Regulatory Affairs in international
expansion activities for non-U.S., non-Euro geographies including Mid-East, Far East,
Asia, Africa, Japan. 25-30% travel

Requirements: BS or MS relevant to
Regulatory Affairs: biological sciences,
pharmacy, or medical discipline. Minimum
5 years in pharmacy or biotechnology
Regulatory affairs. Experience with foreign
regulatory affairs is preferred.