In this role, you will be responsible for advising Distribution Center management and designated staff on the actions necessary to maintain compliance with quality and regulatory standards, including the ISO 9000 international standard
In this role, you will be responsible for
the preparation, organization, and management of submissions to the US FDA for clinical stage molecules being developed in the lab for the prevention and/or treatment of HIV infection.
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$45K to $75K -Tarrytown, NY
This position prepares regulatory submissions for in vitro diagnostic products for international registrations. Focus will be on new product registration and re-registration of products in China. Must possess good technical writing skills and have a scientific background.