Main Job Tasks and Responsibilities:
*Collect and coordinate information and prepare regulatory documentation for submission to regulatory agencies or to commercial partners
*Advise on the submission strategy Timely compile materials for license renewals, updates and registrations Maintain regulatory files/database and chronologies in good order.
*Establish and maintain system for tracking changes in documents submitted to agencies or partners Responsible for all steps of Research issues
*Responsible for following steps of formulations and stability study of any New
*Products. Responsible for execution of Damaged and Expired products
* Responsible for getting Release permeation for any Shipment from CAPA
*Responsible for following the Analysis Certificates from NODCAR

Job Requirements
Education and Experience:
*Medical background degree or equivalent professional qualification
*At least 3-2 years relevant experience within the regulatory affairs discipline
please send your CV with a recent Picture to the following email: hr@zeta-pharma.com