Acting as front office for all documents submitted to CAPA or NODCAR.
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 getting Release permeation for any Shipment from CAPA.
Job Requirements
Medical background degree or equivalent professional qualification
At least 1-4 years relevant experience within the regulatory affairs discipline
CTD and Export Experience is preferable
Relevant product and industry knowledge is preferable
Pesticides and disinfectant Regulatory requirements
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