Regulatory Affairs Specialist

Job Description

• 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