Position :-Regulatory Affairs -ROW Market (Formulation)
Roles & Responsibilities :
Preparation, Compilation and Review of dossiers in CTD/country specific format for ASIA or LATAM or AFRICA or MENA & CIS Regions.
Co-ordinating with cross functional departments like API, R&D, QC, QA, PDD, Micro for documents required for dossier compilation for initial submission, query responses or other submission like tender activities.
Manufacturing Site GMP Inspection supports with Customers & Cross Functional Departments.
Communicating with agents/partners for submission of Dossiers and further updates or requirements if any on product registration.
Participating in calls with agents/partners for submission of Dossiers and further updates or requirements if any on product registration.
Responding to queries with in the time lines received from client/agency. ...
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