Review, prepare & compile CTD/ Dossiers for various dosage forms (tablets / capsules / granules / liquids) for submission to South African regulatory authorities.
Provide timely response to comments/ queries received from regulatory authorities.
From a reputed pharmaceutical company manufacturing dosage forms.
Well versed with preparation of dossiers & other documents for registration in SA.
Desired candidate profile:-
Edu : M.Pharma
Yrs of exp :6-10 yrs
Exp details : Should have experience in handling Regulatory Affairs for South Africa market for formulation.