Studying various legal documents circulated by Directorate General of Drug Administration (DGDA)Ensuring different type of drugs related activities and approval from DGDA.Performing various activities to get the drugs manufacturing license (New/Renew) from DGDA.Keeping up to date with changes in regulatory legislation and guidelines.Receiving packaging, annexure, price and marketing authorisation approval etc. from Drug Control Committee (DCC) meeting.Receiving sample testing and product renewal approval.Collecting No Objection Certificate (NOC) and drug clearance approval.Building and maintaining better relationship with regulatory authority personnel of DGDA.Liaising and negotiating with regulatory authorities.Preparing various documentations.
Maters in any discipline preferably in Pharmacy from any UGC recognized university.
1 to 2 year(s)
The applicants should have experience in the following area(s):
Drug Rules Regulations, Regulatory Affairs
The applicants should have experience in the following business area(s):
Oct. 28, 2020, midnight