JOB DESCRIPTION: Executive-Drug Regulatory Affairs
Responsibilities
· To prepare dossiers in ACTD, CTD and country specific formats.
· To review the Drug Master file (DMF) as per the requirements.
· Documentation work for procuring product permission, COPP, FSC & NOC
· To resolve queries received from HOH consultants within the deadline.
· To review the technical document QA – QC and productions.
· To coordination with QA – QC and other departments for required documents to dossier preparation and compilation
· To collect & dispatch the dossier samples as per requirements of various countries.
· To review Artwork as per the requirements.
Pay: From ₹15,000.00 per month
Work Location: Remote
