PHARBEST PHARMACEUTICALS INC. Jobs

Primary responsibility is to compile, review, and submit various regulatory filings. o *IND* (Investigational New Drug). o *NDA/ANDA/BLA* (New Drug Application/Abbreviated New Drug Application/Biologics License Application). o *DMF* (Drug Master File). o Compile CTD/eCTD Modules. o Ensure submissions follow *country-specific regulatory guidelines* (FDA, EMA, MHRA, WHO, ICH). o Monitor and interpret *changes in global regulations*, guidance docume...