Executive – India Regulatory Affairs, Vadodara

This Vadodara regulatory role handles Indian filings: reviewing CMC and other documents, compiling dossiers and submitting to CDSCO for trial, BE, manufacturing and import permissions, post-approval changes, IPC testing dossiers, label artwork checks and prescribing information. M.Pharm with at least 2 to 5 years of relevant experience is listed. Apply on the official Sun Pharma careers page.