3 - 8 years
6.0 - 11.0 Lacs P.A.
Dera Bassi
Posted:2 months ago| Platform:
Work from Office
Full Time
Responsible to review and submission of DMFs/E-DMFs/CEPs to US-FDA, Europe Exposure to Export Regulatory Market Quality and speedy response to the Regulatory agencies queries and Customer queries. Required Candidate profile Review and submission to drug listing (Label) of our API to US-FDA Maintaining the life cycle of submitted DMFs, annual-updates, amendments and variation filings as per the stipulated timeline
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