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2.0 - 6.0 years

0 Lacs

maharashtra

On-site

You will be responsible for handling regulatory affairs in XEVMPD (Extended Eudravigilance Medicinal Products Dictionary) and RIMS. The ideal candidate should have a minimum of 2-5 years of relevant experience in this field. Additionally, experience in veeva-vault for creating RO/SO events, XEVMPD submission, and knowledge of IDMP and QMS database will be beneficial for this role. The position is based in Mumbai.,

Posted 6 days ago

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