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1.0 - 5.0 years

0 Lacs

navi mumbai, maharashtra

On-site

Role Overview: As a Regulatory Affairs Associate at Teva, you will be a project manager responsible for the Regulatory Affairs lifecycle management on Medis dossiers for Teva's 3rd party client business (Medis). Your main task will involve ensuring that information flow and provision of supportive documents reach the clients. You will be liaising with Teva's 3rd party client business (Medis) supply chain, Teva site RA, and other relevant functions. Your role will focus on lifecycle management of specific products for Europe and the international market, ensuring regulatory modules under your responsibility are up to date and in accordance with agreed procedures. Key Responsibilities: - Infor...

Posted 4 days ago

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