Posted:2 days ago|
Platform:
Work from Office
Full Time
Qualification: Bpharm/Mpharm Experience: 4-5 yrs in Drug Product regulatory affairs Job Responsibilities: should have experience in the Preparation and review of European Dossiers including 2-5 modules. Should have experience in the compilation of Module -1 Should have knowledge of EU variations Able to run independently EU procedures such as DCP and National. Working experience in eCTD is required Skills: Good written skills Knowledge in computers Good analytical skills
Vizen Life Sciences
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