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Regulatory Affairs Executive

4 - 5 years

6 - 7 Lacs

Posted:3 weeks ago| Platform: Naukri logo

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Full Time

Job Description

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

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Vizen Life Sciences
Vizen Life Sciences

Biotechnology

San Francisco

50-100 Employees

5 Jobs

    Key People

  • Dr. Alice Johnson

    CEO
  • Mark Smith

    CTO

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