Officer/Executive (RA)

3 - 8 years

2 - 7 Lacs

Posted:3 days ago| Platform: Naukri logo

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Work Mode

Work from Office

Job Type

Full Time

Job Description

Roles and Responsibilities

  • Prepare dossiers for regulatory submissions, including CTD/eCTD format.
  • Ensure compliance with USFDA regulations through dossier compilation and submission.
  • Manage RA activities from pre-clinical to post-marketing stages, covering both domestic and international markets.
  • Develop expertise in drug regulatory affairs, focusing on row market requirements.
  • Collaborate with cross-functional teams to ensure timely completion of projects.

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Biomatrix Healthcare logo
Biomatrix Healthcare

Healthcare

San Francisco

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