Full-time

Regulatory Affairs Officer

Posted by ProductLife Group • June 07, 2026

📍 India, India, India
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Description

MAIN ACTIVITIES FOR THE JOB

  • Contribute to regulatory activities performed on the RA Platform/the Hub.
  • Regulatory activities include pre licensing activities, new registration (sites and medicinal products), post licensing regulatory submissions, interaction with health authorities on behalf of PLG customers.
  • To contribute to the production of client administrative documents and reports to be included in regulatory submissions.
  • Compile, or supervise the compilation of regulatory dossiers in accordance with national requirements.
  • Systems Management and Administration.
  • Document and track regulatory submissions and regulatory authority approval.
  • Gain regulatory authority approval.
  • Provide regulatory support to clients and associate companies.
  • Liaise with sponsor head-office and affiliate departments on regulatory issues.
  • Liaise with external regulatory authorities as required. ...

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