Full-time

Regulatory Affairs Specialist

Posted by ProductLife Group • June 07, 2026

📍 remote, remote, India
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Description

A Specialist profile will ensure efficient project execution, better quality outcomes, and reduced dependency on supervision. Therefore, hiring a Specialist is essential to meet the role requirements effectively.



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.
  • Support for Initial MA application, all kind of LCM activities.
  • Act as (Single) Point of Contact and oversee clients’ portfolios.
  • Cross-functional co-ordination.
  • Communication with external vendors.
  • Communication...

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