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⏰ Full-time

Regulatory Affairs Specialist

ProductLife Group
Location πŸ“ remote, India
Posted πŸ“… June 07, 2026
Work Type ⏰ Full-time

Position Overview

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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Job Details

⏰
Employment Type
Full-time
πŸ“Š
Category
Other-General
🏠
Work Arrangement
On-site
πŸ“
Location
remote, India