Regulatory Affairs Specialist

ProductLife Group

Full-time Other-General
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Location
Remote, Remote, India
Posted
July 09, 2026

Job 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/Co-ordination with client and participate ...

    • Job Details

    • Job Type
      Full-time
    • Category
      Other-General
    • Date Posted
      July 09, 2026
    • Application Deadline
      August 18, 2026