Regulatory Affairs Specialist

1 week ago


Mumbai, Maharashtra, India BEST-FIT Recruitment Riders Full time

Job Profile:

  • Responsible for collecting and preparing plant-level documents for regulatory submissions, following registration guidelines of different countries, and regulatory submissions.
  • Prepare and submit variations to authorities, following up on submissions, timelines, and approvals with the concerned person.
  • Familiarity with CTD formats and dossier preparation is essential.
  • Ensure timely sample dispatch and coordinate with the concerned person for submission, receipt, and follow-up on registrations.
  • Verify COAs before dispatching Commercial Orders.
  • Apply Product Permissions, COPPs, and coordinate for the addition of New Products in the WHO GMP List.
  • Verify artwork and leaflets for both International and Domestic Supplies.
  • Participate in writing and updating SOP / Work Instructions and process improvements.
  • Travel to Manufacturing Units during audits by External Agencies.

Desired Profile:

  • B. Pharm / M. Pharm with 4.0 to 7.0 years of experience in Regulatory Affairs in Formulation with growing Pharma in Semi-Regulated / ROW markets.
  • Should have a good understanding of Regulatory Affairs life cycle for Solid Oral, Parenteral & Topical Formulations.
  • Strong writing and communication skills in English are required.


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