Regulatory Affairs Specialist
1 week ago
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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