Key Responsibilities
1. Dossier Preparation & Submissions
- Prepare, review, and submit CTD / ACTD / country‑specific dossiers for:
- New product registrations
- Line extensions (strength, pack size, shelf life)
- Variations and renewals
- Coordinate compilation of Modules 1–5 with QA, QC, R&D, CMC, PV, PM, and Manufacturing teams.
- Ensure dossier compliance with WHO, ICH, and local authority guidelines.
2. Regulatory Strategy & Market Support
- Support business development by providing regulatory feasibility and timelines for new markets/products.
- Assess regulatory impact for formulation/site changes.
3. Regulatory Lifecycle Management
- Manage post‑approval changes, including:
- CMC variations
- Labeling updates
- Artwork changes
- Track and ensure timely renewals/re‑registrations.
- Maintain approved product documentation and regulatory databases.
4. Health Authority Interaction
- Handle deficiency letters / queries from regulatory agencies.
- Prepare responses in coordination with internal stakeholders.
- Liaise with local agents, consultants, and partners for RoW countries whenever required.
5. Compliance & Intelligence
- Monitor regulatory guideline updates for RoW markets.
- Ensure submissions comply with the latest country requirements.
Markets Typically Covered (RoW)
- LATAM: Brazil, Mexico, Colombia, Peru, Chile, Guatemala
- MENA/GCC region
- CIS: Russia, Ukraine, Kazakhstan, etc.
- ASEAN: Philippines, Vietnam, Thailand, Malaysia, etc.
Qualifications
Required Qualifications & Experience
• Educational Background:
o M.Pharm / B.Pharm
• Experience:
o 3-9 years in Pharmaceutical Regulatory Affairs
