Executive, Regulatory Affairs

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 .

1. Regulatory Strategy & Market Support

• Support business development by providing regulatory feasibility and timelines for new markets/products.
• Assess regulatory impact for formulation/site changes.

1. 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.

1. 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.

1. 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.

Required Qualifications & Experience

• Educational Background:

o M.Pharm / B.Pharm

• Experience:

o 3-9 years in Pharmaceutical Regulatory Affairs