Drug Regulatory Affairs Executive

-Prepare, review, and submit CTD/eCTD/ACTD dossiers for international product registrations. -Ensure compliance with regulatory requirements in EU, US, Asia, CIS, LATAM, and Africa. -Coordinate with regulatory agencies/client for product approvals.°Bachelor’s/Master’s degree in Pharmacy, Pharmaceutical Sciences 3–5 years of experience in international regulatory affairs. Strong knowledge of ICH, WHO-GMP, and country-spec regulatory guidelines.°