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POSITION OVERVIEW | TỔNG QUAN VỊ TRÍ We are seeking a highly competent Regulatory Affairs Specialist to manage regulatory activities for imported pharmaceutical products in Vietnam. The role involves end-to-end responsibility for drug registration lifecycle, regulatory strategy, and post-marketing compliance, ensuring alignment with Ministry of Health (MOH) regulations and international pharmaceutical standards. Chúng tôi đang tìm kiếm... • Minimum 3–5 years of hands-on experience in pharmaceutical regulatory affairs, with a focus on drug registration for imported products in the most recent role. Tối thiểu 3-5 năm kinh nghiệm thực chiến RA, đặc biệt đăng ký thuốc nhập khẩu tại vị trí công việc gần nhất. • Strong knowledge of Vietnamese MOH regulations, CTD structure, GMP...