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Regulatory Affairs Specialist – Nhân Viên Đăng Ký Thuốc, Từ 3 - 5 Năm Kinh Nghiệm

Công Ty TNHH Dược Phẩm New Far East

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...

Regulatory AffairsDrug RegistrationGmp

This is a summary. The full description and the application form are on VietnamWorks.