Thực Tập Sinh Đăng Ký Sản Phẩm 2025

• Oversight of regulatory submissions for assigned projects/countries, including preparation and completion of submissions or notifications as required.
• Read and understand regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information, and other related documents.
• Proactively investigate and compile regulatory information gathered during projects; maintain the regulatory database accordingly.
• Other duties as assigned.

Location: 139 Nguyen Thi Nhung Street, Van Phuc Urban Area, Hiep Binh Phuoc Ward, Thu Duc City, Ho Chi Minh City, Vietnam

Working time: 8:00-17:00, Monday-Friday

Deadline for application: June 30, 2025

• Female candidates only.
• Able to work at least 24 hours per week for a period of 4 to 6 months.
• Fresh graduates or senior students in related majors such as Biomedical Engineering, Biotechnology, or Medicinal Chemistry.
• Fluent in English (spoken and written). Candidates who can speak Chinese will be a big plus.
• Ability to manage multiple projects and set priorities to meet deadlines.
• Attention to detail, responsible, and organized.
• Strong interpersonal skills, both written and oral.
• Basic skills in MS Office: Word, PowerPoint, Excel, Outlook.