Mô tả công việc
Oversight of regulatory submissions for assigned projects/countries, which may include completion of submissions or notifications, as required.
Ability to read and understand regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information, and complex documents.
Investigating proactively and capitalizing regulatory information collected throughout studies and maintain Regulatory database accordingly.
Other duties as assigned.
Yêu cầu công việc
Can work at least 24 hours per week for a duration of 4 months to 6 months.
Fresh graduates for senior students in related majors, such as biomedical engineering, biotechnology,
pharmaceutical.
Fluent in English is a must, in other languages will be an advantage. Candidates who can speak Chinese will be a big plus.
Ability to manage multiple projects, set priorities to meet deadlines.
Keeping attention to details.
Strong interpersonal skills, in written and oral.
Basic skills in MS Office: Word, PowerPoint, Excel, Outlook.
Quyền lợi được hưởng
Allowance: The hourly rate ranges from VND 40,000 to 50,000, depending on ability.
Confirmation on completing the internship.
Have chances to become a full-time employee.
Professional, dynamic working environment.
Thông tin khác
Cấp bậc
Thực tập sinhKinh nghiệm
Không yêu cầu kinh nghiệm
Số lượng tuyển
1 người
Hình thức làm việc
Thực tập
Giới tính
Không yêu cầu
Nộp hồ sơ liên hệ
Công ty TNHH Qualtech Consulting
