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 maintaining 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.
  • Only recruiting female candidates. (Please send your resume in English)
Phúc lợi công việc
  • 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.
Cách thức ứng tuyển

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Logo Công ty TNHH Qualtech Consulting Công ty TNHH Qualtech Consulting
139 Nguyen Thi Nhung Street, Van Phuc urban area, Hiep Binh Phuoc Ward, Thu Duc, Ho Chi Minh City
Quy mô: ít hơn 10 nhân viên

Ngày đăng tuyển
02/05/2024

Nơi làm việc
Tp Hồ Chí Minh

Cấp bậc
Mới tốt nghiệp/Thực tập

Ngành nghề
Dịch vụ pháp lýKhác

Kỹ năng
Medical devices, Medical device registration, Technical documents

Ngôn ngữ trình bày hồ sơ
Tiếng Anh

Trình độ học vấn
Đại học

Ứng viên
Nữ
Regulatory Affairs Intern
Công ty TNHH Qualtech Consulting
Nộp đơn