Công ty TNHH Qualtech Consulting tuyển vị trí Đăng ký sản phẩm thiết bị y tế (Regulatory Affairs Intern)

Job description

• 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.

Requirements

• 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, medicinal chemistry.
• Fluent in English is a must, in other language 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.

Benefits

• Allowance: VND 50,000/hour.
• Confirmation of completing the internship.
• Have a chance to become a full-time employee.
• Professional, dynamic working environment.

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

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

Deadline for application: February 7, 2025

Contact window: Please send your resume and cover letter to Ms. Vivian (vivian@qualtechs.com).