Thực Tập Sinh Đăng Ký Sản Phẩm

Job Description

Qualtech is a Medical Device Consulting and Clinical Trial (CRO) Company with branch offices in China, Hong Kong, Indonesia, Japan, Malaysia, Philippines, Singapore, Vietnam, Thailand, Korea, USA and Germany. We are looking for a talented Regulatory Affairs Intern who is fluent in English and is able to understand medical device regulations in the countries we service for.

Qualtech is committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people.

• 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.

Job Requirement

• 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.