Regulatory Affairs Specialist Full-time

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 capitalising on regulatory information collected throughout studies and maintaining the regulatory database accordingly.

Support the tasks for the Sales team.

Other duties as assigned.

Major in related majors, such as biomedical engineering, biotechnology, and medicinal chemistry.

Fluency in English is a must; fluency in other languages will be an advantage.

Candidates who can speak Chinese will be a big plus.

At least one year of experience in the RA field.

Ability to manage multiple projects and set priorities to meet deadlines.

Attention to detail.

Strong interpersonal skills, both written and oral.

Basic skills in MS Office: Word, PowerPoint, Excel, Outlook.

Gender: Female Prioritise Quang Ngai residents

Salary: negotiated Social Insurance, Medical Insurance, Unemployment Insurance

benefits:. 13th month pay (shall have worked consecutively for 1 year). Annual leave with pay Professional, dynamic working environment. Have a chance for overseas training