Thực tập sinh Đăng ký sản phẩm (Regulatory Affairs Intern)

Introduction
Qualtech is an Asia 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 be able to understand to 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.
Job description

Investigating proactively and capitalizing regulatory information collected throughout studies and maintain Regulatory database accordingly.
Ability to read and understand regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information, and complex documents.
Other duties as assigned.
Oversight of regulatory submissions for assigned projects/countries, which may include completion of submissions or notifications, as required.

Requirements

Ability to manage multiple projects, set priorities to meet deadlines.
Fluent in Englishis a must, in other languages will be an advantage. Candidates who can speak Chinese will be a big plus.
Only recruiting female candidates.
Strong interpersonal skills, both written and oral.
Basic skills in MS Office: Word, PowerPoint, Excel, Outlook.
Can workat least 24hours per weekfor a duration of4to 6 months.
Keeping attention to details.
Fresh graduates for senior students in related majors, such as biomedical engineering, biotechnology and medicinal chemistry

Benefits

Have chances to become a full- time employee.
Allowance:Thehourly rateranges fromVND 40,000 to 50,000, depending on ability.
Professional, dynamic working environment.
Confirmation of completing the internship.

Cập nhật gần nhất lúc: 2024-07-19 06:10:02