CÔNG TY TNHH QUALTECH CONSULTING TUYỂN DỤNG

CÔNG TY TNHH QUALTECH CONSULTING TUYỂN DỤNG

Position Title: Global Regulatory Affairs Specialist

Job description

- Oversight of regulatory submissions for assigned projects/countries, which may include completion of submissions or notifications, as required.

- Independently interacts and builds partnerships with competent authorities.

- Ability to read and understand regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information, and complex documents.

- Providing advice and support to the project team for regulatory or technical aspects of the projects.

- Investigating proactively and capitalizing regulatory information collected throughout studies and maintain Regulatory database accordingly.

- Other duties as assigned.

Requirements

- Preferably Bachelor students or above. Knowledge in medical-related field will be a plus.

- 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.

- Keen attention to details.

- Strong interpersonal skills, in written and oral.

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

- Work location: 236/43/2 Điện Biên Phủ St, 17 Ward, Bình Thạnh District,  Hồ Chí Minh City.

- Time: 8:00-17:00 Monday – Friday

- Salary: 9 – 13m VND

Benefit

- Bonus 13th salary and Performance bonus

- Insurance & Paid-leaves as required by Labor Law

- Professional, dynamic working environment

- Domestic and overseas training opportunities.

Deadline for application: April 30th, 2021

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