RV GROUP VIỆT NAM

Responsibilities:

• Review of products Dossiers for Drug formulation, Food supplements and submit to DAV, VFA as per requirement
• Regulatory submission for Imported as well as some of the Local products
• Technical support for Technology transfer projects for Group companies
• Review and submission of technical documents for Tender application
• Candidate will be responsible for GMP registration required for Tender application
• Follow up DAV expert and VFA expert to get registration approval within deadline given by company
• Support company in commercial supply by providing technical documents to Marketing team as and when necessary
• Perform other tasks required by Line Manager

Requirement:

Work Experience

• Graduated from medical university.
• Responsibility to work, hard work, good self-learning ability, initiative and positive thinking.
• 2-3 years of experience in drug registration.
• Good organizational and time management skills.

- Having chances to get attractive company bonus every month/year

- Company trip once a year + Joining party

- Salary and position is reviewed 1 time a year

- Bonus by individual ability and company’s performance.

- Social insurance, health insurance, unemployment insurance and other benefits

- Dynamic and sociable working environment.