SEI Optifrontier VIỆT NAM

Chi tiết
Working location: Lang Ha, Ba Dinh, Ha Noi
Working time: 8:00 - 17:00, Mon-Fri
I. Major Responsibilities:
1. Regulatory Affairs:
- Prepare, submit, and follow up the product's registration with MOH
- Cooperate with relevant departments (marketing, field force) to prepare and submit the products brochure to get approval of MOH
- Update reports, systems as required
- Conduct the regulatory surveys, communicate with Regional for registration products
- Other tasks assigned by manager
2-Quality Assurance:
- Receive product quality complaint (PQC) within Vietnam and report to manufacturer and OIAA-QA
- Monthly reconciliation with distributor for PQC
- Update reports, systems as requiredYêu cầu
II. Qualifications/Experience (Required Knowledge, Skills, Education, Relevant Experience):
- Bachelor's degree of Pharmacy
- Having at least 1 year experience in the regulatory affairs positions for imported drugs
- MS Office (Outlook, PowerPoint, Excel and Word) proficiency
- Bilingual in English and Vietnamese (written, spoken)
III. Competencies:
- Strong administration and attention to detail
- Good communication and interpersonal skills
- Ability to consistently meet deadlinesQuyền lợi
- Competitive salary
- Full insurance according to law
- Other benefit according to company policy