Tuyển dụng Nhân viên Đảm bảo chất lượng (QA), Đăng ký thuốc (RA)

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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

- Keep up to date with changes in regulatory legislation and guidelines

- Update reports, systems as required

- 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 required

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II. Qualifications/Experience (Required Knowledge, Skills, Education, Relevant Experience):

- Bachelor’s degree of Pharmacy

- Having experience in the pharmaceutical industry in regulatory affairs

- 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 deadlines