Kinh nghiệm làm việc:
Từ 1 đến 2 năm cho vị trí tương đương
Giới tính: Không yêu cầu
Cấp bậc: Nhân viên
Mô tả công việc
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
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