Mô tả công việc

In process control at production area.
Manage workers, materials, procedures to produce qualified products.
Perform internal audits and assist in external audits/inspections.
Participate in investigations related to product quality issues and ensure timely closure.
Coordinate with cross-functional teams for continual quality improvements.
Issue batch record for production, receive and review batch records.
Compile and update SOP, product master file, annual product review, …
Support GMP periodic training, validate manufacturing process, and follow other duties required from QA Manager.

Official Education: Pharmacy/ Chemistry/ Biology University
Supplementary Certificate
Strong communication and interpersonal skills
Proficient in MS Office
Good command of English
Experience in QA or a similar role in the pharmaceutical industry.
Familiarity with regulatory guidelines (e.g., GMP, CFR, ISO,…)
Fresh graduates with Pharmacy degrees and a strong willingness to learn
Can work in shifts (4 shifts: 06:00 - 14:00; 14:00 - 22:00; 22:00 - 06:00; 08:00 - 17:00), shift change per week

Thông tin tham khảo

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Nguồn tin: Nguồn: CareerViet · đăng 09/08/2026