CHUYÊN VIÊN QC (HÓA LÝ) / PHYSICO-CHEMICAL SUPERVISOR

Preparation/ review documents (80%)

Preparation of protocols for method validation and conducting tests for analytical method validation based on the protocol.
Preparation of protocols for stability study and evaluate, monitor the stability sample of the product under study.
Preparation of User Requirements Specification, operating & cleaning procedure, documents for calibration/ validation/ qualification/ maintenance, monitoring the qualification and calibration status of equipment.
Test raw materials, intermediate products, bulk products and finished products.
Responsible for preparation/ review of documents such as but no limited: SOPs, specifications, testing procedures, analytical datasheets, trend analysis, risk assessment, etc.

Other works (20%)

Taking other tasks which are assigned by the Head of QC department
Following instructions and reporting directly to the Head of QC department

- Education: Bachelor’s degree in chemical or pharmaceutical sectors
- Experience: Preference will be given to candidates with experience in pharmaceutical industry, especially EU GMP factory.
- Skills:

Office skills: Effectively using office applications including Word, Excel, PowerPoint, etc.
Others/Khác: be active in tasks, self- studied, and friendly with colleagues.
English: Reading comprehensive documents in the pharmaceutical sector, good at communication and writing skills

Laptop, Chế độ bảo hiểm, Du Lịch, Phụ cấp, Đồng phục, Chế độ thưởng, Chăm sóc sức khỏe, Đào tạo, Tăng lương, Công tác phí, Phụ cấp thâm niên, Nghỉ phép năm, CLB thể thao

Cập nhật gần nhất lúc: 2024-10-16 10:50:03