CHUYÊN VIÊN QC (HÓA LÝ) / PHYSICO-CHEMICAL SUPERVISOR
Văn phòng đại diện Orioled Hub Sia tại Thành phố Hồ Chí Minh
Địa điểm làm việc: Hồ Chí Minh, Bà Rịa - Vũng Tàu
Hết hạn: 10/11/2024
- Chi tiết công việc
- Giới thiệu công ty
Thu nhập: Cạnh tranh
Loại hình: Toàn thời gian
Chức vụ: Nhân viên
Mô tả công việc
Mô tả Công việc
1. Preparation/ review documents (80%)
Responsible for preparation/ review of documents such as but no limited: SOPs, specifications, testing procedures, analytical datasheets, trend analysis, risk assessment, etc.
Preparation of User Requirements Specification, operating & cleaning procedure, documents for calibration/ validation/ qualification/ maintenance, monitoring the qualification and calibration status of equipment.
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.
Test raw materials, intermediate products, bulk products and finished products.
2. Other works (20%)
Following instructions and reporting directly to the Head of QC department
Taking other tasks which are assigned by the Head of QC department
Responsible for preparation/ review of documents such as but no limited: SOPs, specifications, testing procedures, analytical datasheets, trend analysis, risk assessment, etc.
Preparation of User Requirements Specification, operating & cleaning procedure, documents for calibration/ validation/ qualification/ maintenance, monitoring the qualification and calibration status of equipment.
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.
Test raw materials, intermediate products, bulk products and finished products.
Following instructions and reporting directly to the Head of QC department
Taking other tasks which are assigned by the Head of QC department
1. Preparation/ review documents (80%)
Responsible for preparation/ review of documents such as but no limited: SOPs, specifications, testing procedures, analytical datasheets, trend analysis, risk assessment, etc.
Preparation of User Requirements Specification, operating & cleaning procedure, documents for calibration/ validation/ qualification/ maintenance, monitoring the qualification and calibration status of equipment.
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.
Test raw materials, intermediate products, bulk products and finished products.
2. Other works (20%)
Following instructions and reporting directly to the Head of QC department
Taking other tasks which are assigned by the Head of QC department
Responsible for preparation/ review of documents such as but no limited: SOPs, specifications, testing procedures, analytical datasheets, trend analysis, risk assessment, etc.
Preparation of User Requirements Specification, operating & cleaning procedure, documents for calibration/ validation/ qualification/ maintenance, monitoring the qualification and calibration status of equipment.
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.
Test raw materials, intermediate products, bulk products and finished products.
Following instructions and reporting directly to the Head of QC department
Taking other tasks which are assigned by the Head of QC department
Yêu cầu
Yêu Cầu Công Việc
- 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:
English: Reading comprehensive documents in the pharmaceutical sector, good at communication and writing skills
Office skills: Effectively using office applications including Word, Excel, PowerPoint, etc.
Others/Khác: be active in tasks, self-studied, and friendly with colleagues.
- 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:
English: Reading comprehensive documents in the pharmaceutical sector, good at communication and writing skills
Office skills: Effectively using office applications including Word, Excel, PowerPoint, etc.
Others/Khác: be active in tasks, self-studied, and friendly with colleagues.
Quyền lợi
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
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
Thông tin khác
Bằng cấp:
Đại học
Độ tuổi:
Không giới hạn tuổi
Lương:
Cạnh tranh
Đại học
Độ tuổi:
Không giới hạn tuổi
Lương:
Cạnh tranh
Thông tin chung
- Thu nhập: Cạnh tranh
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