Quận Cầu Giấy 12/04/2024 6 - 8 triệu VNĐ
Huyện Quốc Oai 13/04/2024 20 - 30 triệu VNĐ
Quận Nam Từ Liêm 19/04/2024 Thỏa thuận
Quận Hoàng Mai 25/04/2024 9 - 12 triệu VNĐ
Huyện Mê Linh 30/03/2024 Thỏa thuận
Huyện Mê Linh 06/04/2024 Thỏa thuận
Huyện Mê Linh 06/04/2024 Thỏa thuận
Huyện Đông Anh 21/04/2024 Từ 16 triệu VNĐ
Quận Hai Bà Trưng 22/04/2024 Đến 4 triệu VNĐ
Huyện Quốc Oai 26/04/2024 13 - 20 triệu VNĐ
Tính chất công việc
Full-time
Vị trí/chức vụ
Nhân Viên/Chuyên Viên
Ngày đăng tuyển
27/04/2021
Yêu cầu bằng cấp (tối thiểu)
Đại Học
Yêu cầu kinh nghiệm
Không yêu cầu
Yêu cầu ngôn ngữ
Địa điểm làm việc
Be responsible to plan, conduct validation and follow-up re-validation in accordance with B. Braun's Validation SOPs, such as Design Qualification, Installation Qualification, Operational Qualification, Performance Qualification and Releasing Final Validation Report for all production processes in production facility.
This includes as followings:
- Create, monitor and follow the Master Validation Plan for production processes/equipment used for producing and quality controlling at the plants of BBV - Co-ordinate with the QC, QM and Production to make a risk assessment then define and perform needed activities related to Qualification and Validation of equipment and processes according to Validation Master Plan or department's requests, as well as WHO GMP/ISO 9001/ ISO 13485 requirements
- Monitor and co-ordinate with related persons to undertake quality engineering projects with guidance from the Superior and the Management in co-operation with
Production and Quality Control department. To ensure that the validation and calibration activities are undertaken objectively based on clear technical aspects
- Assist other QM function for performing process audit arise due to corrective actions implementation
- Plan and execute qualifications and validation computerized system validation, data integrity and other as request.
- Implement Corrective Action and Preventive Action, Risk assessment, Deviation Control
- Prepare validation document to support drug registration activities (if any)
- Implement other quality issues whenever required
- Ensure that the requirements of ISO, GMP, GSP. GLP as well as legal requirements are well implemented and maintained
- Ensures that the Pharma audit programs are developed and executed effectively
- Handles complaints system from clients and product regulatory affair processes
- Graduated from universities with technical engineering background
- Good command of English both in communicating & writing
- Have working experience in pharmaceutical/ medical device manufacturing is an advantage
- Understand well applicable quality standards (WHO GMP; ISO 9001: ISO 13485 where applicable)
- Having chances to get attractive company bonus every month/year
- Company trip once a year + Joining party
- Salary and position is reviewed 1 time a year
- Bonus by individual ability and company’s performance.
- Social insurance, health insurance, unemployment insurance and other benefits
- Dynamic and sociable working environment.
Thanh Oai Industrial Complex, Thanh Oai Dist, Ha Noi, Viet Nam
>500 nhân viên
Công ty Dược phẩm B.Braun được thành lập năm 1839 tại Mensulgen - Đức; là một công ty hàng đầu về lĩnh vực sản xuất dược phẩm và dụng cụ y tế với trên 160 năm kinh nghiệm, B.Braun... [Xem thêm]
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