Kinh nghiệm: 6
Yêu cầu bằng cấp: Cử nhân
Số lượng cần tuyển: 1
Ngành nghề: Medical, Sản xuất, QA, QC, Kiểm nghiệm
Địa điểm làm việc: Hà Nội
Chức vụ: Quản lý
Hình thức làm việc: Mọi hình thức
Yêu cầu giới tính: Nam/ Nữ
Yêu cầu
- Bachelor degree in technical or pharmacy field
- More than 6 years of related working experience in quality management in manufacturing environment, medical devices/ pharmaceutical industry preferred
- Experience in leading a team
- Standard: ISO 9001, ISO 19011, ISO 14644, GMP ; 5whys analysis
- Good English and communication skill
- Auditting, reporting, presentation, troubleshooting skill
Quyền lợi
Competitive salary and attractive annual bonus
Production incentive
Guaranteed 13th month salary
Company health insurance
Responsibility allowance
Service award
Company canteen or lunch allowance
Company shuttle bus
Exciting company engagement activities
Chi tiết
Are you a Quality Management Assistant Manager passionate about quality management? If so, this opportunity could be for you! Join us in Hanoi at B. Braun, a leader in the medical devices industry, where your skills and experience will be recognized and celebrated. Take the next step in your career with us and help shape the future of healthcare!
As a Quality Management Assistant Manager at B. Braun, you will play a vital role in administering quality management system of the assigned production facilities.
Main job responsibilities:
- Assist QM Manger to ensure establishment and maintenance of the quality management system to meet WHO GMP, ISO as well as other regulatory and company requirements, include lead responsible for reviewing & revising QM documents.
- Properly apply production and operation controls to meet GMP, ISO and related regulatory requirements.
- Control and monitor the quality performance objective.
- Establish and lead the annual audit program (internal, external and division…) including unplanned audit and inspection.
- Coordinate and follow up the CAPA, Customer Complaints, Audits, Change Control, Risk Management with relevant stakeholders to ensure all matters are solved properly and in accordance with requirements, verify improvement actions and evidence.
- Prepare quality reports and any information that required.
- Act as local safety officer to execute properly relevant SOPs for this responsibility including Recall, HHA, Vigilance.
- Evaluate, assessment and give final QM statement for IC & PC complaints on SAP C3, and DIR, CAPA… on B.TraQS
- Coordinate with relevant stakeholders to ensure the technical registration of B.Braun Vietnam at oversea market to be provided properly and on time in full.
- Supervise, develop team members and provide the on-the-job coach and guidance.
