Check with seller Tuyển dụng Hà Nội Tập Đoàn B. Braun Việt Nam cần tuyển

[Tuyển dụng Hà Nội] Tập Đoàn B. Braun Việt Nam cần tuyển Chi tiết công việc

Giới thiệu công ty



Thu nhập:
Thương lượng
Loại hình:
Toàn thời gian





Chức vụ:
Nhân viên





Kinh nghiệm:
6 năm
sản xuất
iso
audit
communication
Mô tả công việc
Job Purpose: This position will assist QM manager to ensure the establishment and maintenance of the quality management system to meet WHO GMP, ISO as well as other regulatory and company requirements. This role will supervise team members and provide on-the-job coaching and guidance.
Task & Responsibilities:
1. Assist QM manager to ensure establishment and maintenance of the quality management system to meet WHO GMP, ISO as well as other regulatory and company requirements including:
• Creating, reviewing & revising QM documents. Properly apply production and operation controls to meet GMP, ISO and related regulatory requirements.
• Establish and lead the annual audit program (internal, external and division...) including unplanned audits and inspections.
• Review and finalize QM final statement on deviation, CAPA, audits at B.TraQs system and customer complaints at SAP system based on the investigations and feedback of respective stakeholders.
• 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, including verifying improvement actions and evidence.
• Act as local medical device and nutrient safety officer, including executing relevant SOPs for this responsibility: Recall, HHA, Medico Vigilance.
• Coordinate with relevant stakeholders to ensure the technical registration of BBVN at overseas market to be provided properly and on time in full.
2. Quality records & reports:
• Respond to provide quality reports: weekly, monthly, quarterly, yearly both local and global sides.
• Control and monitor Quality Indicator Performance and QM dashboard.
3. Local Safety Officer:
• Maintain and monitor the pharmaco, medico vigilance system.
• Follow the responsibility about pharmaco vigilance mentioned in affected SOP.
• Perform tasks about pharmaco vigilance, medico vigilance as affected SOP.
4. Team Management:
• Manage Compliance & SQM team and Document & Customer Complaint team.
• Supervise, coach, be responsible for performance and career development guidance to team members.
• Control qualification matrix of QM team and define training plan for team accordingly.
5. Other tasks:
• Project management.
• Join the defined meetings planned and unplanned, join training batches...
Yêu cầu
Requirement:
1. Education:
Must have:
• Bachelor degree in Technical background
• Quality background knowledge
• Technical background knowledge
• Standard: ISO 9001, ISO 19011, ISO 14644, GMP
• 5whys analysis
Nice to have:
• Pharmaceuticals background is preferred.
• ISO 13485 is preferred.
• ISO 14001, ISO 45001 - 6 Sigma, SPC
• Vietnam regulatory relating to Medical device and Calibration
2. Working Experience
• Must have: 6 years of related working experience or Masters degree with 3 years of related working experience
• Nice to have: Auditor, QC, Production, RA
3. Skills:
• Fluent in English
• Communication, Auditing, Reporting, Presentation, Troubleshooting, Leadership
• Training and coaching skill
Quyền lợi
Thưởng
Attractive performance bonus & salary review
Đào tạo
International working environment with many training opportunities
Xe đưa đón
Company bus from the central to company
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Thông tin khác
NGÀY ĐĂNG
19/12/2024
CẤP BẬC
Trưởng phòng
NGÀNH NGHỀ
Sản Xuất > Đảm Bảo Chất Lượng/Kiểm Soát Chất Lượng/Quản Lý Chất Lượng
KỸ NĂNG
Auditing, Calibration, ISO Standards, Quality Management System, Quality Assurance
LĨNH VỰC
Thiết bị y tế
NGÔN NGỮ TRÌNH BÀY HỒ SƠ
Bất kỳ
SỐ NĂM KINH NGHIỆM TỐI THIỂU
3
QUỐC TỊCH
Người Việt Nam
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Thông tin chung
Thu nhập: Thương lượng
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