Quality Management Assistant Manager
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 công việc
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 Master's 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
Phân tích mức độ cạnh tranh
VietnamWorks AI
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Giá
29.000đ / lượt
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Thưởng
Đào tạo
Xe đưa đón
Thông tin việc làm
19/12/2024
Trưởng phòng
Sản Xuất > Đảm Bảo Chất Lượng/Kiểm Soát Chất Lượng/Quản Lý Chất Lượng
Auditing, Calibration, ISO Standards, Quality Management System, Quality Assurance
Thiết bị y tế
Bất kỳ
3
Người Việt Nam
Địa điểm làm việc
Thanh Oai Industrial Complex Thanh Oai Dist, Hanoi Vietnam
Thanh Oai Industrial Complex, Thanh Oai Dist, Hanoi, Vietnam
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