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Địa điểm

Hải Phòng

  • Lương

    Cạnh tranh

  • Kinh nghiệm

    1 - 2 Năm

  • Cấp bậc

    Nhân viên

  • Hết hạn nộp

    31/07/2026

Phúc lợi

  • Chế độ bảo hiểm
  • Du Lịch
  • Phụ cấp
  • Chế độ thưởng
  • Chăm sóc sức khỏe
  • Đào tạo
  • Tăng lương
  • Nghỉ phép năm

Mô tả Công việc

  • Establish, maintain and continuously improve the Laboratory Quality Management System (QMS) in compliance with ISO/IEC 17025:2017, ensuring data integrity, document/record control and validity of test results.
  • Manage QMS documents and records throughout their lifecycle; ensure proper control, traceability, availability and timely updates.
  • Plan and conduct internal audits; manage nonconformities, complaints and CAPA, ensuring root cause analysis and timely closure.
  • Oversee quality control (QC) of laboratory equipment and testing activities; ensure standards, methods and procedures are always up to date with ISO 17025 requirements.
  • Support new test method development and validation, and manage Proficiency Testing (PT) activities, including corrective and improvement actions.
  • Drive innovation and continuous improvement of QMS through digitalization and process optimization, including e-document control, dashboards, automated KPI reporting (Excel/Power BI), and Lean/5S initiatives.

Yêu Cầu Công Việc

- University degree in Analytical Chemistry/Chemistry/Environment/Materials or equivalent

- At least 1-2 year experience in QA/Quality control role, knowledge of Health, Safety & Environmental.

- Experience of working under the ISO/IEC 17025 Quality Management System

- Document/record control; QC data analysis; Excel/SharePoint/LIMS/ AI/ Power BI

- Good writing, reading, speaking and listening skills in English.

Địa điểm làm việc

Hải Phòng
KCN Nam Cầu Kiền, Thủy Nguyên, Hai Phong, Vietnam

Thông tin khác

  • Bằng cấp: Đại học
  • Độ tuổi: Không giới hạn tuổi
  • Lương: Cạnh tranh

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