Tổng quan 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.
Kỹ năng chính
Yêu cầu
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
Quyền lợi
Chế độ bảo hiểm Du Lịch Phụ cấp Chế độ thưởng Chăm sóc sức khỏe Đào tạo Tăng lương Nghỉ phép năm
Thông tin bổ sung
QA
Đại học, Kỹ sư, Cambridge Certificate, An Toan Lao Dong
Tiếng Anh, Tieng Thai, Tieng Lao
