1.审核Audit:进行过程审核与跟进纠正措施。To carry out process audit and follow-up of corrective actions.
2.产品审核Product Audit:根据质量目录(QK)和检验单进行产品审核。跟进纠正措施。Product audit as per Quality catalogue (QK) and inspection sheets. Follow-up of corrective actions.
3.设备操作和管理 Equipment Operation and Handling:负责测量设备的操作和维护。To operate and maintain the measuring equipment under the responsibility.
4.仓库和原材料储存审核。Warehouse and Raw material storage Audit;仓库审核如审核计划与跟进纠正措施。Warehouse audit as per audit plans and follow-up of corrective actions
5.玻管和托盘的检验。Inspection of Tubing and Pallets.
6.包装材料检验Inspection of Packing material,创建检查单。根据检验指导书提出不符合项问题单。Create Inspection check sheet. Raise non-compliance-issue-sheet as per inspection instruction
7.访问客户现场了解问题Visit customer site for Issues ,创建观察/分析报告Create observation/analysis report
8.确保符合TC程序、T要求、ISO 9001、ISO 15378(GMP)。Ensure compliance to TC procedures, T requirements, ISO 9001, ISO 15378 (GMP).
9.积极参与持续改进活动,领导改进。Active participation in continuous Improvement activities and leading improvements.
10.遵循管理层定义的本地和全球愿景和价值观。Follow Local and Global Vision and Values defined by Management.
11.遵循部门程序和文件,以符合ISO体系、GMP、精益和EHS。Follow departmental procedures and documentation to comply with ISO Systems, GMP, Lean & EHS.
12.管理层(上级)随时指派的任何其他职责/职能。Any other duties/ functions assigned from time to time by the management (Superiors)
任职要求:
1.正规教育和培训Formal Education and Training: 技术专业教育Technical professional education
2.职业经验Occupational Experience: 机械或技术背景,2-3年工作经验,如有质量控制经验,在玻璃行业/制药行业有经验。mechanical or technical background with 2 to 3 years experience and if possible experience in Quality control with if possible experience in the in glass industry / pharmaceutical industry.
3.附加知识要求Additional Knowledge Requirements: 具备英语、校准、现行ISO 9001要求、逻辑思维、系统工作能力和解决问题的能力。Should have knowledge of English, Calibration, current ISO 9001 requirements, logical thinking, systematic working skills and skills in problem solving.
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