QC Manager
25-35万元/年
泰州市
刷新时间:2024-06-12
职位描述
职责描述:
1. To monitor the activities of individual areas of working i.e. Raw Material, Packaging material, GLP activities.
2. To ensure GLP and GMP compliance in every area of working in the laboratory as per written down procedures.
3. To ensure the upkeep of Laboratory instruments, ie, Calibration and Maintenance as per a planned schedule.
4. To ensure proper and timely training of all QC personnel as per the training planner / schedule.
5. To approve all Specifications, Standard test procedures, General test procedures, departmental SOP’s.
6. To ensure timely analytical support to, Production, R&D and Process development.
7. To ensure timely submissions of complete and compliant documents to Quality Assurance and Regulatory.
8. To ensure availability of all required chemicals, columns and any other miscellaneous items and their approval for procurement.
9. To do effective Laboratory investigation in case of OOS/OOT.
10. To ensure timely Analytical technology transfer and Analytical method Validations.
11. Timely review of Departmental SOP’s and compliance of all SOP’s.
12. To ensure Analyst Qualification.
13. To improve and monitor Productivity in Raw material, Packaging Material, GLP sections.
14. To initiate and implement all relevant measures towards CFR part II compliances.
任职要求:
1. Bachelor degree or above, major in pharmacy or related
2. English can be used as the working language
3. Be familiar with QC system processes
其他要求
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1人
- QC总监/QC经理/QC主管
公司介绍
诗迈医药猎头是一家专业从事医药行业猎头服务的科技型企业,总部位于杭州,下属有上海、南京、广州、武汉等多家分公司,同时自主开发国内领先的猎头办公系统及医药人才网站,全面致力于海内外制药、生物、医疗、器械等行业线上线下人力资源整合。
公司与全国各地研发企业、生产企业及销售经营等企业及业内同行建立了良好互动平台,在欧、美、日等国家建立了海归引进平台,同时积极开展医药高等院校公益系列讲座,搭建了以人力、企业为主体的立体化咨询服务网,为医药企业人才队伍建设发挥了积极重要作用,为很多医药企业解决了高端人力之困。