Technical Leader (Lab Operation)
费森尤斯医药研发(上海)有限公司
- 公司性质:外资(欧美)
- 公司行业:计算机软件
职位信息
- 发布日期:2017-04-13
- 工作地点:上海-闵行区
- 招聘人数:1人
- 工作经验:5-7年经验
- 学历要求:本科
- 语言要求:英语 熟练
- 职位月薪:1-2万/月
- 职位类别:医药技术研发人员 化学分析测试员
职位描述
职位描述:
Responsible for all the chemical test、packaging materials test、the preparation of reagent、standardization、issuing the C.O.A, inspecting the retention sample, as well as generating specification for new drugs and analytical method validation for new drugs
Main tasks are :
? Confirm to the requirement of regulations and procedure of lab, take charge of physical, chemical and microbial method development, validation/verification and testing of raw materials, intermediate products and finished products, issue the COA/test report, work out the procurement program of reagent and standard. Take charge of the inspection of retained sample and issuing the certificate.
? Ensure Chemist follow the instruction of sampling, testing, recording, calculating, to carry out specific projects according the specification and test method approved and well as QMS procedures and working instructions to carry out the stability study of products, and finish his duty in time.
? Lead specific project on resources allocation, instrument/equipment/working tool planning, reagents/consumables/accessories planning, task execution and corresponding status tracking, project performance and individual personnel’s performance monitoring, project closing, as well as communicating with co-functional teams (CCS, solution/concentration, DA, RA, etc.)
? Lead and perform OOS, OOT and OOE investigations as well as initiate non-conformity report, change control, CAPA, execute CAPA as approved.
? Close team work with support product development as well as product sustaining groups to facilitate project progress.
? Create and/or compile high quality analytical procedure, tech package or SOP, instructions, best practice as required.
? Maintain the instrument, equipment, working tools and facility to make them in a good conditions routinely.
? Ensure the chemists, engineers working in conformance with GMP or 5S concept, company policy, SOPs, and safety regulations.
? Co-ordinate external partners to complete the testing in a timely manner from technical perspective.
? Identify and introduce new analytical technologies, new techniques/equipment and modify equipment or procedures to improve efficiency and productivity.
? Assist laboratory management, includes but not limited to metrology management, material management.
? Make the purchasing plan of reagents and consumable for laboratories and specific projects as needed.
? Inform the superior immediately when OOS test results occurs. To carry out investigation when needed.
? Use the related facilities according the security procedure, improve professional abilities and skills.
? Create specification, test methods, and perform analytical method development, validation/verification for raw materials, packaging materials, intermediates, components and finished products promptly.
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Responsible for all the chemical test、packaging materials test、the preparation of reagent、standardization、issuing the C.O.A, inspecting the retention sample, as well as generating specification for new drugs and analytical method validation for new drugs
Main tasks are :
? Confirm to the requirement of regulations and procedure of lab, take charge of physical, chemical and microbial method development, validation/verification and testing of raw materials, intermediate products and finished products, issue the COA/test report, work out the procurement program of reagent and standard. Take charge of the inspection of retained sample and issuing the certificate.
? Ensure Chemist follow the instruction of sampling, testing, recording, calculating, to carry out specific projects according the specification and test method approved and well as QMS procedures and working instructions to carry out the stability study of products, and finish his duty in time.
? Lead specific project on resources allocation, instrument/equipment/working tool planning, reagents/consumables/accessories planning, task execution and corresponding status tracking, project performance and individual personnel’s performance monitoring, project closing, as well as communicating with co-functional teams (CCS, solution/concentration, DA, RA, etc.)
? Lead and perform OOS, OOT and OOE investigations as well as initiate non-conformity report, change control, CAPA, execute CAPA as approved.
? Close team work with support product development as well as product sustaining groups to facilitate project progress.
? Create and/or compile high quality analytical procedure, tech package or SOP, instructions, best practice as required.
? Maintain the instrument, equipment, working tools and facility to make them in a good conditions routinely.
? Ensure the chemists, engineers working in conformance with GMP or 5S concept, company policy, SOPs, and safety regulations.
? Co-ordinate external partners to complete the testing in a timely manner from technical perspective.
? Identify and introduce new analytical technologies, new techniques/equipment and modify equipment or procedures to improve efficiency and productivity.
? Assist laboratory management, includes but not limited to metrology management, material management.
? Make the purchasing plan of reagents and consumable for laboratories and specific projects as needed.
? Inform the superior immediately when OOS test results occurs. To carry out investigation when needed.
? Use the related facilities according the security procedure, improve professional abilities and skills.
? Create specification, test methods, and perform analytical method development, validation/verification for raw materials, packaging materials, intermediates, components and finished products promptly.
职能类别: 医药技术研发人员 化学分析测试员
公司介绍
费森尤斯医药研发(上海)有限公司诚聘
联系方式
- 公司地址:地址:span田林路1036号绿洲科技三期15号楼