R&D Chemist
江苏费森尤斯医药用品有限公司
- 公司规模:500-1000人
- 公司性质:外资(欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2014-05-29
- 工作地点:常熟
- 招聘人数:1
- 工作经验:三年以上
- 学历要求:本科
- 语言要求:英语精通
- 职位月薪:面议
- 职位类别:化学分析测试员
职位描述
Position Summary工作摘要:
Responsible for all the chemical test, packaging materials test, the preparation of reagent, standardization, inspecting the stability study sample, as well as chemical analytical method validation for new drugs.
负责研发工作范围内的所有化学检验、包装材料的检测、试剂的配制和标定、样品的稳定性考察。还负责新药化学分析方法的验证。
Responsibilities/ Authorities工作职责权限:
1.Confirm to the requirement of regulations and procedure of lab, take charge of physical and chemical test of raw materials、intermediate products and finished products of registered samples used for R&D, work out the procurement program of reagent and standard. Take charge of the inspection of stability study sample.
遵守公司各项管理制度及化验室管理规程;负责进厂研发用的原辅料,包装材料,注册样品半成品和最终产品的物理化学检查;负责制定试剂和标准品的采购计划;负责产品的稳定性考察工作;
2.Chemist should following the instruction of sampling, testing, recording, calculating, to carry out the test according the specification and test method approved, to carry out the stability study for products, and finish his duty in time.
在工作中必须严格按照有关质量检验标准进行取样、检验、记录、计算或判定等,按照标准操作规程操作,对样品进行检验,对本厂留样产品按规定定期取样进行检查,及时完成检验任务;
3.Responsible to prepare the standard solution and all kinds of reagent solutions, and re-standardizing according to the relative procedure.
负责配制检验用的各类试液、标准溶液及其标化和复标,并定期复标;
4.Inform the superior immediately when OOS test results occurs. To carry out investigation when needed.
发现不合格的项目和样品及时汇报,协助有关部门进行调查处理;
5.Use the related facilities according the security procedure, improve professional abilities and skills.
按时完成检验任务,按规程使用化验室设施等,学习新的分析方法和新技术,提高工作技能;
6.Perform analytical method validation for new drug promptly.
及时完成新药开发过程中质量标准方法验证;
Qualifications任职资格:
Education background教育背景:
The personnel shall possess the education, at least college degree of the pharmaceutical or related sciences, master the related chemical knowledge
必须是药学或相关专业大专以上的学历,掌握相关化学检验知识
Work experience工作经验:
least two years’ experiences of related job and have the certain theory knowledge and practical operation skills
至少两年相关工作的经验,具有较强的理论知识和实际操作技能;
Competence and skills技能技巧:
Familiar with the article of GMP, can comply with the requirement of GMP in work and carry out the related SOP.
熟悉GMP条款,并能严格的遵守GMP要求和执行相关的SOP;
Others其它:
Possess of certain computer operating level and professional English level, can read the professional English reference.
具有一定的电脑操作水平和专业英语水平,能流利的阅读本专业的外语参考资料。
Responsible for all the chemical test, packaging materials test, the preparation of reagent, standardization, inspecting the stability study sample, as well as chemical analytical method validation for new drugs.
负责研发工作范围内的所有化学检验、包装材料的检测、试剂的配制和标定、样品的稳定性考察。还负责新药化学分析方法的验证。
Responsibilities/ Authorities工作职责权限:
1.Confirm to the requirement of regulations and procedure of lab, take charge of physical and chemical test of raw materials、intermediate products and finished products of registered samples used for R&D, work out the procurement program of reagent and standard. Take charge of the inspection of stability study sample.
遵守公司各项管理制度及化验室管理规程;负责进厂研发用的原辅料,包装材料,注册样品半成品和最终产品的物理化学检查;负责制定试剂和标准品的采购计划;负责产品的稳定性考察工作;
2.Chemist should following the instruction of sampling, testing, recording, calculating, to carry out the test according the specification and test method approved, to carry out the stability study for products, and finish his duty in time.
在工作中必须严格按照有关质量检验标准进行取样、检验、记录、计算或判定等,按照标准操作规程操作,对样品进行检验,对本厂留样产品按规定定期取样进行检查,及时完成检验任务;
3.Responsible to prepare the standard solution and all kinds of reagent solutions, and re-standardizing according to the relative procedure.
负责配制检验用的各类试液、标准溶液及其标化和复标,并定期复标;
4.Inform the superior immediately when OOS test results occurs. To carry out investigation when needed.
发现不合格的项目和样品及时汇报,协助有关部门进行调查处理;
5.Use the related facilities according the security procedure, improve professional abilities and skills.
按时完成检验任务,按规程使用化验室设施等,学习新的分析方法和新技术,提高工作技能;
6.Perform analytical method validation for new drug promptly.
及时完成新药开发过程中质量标准方法验证;
Qualifications任职资格:
Education background教育背景:
The personnel shall possess the education, at least college degree of the pharmaceutical or related sciences, master the related chemical knowledge
必须是药学或相关专业大专以上的学历,掌握相关化学检验知识
Work experience工作经验:
least two years’ experiences of related job and have the certain theory knowledge and practical operation skills
至少两年相关工作的经验,具有较强的理论知识和实际操作技能;
Competence and skills技能技巧:
Familiar with the article of GMP, can comply with the requirement of GMP in work and carry out the related SOP.
熟悉GMP条款,并能严格的遵守GMP要求和执行相关的SOP;
Others其它:
Possess of certain computer operating level and professional English level, can read the professional English reference.
具有一定的电脑操作水平和专业英语水平,能流利的阅读本专业的外语参考资料。
公司介绍
费森尤斯集团(德国)是一家全球性的医疗保健服务公司,以优质的医疗产品和可信赖的治疗服务享誉全球,是世界五百强企业之一。费森尤斯集团由位于全球范围内的四个独立的事业部组成,包括费森尤斯医疗用品、费森尤斯卡比、费森尤斯赫里奥斯、费森尤斯奥美德。
江苏费森尤斯医药用品有限公司(以下简称“费森尤斯常熟工厂”)隶属于费森尤斯医疗用品,公司成立于2007年7月,是一家集研发和生产功能于一体的企业。公司主要生产用于血液透析的配套产品。现我公司诚邀勤奋敬业、不断超越自我的专业人才加入费森尤斯大家庭!
费森尤斯常熟工厂能为在职员工提供良好的培训与无限的发展空间,同时您也可以在日常工作中领略到多国文化和谐交融的氛围,提高自己的口语水平并拓宽国际视野。另外,公司还为员工提供免费工作餐及常熟市内/苏州班车、年底绩效奖金、带薪年假及其他欧美独资企业所能享有的待遇
江苏费森尤斯医药用品有限公司(以下简称“费森尤斯常熟工厂”)隶属于费森尤斯医疗用品,公司成立于2007年7月,是一家集研发和生产功能于一体的企业。公司主要生产用于血液透析的配套产品。现我公司诚邀勤奋敬业、不断超越自我的专业人才加入费森尤斯大家庭!
费森尤斯常熟工厂能为在职员工提供良好的培训与无限的发展空间,同时您也可以在日常工作中领略到多国文化和谐交融的氛围,提高自己的口语水平并拓宽国际视野。另外,公司还为员工提供免费工作餐及常熟市内/苏州班车、年底绩效奖金、带薪年假及其他欧美独资企业所能享有的待遇
联系方式
- 公司地址:聚富苑民族产业发展基地聚合五街9号