上海招聘

职位描述：
Job Major Accountabilities岗位主要职责
?Responsible for the routine QC work including sampling, in-process control, finished product release.
?Responsible for the establishment, execution of method validation project.
?Support the R&D and stability sample testing
?Responsibility for daily maintenance of lab equipment and environment
?Handle routine quality system investigation procedure in operation process such as OOS, Deviation, and CAPA.
?Establish and review the Lab documents such as SOP, Protocol, validation reports.
?Strictly follow the SOPs and EHS rule of company
?Other task as assigned by superior

Basic Requirements主要任职条件
?College degree or above. Majored in medicine analysis or related with laboratory and industry experience for 2-3 years
?Basic knowledge of pH, UV, IEF, SDS-PAGE, etc.
?The experience of GMP environment or pharmaceutical company
?Good communication, cooperation and organization skills
?Computer Literate MS Office to include Excel and Word
?Working as part of a team or alone/remotely

CORE COMPETENCE 核心竞争力
?Knowledge in medicine analysis or Pharmaceutical laboratory and industry experience
?Teamwork spirit and Self-motivated
?Good communication and trouble shooting

 Major Contacts(Outside Organization) 主要接触对象 (公司以外)
Internal: Quality Assurance, Engineering , Manufacture, Purchase, Logistic
External: Vendor


CRITICAL SUCCESS FACTORS关键考核/成功指标：
?The quantity and quality of QC bench work
?The quantity and quality of documentation 举报 分享

    2009年12月8日，上海复星医药新药研究有限公司与美国汉霖生物技术公司正式签约合资组建上海复宏汉霖生物技术公司，致力于单克隆抗体药物的研发与产业化。公司位于上海市漕河泾新兴技术开发区，注册资本3000万美元。 复宏汉霖主要致力于应用前沿技术进行单克隆抗体药物的开发及商业化，造福更多病患。 目前公司正在开发的产品主要覆盖肿瘤、自身免疫性疾病等领域。公司以全球联动整合创新为产品开发的理念，在中国上海、美国加州和台北均设有研发实验室，配备了单抗药物前期研发所需的符合国际化标准的各项仪器设备，其中上海实验室总面积约3,000 平方米，目前在建中的实验室面积约10,000平方米。现已完成单克隆抗体药物开发平台的建设。另外，复宏汉霖率先向国内引进了先进的一次性生产技术，进行单抗产品GMP生产。借助该项优势技术，复宏汉霖现已实现5年5个产品、5项适应症IND申报的高效研发，位于同行业领先地位。展望未来，复宏汉霖人将始终以“开发优质抗体药物，造福全球病患”为使命，不断探索创新，努力耕耘，积极打造深得信赖，领先中国进而影响全球的生物制药企业。
    复宏汉霖矢志成为国内领先、国际一流的生物制药公司。而人才是公司成功的最重要的根基与动力。

         期待您的加盟！


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