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GS药业招聘信息
2012/2/28 7:42:35 | 浏览:1975 | 评论:0

  GS Pharmaceuticals Co., Ltd. , was established in 1996. GS's production facility is located in one of the top 6 national biomedical centers, Changchun High-Tech Development Zone, GS's manufacturing facility covers more than 20,000 sq.m. of land with 11,000 sq.m. of production area. It is one of the largest and best-equipped biopharmaceutical productions in China. As one of the leading genetic engineering pharmaceutical companies in China, GS is also the largest manufacturer of recombinant human growth hormone in Asia. Its branding product - GL® Jp® is the first for recombinant human growth hormone in China. GS has been rapidly growing for 15 years since its foundation, and has become one of the top biopharmaceuticals companies in China.

关于邀请做注射用缓释微球制剂技术的学术带头人的基本要求

  一、掌握注射用缓释微球制剂研发和生产技术,国外相关专业博士毕业并在国外公司已经上市的产品中做过研发或生产;
  二、熟悉FDA关于注射用缓释微球制剂申报要求;
  三、做我公司研发注射用缓释微球制剂技术的学术带头人;
  四、负责解决我公司微球制剂项目的技术难点和相关问题;
  五、可自带项目与金赛合作(蛋白质药物的缓释微球制剂)
  六、可以做全职也可做兼职,1人(待遇面谈)。

    1. Master R&D and production technology of preparation of sustained-release microspheres for injection products, Ph.D. of related profession in foreign universities, with R&D or production experience of launched products in foreign corporations;
    2. Familiar with the FDA’s registration requirements of preparation of sustained-release microspheres for injection;
    3. As the academic leader of preparation of sustained-release microspheres for injection in R&D department;
    4. Responsible for solving technical difficulties and related issues of microspheres preparation project;
    5. Our company can cooperate with you who have preparation of sustained-release microspheres of pharmaceuticals protein products itself;
    6. Full-time or part-time, one person needed (Salary negotiable).

关于邀请做基因工程蛋白质药物的研发学术带头人的基本要求

  一、掌握基因工程蛋白质药物的研发和生产技术,国外相关专业博士毕业并在国外公司已经上市的产品中做过研发或生产;
  二、熟悉FDA关于基因工程蛋白质药物的申报要求;
  三、做我公司研发基因工程蛋白质药物研发的学术带头人;
  四、负责解决我公司基因工程蛋白质药物的研发的技术(发酵、纯化和制剂)难点和相关问题;
  五、可自带项目与金赛合作(基因工程蛋白质药物的仿制和研发)
  六、可以做全职也可做兼职,1到2人(待遇面谈)。

    1. Master R&D and production technology of genetic engineering pharmaceutical protein products, Ph.D. of related profession in foreign universities, with R&D or production experience of launched products in foreign corporations;
    2. Familiar with the FDA’s registration requirements of genetic engineering pharmaceutical protein products;
    3. As the academic leader of genetic engineering pharmaceutical protein products in R&D department;
    4. Responsible for solving technical difficulties(such as fermentation, purification, preparation and etc.) and related issues of genetic engineering pharmaceutical protein products;
    5. Our company can cooperate with you who have genetic engineering pharmaceutical protein products itself;
    6. Full-time or part-time, one or two persons(Salary negotiable).

关于上述两个职位的待遇:

  1、如果做全职年薪不低于50万人民币:免费提供在长春不低于100平方米的住房居住。
  2、如果您在基因工程制药和缓释微球制剂技术领域不仅有实际经验还有学术造诣,我们可推荐您到吉林大学生命科学院任教,同时聘为我公司兼职顾问,待遇另谈。

Salary of the above two positions:

    1. Full-time job:yearly salary is not lower than 500,000 RMB, and provide housing not less than 100 m2 in Changchun for free.
    2. If you have not only practical experience but also scholarly attainments in the field of genetic engineering pharmaceutical and preparation technology of sustained-release microspheres, we can recommend you as a teacher in College of Life Science of Jilin University, concurrently, as a part-time advisor in our company, salary negotiable.

关于国际注册部经理的岗位要求

工作地点:

任职条件:

  • 生物化学、分子生物学、药学或化学等相关专业,硕士及以上学历;
  • 五年以上大型企业海外注册管理工作经验,至少从事过化药制剂产品在欧盟EMEA及美国FDA的申报;熟悉国外新药或仿制药的注册、再注册及补充申请的流程;有过基因工程产品海外注册工作经验者优先;
  • 能够依照ICH相关法规要求,独立完成注册文件(SMF/DMF文件等)的撰写;
  • 能够独立主持国外药政部门的GMP审计工作;
  • 出色的英语书面及口语表达能力,有海外工作商旅经验;
  • 有海外商务发展及专利相关工作背景者优先;
  • 具备较强的领导能力和沟通协调能力;
  • 成熟自信,为人正真,责任感强,有亲和力。

岗位描述:

  • 根据公司产品特点及海外市场注册法规,专利情况和基本市场情况,全面负责公司产品的海外注册策略制定和注册项目规划和管理;
  • 负责公司海外注册及商务合作客户的评估和筛选;
  • 负责组织公司各产品海外注册文件的撰写工作;并对注册资料进行形式和技术审查,以符合申报的需要;
  • 负责主持组织国外药政部门的现场GMP审计工作;
  • 结合海外注册要求,对生产、质保、质检、工艺等相关部门的相关人员进行相关培训;
  • 参与工厂软硬件改造方案的确定;
  • 负责管理,培养公司海外注册团队。

联系单位:吉林省霍普金斯国际药物研究院
联系地址:吉林省长春市贵阳街287号建设大厦20层
邮编:130051
联系电话:0086-431-88018500
传真:0086-431-88018400
手机:0086-18600143450
电子信箱:xye8888@hotmail.com
联 系 人:叶学敏

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