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[苏州]百济神州(北京)生物科技有限公司

  1. 发布时间:2020-10-31
  2. 工作地点:其它
  3. 职位类型:全职
  4. 来源:前程无忧(51JOB)
  5. 职位:Formulation R&D (Senior) Scientist 药物制剂研发(高级)研究员
职能类别:大学/大专应届毕业生

职位要求:
1. 硕士或博士学历,药学相关专业。
   Master or Ph.D. degree, major in pharmacy or related field.
2. 具有制剂处方工艺研究经验。
   Experiences on formulation and process development.  
3. 严谨认真,责任心强,良好的团队协作精神和沟通协调能力,以及较强的自主学习能力和抗压能力。
   Rigorous and serious, strong sense of responsibility, good team spirit and communication and coordination ability, as well as strong independent learning ability and ability to work under pressure.
4. 英语水平良好,会熟练使用电脑。
   Good English and good computer skill.
工作职责:
1. 小分子化药新药的制剂处方筛选,工艺研究和优化。
   Formulation development and optimization for new small molecular drugs.
2. 根据项目要求,设计实验方案和项目时间表并按计划完成实验项目。
   According to the requirements of the project, design the experimental protocol and timeline, and complete the development based on the plan.
3. 根据要求完成从小试、中试到正式生产之间的工艺转移和交接。
   According to the requirements, complete the technical transfer and process scle up  from lab R&D, pilot production to formal production.
4. 根据要求,完成相应技术文件的撰写。
   According to the requirements, complete the related technical reports.


公司简要介绍:

公司名称:百济神州(北京)生物科技有限公司
公司类型:上市公司
公司介绍:BeiGene is a global, commercial-stage, research-based biotechnology company focused on molecularly-targeted and immuno-oncology cancer therapeutics. With a team of over 1300 employees in China, the United States, Australia, and Switzerland, BeiGene is advancing a pipeline consisting of novel oral small molecules and monoclonal antibodies for cancer. BeiGene is also working to create combination solutions aimed to have both a meaningful and lasting impact on cancer patients. BeiGene markets ABRAXANE? (nanoparticle albumin–bound paclitaxel), REVLIMID? (lenalidomide), and VIDAZA? (azacitidine) in China under a license from Celgene Corporation.
With fast-growing preclinical and clinical assets in our developing pipeline, there is an immediate need of senior leader with extensive pharmaceutical research and development experiences, particularly in oral solid dose drug product formulation and manufacturing area.


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