武汉招聘

Principal Duties and Responsibilities

• Participate in a series of related training (operation training and documentation training).

      参加操作和文件相关的培训。

• Do the preparatory work before the start of the experiment. (e.g.: the preparation of BR, materials, labels, TAR and so on.)

      完成实验前的准备工作（如批记录起草、物料、标签、请检单等）。

• Technology transfer from external part to MSAT.

      工艺到MSAT部门

• Perform the early and late stage process development and troubleshooting

       前期及后期工艺开发和解决疑难

• Process scale up from 200L to manufacturing 2000L.Ensure tasks are completed in accordance with approved site procedures, batch records, and protocols.

      按照批准的规程、批生产记录和方案，完成200L至2000L的工艺放大。

• According to the production process, review and revise the relevant GMP documents.

      生产工艺审阅和修改相关GMP文件。

• Summary change control of owner each project, Optimize and improve processes, improve efficiency.

      总结每个项目的变更控制，并优化和提高生产效率。

• Freezer management. (Including 4℃，-20℃，-80℃ Freezer)

       管理4℃，-20℃，-80℃冰箱

• Cooperate with the teammate to execute protein purification process in accordance with batch record.

      和团队成员一起按照批记录纯化蛋白。

• Make the appropriate experimental records during the experiments.

      试验期间按要求记录试验记录

• Timely completion of qualification and calibration of instruments and equipment.

       及时完成仪器和设备的确认和校准。

Job Requirements

岗位要求

• Master’s Degree in Life Sciences/Chemistry/Pharmacology or Bachelor’s Degree in Life Sciences/Chemistry/Pharmacology and 3+ year of related experience in purification using automated control systems. 

      具备生命科学/化学/药学专业的硕士或具有3年及以上从事相关蛋白纯化工作经验的本科学历。

• Excellent oral and written communication skills in English and Mandarin (Read, Write, Verbal) demonstrated by communicating with other functions and management regarding resolving investigations and theory. 

      优秀的中英文口头和写作能力。

• Thorough knowledge and understanding of biopharmaceutical technology, processes. 

       对生物制药技术、工艺有较深入的知识和认识。

• Must be flexible to work on any shift (day, night, weekend)

      适合弹性的工作时间，愿意配合加班。

• Capable of writing detailed reports and summaries and exhibit detail oriented documentation skills. 

      具备撰写各种总结、报告的能力。

• Familiarity of computer-based systems.

      熟悉电脑操作

鼎康生物是一家领先的CDMO公司，可提供一站式的CMC解决方案，支持从早期药物开发到后期临床研究和商业化cGMP生产。鼎康引进了全球***模块化生物制药工厂Kubio；为客户开发的多个产品已经在全球20多个国家进行临床试验。在不久的将来，鼎康生物总产能将超过140,000L。我们承诺通过技术和生产创新，使全球患者都能负担得起具有国际标准的生物药物，提高治疗水平以改善人类健康。