武汉招聘

Job Responsibilities

1. Participate in the formulation development/optimization and stability evaluation activities of biopharmaceutical preparations and drug product fill & finish, such as monoclonal antibodies, bispecific antibodies, recombinant proteins, etc.;

   参与生物药物的制剂开发/优化和成品灌装的工艺开发及稳定性评估活动，如单克隆抗体,双特异性抗体,重组蛋白等；

2. Carry out research and development of macromolecular pharmaceutical preparations in accordance with domestic and international drug quality guidelines and GMP requirements;

   根据国内外药物质量要求和GMP要求，进行大分子药物制剂研发；

3. Standardize and make relevant original records in accordance with the requirements, compile and archive materials and write research reports;

   按照要求规范并做好相关的原始记录，进行资料的编写归档并撰写研究报告；

4. Cooperate closely with the work of relevant departments, coordinate project progress and solve related problems;

   紧密配合相关部门的各项工作，协调项目进展并解决相关问题；

5. Other work arranged by superior leaders.

   上级领导安排的其他工作。 

 

Job Requirements

1. Master degree or above in Pharmaceutical Sciences, Biochemistry, Biophysics, Chemistry, Chemical Engineering；

   硕士及以上学历，药学、生物化学、生物物理学、化学、化学工程或相关专业；

2. Have theoretical knowledge and experience with molecular biology, protein chemistry, biochemical characterization of proteins or other biological drugs;

   在分子生物学、蛋白质化学、蛋白质或其他生物药物的生物化学表征方面具有理论知识和经验；

3. Have the following experimental experience in protein characterization and have some understanding of chromatography(HPLC/UPLC) and protein particulates (HIAC/FlowCam or MFI/SLS) monitoring;

   具有如下蛋白质特征分析的实验经历，对色谱（HPLC/UPLC）及蛋白质微粒观测(HIAC/FlowCam or MFI/SLS)有所了解；

4. Active, highly responsible, with team spirit;

   工作积极主动，高度负责，具有团队合作精神；

5. Good oral and written communication skills in Chinese and English.

   良好的中英语读写和沟通能力。

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。