衡阳招聘

职位描述：
Description

We are looking for a Scientist or Sr. Associate Scientist in the field of process development with skillsets and experience in bioreactor operation, and proteins purification, especially for mAB. The candidate will execute cell culture and purification instruments, upstream process development, purification method development and analytical characterization of purified proteins. Scope of work include, but are not limited to, cell culture and purification process development, novel technology development, technology transfer, data analysis and project reporting.
The responsibilities of the candidate will include:
- Evaluate/execute company’s current platforms and technologies in upstream and downstream process development.
- Participate in the technology transfer of bioprocesses internally and externally. The work will i***olve working with commercial and clinical production facilities to ensure accurate technology transfer and successful large-scale production.
- Generate, manage, interpret, and maintain critical data in a highly organized manner; write and present technical reports to management.
- Lead/participate in instrument purchasing and equipment mainte***ce for process development labs.
- Demonstrate effectiveness in collaborative projects in a matrix organization.

Qualifications

A. Education /Training background:

PhD with 0- 3 years related experience, MS with 2- 4 years related experience or BS with more than 5 years of related experience.

B. Knowledge/Skills:

- Experience with developing fed-batch bioreactor processes including optimizing feeding strategies and evaluating different cell culture media and feed formulations.
- Development of robust, scalable, cost effective and well-characterized processes for
 purification of monoclonal antibodies and recombi***t proteins.
- Hands-on experience in chromatography methods and purification systems.
- Experience with microbial fermentation, protein refolding and purification from inclusion body is highly preferred.
- Process optimization, transfer and scale-up into the cGMP manufacturing facilities is preferred.
- Ability to analyze data using statistical tools and to compile technical reports.

C. Others:
- Excellent organizational and planning skills in order to meet deadlines and to handle multi tasks.
- Diligent, self-motivated, independent, strong sense of responsibility.
- Excellent written and verbal communication skills in Chinese and English.
- Good interpersonal skills for building relationships across functions internally and externally.
-Qualified candidates must demonstrate ability to work effectively in multidisciplinary teams.

Primary Location:Asia Pacific-China-Shanghai-Shanghai 举报 分享

公司简介(中文) 恢复为 “成立于1985年的西安杨森制药有限公司（“西安杨森”）是中国***的合资制药企业之一，也是中国改革开放以来进入中国的最早一批制药公司之一，其总部位于北京的中央商业区。西安杨森是强生公司的一员。从创立之初，西安杨森就致力于引进和生产许多创新产品和高质量产品。西安杨森一直致力于投资未来，计划增加在生物制品、心脏病学、风湿病学和泌尿科学领域的新系列产品。西安杨森致力于利用这些新药改善中国患者的医疗保健状况。

本着公司信条和关爱精神，西安杨森一直是活跃的企业公民，在医药、公共卫生、药物研发领域和企业社会责任方面从事了五十多项合作项目。例如，西安杨森与中国卫生部国际卫生交流与合作中心合作创立了“吴阶平医学研究奖和保罗•杨森药学研究奖”，旨在鼓励医药学领域的工作者不断创新。在过去的17年中，共计305名杰出医药学工作者在45个专业领域获得了该奖项，他们在科研领域做出了大量有价值的创新。 此外，西安杨森也被誉为培养制药行业人才的摇篮。1999年，西安杨森被财富杂志（中文版）评选为“中国最受敬仰的十大外资企业之一”。2005年，西安杨森被中国中央电视台评选为“***雇主”，并且分别在2008年、2009年和2010年获得了“中国大学生***雇主奖”。

目前西安杨森所有的招聘信息仅通过前程无忧，智联招聘和猎聘网进行发布，任何在非上述三家招聘网站看到的信息均非西安杨森正式发布。为避免对您的合法权益造成伤害，请务必通过正规渠道投递简历。

2013年，强生在西安高新区投资兴建强生全球供应链先进的生产基地，该项目建设目前已正式启动。新生产基地占地267,000平方米，将取代西安杨森在西安新城区现有的生产基地，成为强生供应链在亚洲的创新枢纽，从而更好地满足中国和其他新兴市场不断增长的需求。新的生产基地将采用世界***的制造技术和先进的质量体系，并引进集电子批号记录和数据存储于一身的全自动化配方生产操作系统以及先进的德国进口生产工艺设备。