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             海口维瑅瑷（VTI）生物研究院是由美国疫苗技术有限公司（Vaccine Technologies Incorporation，VTI）投资，于2005年3月在海口注册成立的一家高端生物技术研发机构。该院位于海南省海口市秀英区长怡路20号，占地30亩，由美籍华人科学家吕亦晨教授担任法人代表和首席科学家，主要从事艾滋病疫苗、治疗性乙肝疫苗和新型流感疫苗以及HIV、HBV、EBV和HPV等的细胞免疫检测试剂盒的研发工作。此外，还承接国际资助的科学培训项目和举办有关的国际学术交流活动。

            海口维瑅瑷（VTI）生物研究院的技术平台是一种基于分子生物学和生物信息学的全新的疫苗构建技术。从疫苗设计到生产的整个过程中，无需借助任何病毒，从根本上避免了传统疫苗研制中有可能造成的生物污染问题。

二、所在地区：海南省海口市秀英区长怡路20号

三、企业性质：外商独资

四、企业人数：50-60

五、联系方式：电话：0898-68713972或 0898－68717682；       传真：0898-68717682

电子邮件：hr@vaccinetechnologies.com

联系人：  刘小姐或 吴小姐

 

ÿ    Strong  English  communication  skills  are  essential  and  CET-6  certificate  is  required.

ÿ    MS with 5 years experience in protein chemistry to supervise and assist in GMP    pilot purification runs of E. Coli paste containing recombinant proteins to be used as vaccine candidates in clinical trials.

ÿ    Knowledge of AKTA Explorer for small scale purification development is required.

ÿ    Must be well versed in large scale column chromatography such as affinity, ion   exchange.

 

 

We are looking for scientists to join our Eukaryotic Protein group.  The group is responsible for the production of recombinant proteins under GMP conditions using a baculovirus based expression system. This is an opportunity for qualified candidates to get in on ground floor of process development and GMP manufacturing in support of the company's clinical and large scale production efforts.  The successful candidates will be responsible for the development and implementation of large scale culturing techniques and protein production.

ÿ      The role requires a BS/MS degree in Biotechnology, Cell Biology, Biochemistry or related field with a minimum of 5 years experience in the pharmaceutical or biotechnology industry. 

ÿ      Candidates with previous managerial experience are preferred.

ÿ      Large scale, insect cell culture experience is a must. 

ÿ      Experience with bioreactor and BioWave operation and maintenance is a plus.

ÿ      Expertise in protein purification using the AKTA FPLC system is also preferable. 

ÿ      The candidates should have a track record of problem solving, good organization and communication skills and the ability to collaborate within multidisciplinary teams.

 

We are looking for someone to lead in the development and management of a range of immunoassay clinical diagnostic kits.  This person will be responsible for the implementation and direction of investigative projects at the production facility and at the clinical sites. They will be required to travel to the clinical sites to monitor the studies and coordinate investigations.  Generate oral and written reports as necessary.

ÿ      Minimum BA/BS in biology or science related field with 2 - 6 years experience in developing immunoassays. 

ÿ      Preference will be given to candidates with skills and knowledge of clinical study design and FDA regulations. 

ÿ      Experience in flow based immunoassays is a plus. 

ÿ      Previous management experience is preferred and QC experience is a plus.

ÿ      Must be able to travel. 

 

 

GMP文件的起草、发放等工作；

ÿ      监控生产、检验用仪器设备按照GMP管理规范进行购置、验收、安装运行与验证，监控计量仪器校验执行；

ÿ      物料的现场监督；

ÿ      GMP文件的中英文互译。

1、英语达到CET-6水平，熟练英语笔译；

2、具有生物医学等相关专业教育背景；

3、本科以上学历；

4、熟练操作计算机；

5、男性优先   。

                   

   负责产品申报、制定方案、监督协调整个项目进度

   1、具有医学、药学或生物学教育背景

2、熟悉药品管理法，药品注册管理办法；

3、诚实可靠、吃苦耐劳。

1、专业不限，具有药学、医学、生物学教育背景的优先考虑；

2、熟练操作电脑；

3、英语能力达到CET-4以上；

4、有相关工作经验者优先。

 

七、其他事项：待遇面议。

请投递中英文简历到信箱：hr@vaccinetechnologies.com

                                             海口维瑅瑷生物研究院