[苏州]爱美津制药公司招聘处方研究员

Company Profile

Amerigen Pharmaceuticals

爱美津制药公司概况

Amerigen is a multinational company with established development and manufacturing platforms aimed at providing high-quality generic pharmaceutical products.

爱美津是一家集研发和制造于一体的跨国公司，旨在向美国提供高质量的仿制药品。

With pharmaceutical assets and science-based expertise in the United States and abroad, Amerigen is able to provide quality products at competitive prices along with unmatched customer service.

凭借在美国和海外的制药资产和技术专家队伍，爱美津致力于提供高品质产品、有竞争力的价格和无以匹敌的客户服务。

At the end of 2007, Amerigen has successfully completed the acquisition of an oral solid dose manufacturing facility in Suzhou, China and established Suzhou Amerigen Pharmaceutical Co., Ltd.

2007年底，爱美津完成了在苏州的口服固体制剂生产厂的收购，并成立了苏州爱美津制药有限公司。

Suzhou Amerigen Pharmaceutical Co., Ltd., located in Suzhou Industrial Park, has successfully passed an US FDA audit in 2010. During this audit, the US FDA confirmed that the facility is capable and has quality systems which can produce pharmaceutical drug products to be exported into commercial commerce in the U.S. market.
苏州爱美津制药有限公司, 位于苏州工业园区，已于2010年成功通过了美国食品药品监督管理局(FDA)的审核。在这次审核中，美国食品药品监督管理局确认了苏州工厂的资质，并认为工厂拥有的质量体系可以使生产的药品销往至美国市场。

Amerigen sincerely welcome you to join its elite staff to build a great generic company.

爱美津真诚欢迎药业精英加盟，共同缔造爱美津的美好未来。

Address: No.58, Qunxing Yi Road, Suzhou Industrial Park

公司地址：苏州工业园区群星一路58号

Main line总机：(86)51267451085

Fax 传真：(86)512 67427891

E-mail邮箱：HR@

1.      Formulation Scientist  处方研究员  1人

Requirements要求:

l        Master degree on Chemical Engineering, Pharmaceutics, pharmacy or   related major.

    化学工程、制剂、药学或相关专业的硕士

l        Good command of written and oral English （Pass CET-6）.

良好的英语口语和书面表达能力。.

Main responsibilities主要职责:

l        Formulation research and development including literature search, study design, experiment execution, result summary, and technical report writing.
处方研究和开发，包括文献检索、研发设计、实验操作和结果汇总和技术报告写作。

l        Develop product manufacturing process and transfer the technology from R&D lab to pilot GMP environment.

将研发实验室的生产工艺转移至GMP中试车间。

l        Work closely with other departments on material sourcing, equipment purchasing, in-process and finished product characterization and drug stability study.

与其他部门紧密合作，确保物料采购、设备采购、中间体和制成品的特性、成品的稳定性研究顺利进行。

l        Support manufacturing process optimization and scale-up, tech transfer and  process validation.  

支持生产工艺的优化、工艺放大、工艺验证和技术转移。

l    Provide project related documents, such as, pharmaceutical development  report, batch record, study protocol and SOP.
支持工艺相关的文件如SOP、批记录、研发方案和药品开发报告。

l    Compliances to the company’s quality systems, FDA cGMPand sFDA GMP regulations and requirements.
符合公司的质量体系要求及美国药监局 cGMP和国内药监局GMP相关的法规要求。