#1: GenSci Pharmaceuticals is looking for VP of foreign registration (570 reads) 作者: caoyanan771124, 时间: 2005-9-09 周五, 10:39 — 作者：游客 在 海归商务 发贴, 来自【海归网】 http://www.haiguinet.com
Company Information
GeneScience (GenSci) Pharmaceuticals Co., Ltd.（www.gensci-china.com）, founded in 1997, is one of the largest bio-pharma with annual sales of about US$20 million in China. The dominant products is GenLei ®；Jintropin®； (Somatropin(rDNA origin) for Injection) which is the leading brand of rhGH in China. The other products in Chinese market are: GenLei ®； Scimax ®； (G-CSF) for neutropenia； GenLei ®； Granmax ®； (GM-CSF) for neutropenia； GenLei ®； Jintrotide ®； (Octreotide) for digestive tract hemorrhage, etc. And GenLei ®； Jintrirelin ®； (Triptorelin) for prostate carcinoma, etc. 10 new products are on pipeline. The proprietary technology contains protein PEGylation, sustain release of biopharmaceutical, E.Coli secretion expression technology and topical and suppository form of bio- pharmaceuticals.
GenSci is aiming to become a global player in endocrine hormone and metabolic disease market. It has one of the largest hGH production facility in the world, product quality surpass EP and USP standard. It has good cGMP compliance and accords with Chinese cGMP and Brazil cGMP. To maintain our dominant position in hGH and take advantage of our quality and cost, GenSci is actively seeking opportunities in registering and exporting GenLei ®；Jintropin®； abroad.
Now we are seeking an individual to be part of our winning team focusing on foreign product registration, especially in US and EU.
Job Description:
Title: VP of foreign registration
Job location: Changchun, China
Type: Full-Time
PhD in Molecular Biology and Protein Chemistry or related in US institution with a minimum of 3 years experience in a US pharmaceutical company or biotech company. Experience in Manufacturing management, QC, preclinical studies and US FDA filing is highly preferred. Responsibilities include preparing, coordinating and compiling information, CMC and preclinical documentation for filings to USFDA or EMEA. Excellent communication skills (both oral and writing) in English and Chinese are required.
We offer a stimulating working environment, a high level of professional and intellectual challenge, and an attractive salaries and comprehensive benefits package. For immediate consideration, Please submit resume to: [email protected].
