北京维通博际医药研发有限公司是一家在中国从事非临床研究的外商独资企业。公司致力于非临床研究领域，建立的初衷是在中国建立世界一流的非临床研究实验室，并且在亚洲从事符合美国FDA, GLP标准的实验研究。
下面是公司简介和招聘职位信息：
Bridge Laboratories
北京维通博际医药研发有限公司
Headquartered in Maryland, Bridge Laboratories is a company focused on high-quality and cost-effective preclinical drug development services in the US and China for the pharmaceutical and biotechnology industries. Bridge recently acquired Gene Logic Laboratories. The combined company has more than 300 employees, and the capabilities now include nearly all aspects of US/EU/JP regulatory compliant preclinical drug discovery and development services.
Bridge recently opened a state-of-the-art animal vivarium in China in the prestigious Zhongguancun Life Sciences Park in Beijing. This facility was designed from the ground up to US accreditation standards, and operates under US-level GLP standards.
Bridge is a globally integrated (China- and US-focused) preclinical CRO with US level state-of-the-art facilities; AAALAC and US-level animal welfare protection; validated software and data acquisition; strict data security and encryption; global customs and shipping logistics; quality animal supply; US-level quality assurance training and compliance; project management, US board certified pathology services, English-only SOPs together with a motivated; client-centric, and highly trained and experienced staff.
Please visit ww***com[点击查看] for further information. If the national firewall blocks the US site, Please try ww***.ca[点击查看]
Welcome the most energetic, excellent ones to join us for drug development in China.
公司地址：昌平区科学园路32号，中关村生命科学园区内
邮政编码：102206
电子邮箱：hr@ or hr@
招聘职位信息：
1. Toxicologist - Beijing, PRC
The Toxicologist II will collect, document, and manage pertinent data including animal observations, test material administration, and clinical sample collection in compliance with appropriate SOPs, GLPs. He or she may serve as study director in the conduct of toxicology studies.
Responsibilities:
· Follow study protocols and SOPs
· Report to Study Directors in a timely manner regarding any deviations from protocols or unexpected results
· Contribute to protocol drafting, study preparation, quality control study data and final report drafting.
· May contribute to SOP drafting and revising.
· Provantis training, problem solving for end users, system libraries maintenance.
· Recognize deviations, determine course of action, including notifying supervisor and document appropriately.
· Review data and identify potential problems
· Train and instruct less experienced staff
· May serve as Study Director in the conduct of toxicology studies.
Requirements:
· Master’s or PhD degree (PhD preferred) in medicine, biology or veterinary medicine
· Work experience in related fields preferred
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