公司行业： 医药/生物工程
公司类型： 外商独资
公司规模： 100-499人
公司简介：
京维通博际是中国第一家拥有符合欧美GLP临床前毒理学服务能力的外商独资医药研发外包组织(CRO)。也是中国唯一一家拥有从药物发现到可同时在美国食品药品管理局(FDA)和欧洲药品管理局(EMEA)备案的临床前医药研发的CRO。公司占地7800平方米，通过了AAALAC认证，也是中国最大最完善的动物实验机构之一。
康龙化成（北京）新药技术有限公司是于2004年成立的美国独资企业，是中国CRO行业北方地区最大的药物研发服务机构，公司以“提升客户药物研发效率”为宗旨，利用尖端组合化学和现代药物化学的核心技术，主营业务为组合化学、药物化学、有机合成化学、化学工艺研发、分析化学、药物筛选、生物制药、药理代谢、病理毒理等新药研发临床前的各个环节。拥有一流的设施和国际顶尖的科研管理团队，通过了AAALAC多物种认证，符合GLP标准，员工总数已经超过700人，其中博士、硕士比例累计超过51%。
2010年1月11日康龙化成收购维通博际成为中国第一家提供从药物发现到申报临床试验新药备案全流程服务的综合性医药研发外包组织，能够给客户提供更完善和全面的药物实验服务，公司将有更大更广阔的发展空间。发展中的公司有更多的职位、发展空间以及具备非常全面和完善的流程化培训体系，并期待着有理想和抱负的新人员加入。
招聘岗位：
1.临床病理（检验）实验室技术人员Clinical Pathology Technician
招聘人数：2-3
职位描述/要求：
临床病理（检验）实验室技术人员
岗位职责：
临床检验实验室主要从事GLP实验中血液、尿液及骨髓标本的检验及分析。
任职要求：
临床检验专业本科或兽医学、 兽医病理学、 兽医病理学与病理生理学硕士；
有临床检验实验室工作经验优先；
熟练操作计算机能
良好的英语交流及读写能力；
优秀的团队精神、工作踏实，具有较强事业心。
Clinical Pathology Technician
The Clinical Pathology Tech provides services to animal toxicology studies by examining and analyzing biological fluids in support of preclinical research and development projects. He/she is responsible for assisting in all aspects of clinical pathology and be supervised by the head of clinical pathology to process specimens for clinical pathology evaluation.
Responsibilities will include
Operate the instruments including Advia 2120 hematology system, clinitek Atlas automated urine chemistry analyzer, Hitachi 7080 serum chemistry analyzer and ACL 9000 coagulation system and relevant instruments to analyze specimens.
Prepare the blood smear and bone marrow smear and have ability in methanol fixative and Wright-Giemsa stain.
Participate in reports on serum chemistry, coagulation, urinalysis and hematology findings.
Maintain legible permanent record of all results obtained together with supporting data.
Ensure all job assignments are performed in compliance with GLP regulations.
Qualifications and Experience
Veterinarian MS in biological science or Clinical pathology related field BS
Experience in animal pathology is preferred
Experience in pharmaceutical industry and GLP requirements
Verbal and written communications skills
Experience in handling biological samples
2. 组织病理学和临床病理学实验室技术人员
招聘人数：2-3
职位描述/要求：
岗位职责：组织病理学实验室主要从事GLP实验中组织切片的制备。
任职要求：
病理学、兽医学、实验动物医学或医学专业本科或硕士；
有病理技术工作经验优先；
熟练操作计算机能力；
良好的英语读写能力；
优秀的团队精神、工作踏实，具有较强事业心。
Histopathology Technicians
participate in the technical aspects of cell and tissue-based visualization assays in support of preclinical research and development projects. They will assist the pathologist and be supervised by the head of histopathology to process histological slides for histopathologic evaluations.
Responsibilities will include
Identify tissues preserved in formalin solution and trim the preserved tissues for histopathology slides.
Prepare paraffin tissue blocks and handle the microtone instrumentation during slide preparation. Will also involve in the handling of instrumentation for dehydration and staining.
Frozen tissue sectioning
Immunostaining and conjugation of antibodies an and proteins with biotin and/or dyes
Microscopy and digital imaging
Ensure all job assignments are performed in compliance with GLP regulations
Qualifications and Experience
BS or MS in biological science, preferably molecular and cell biology or biochemistry
Experience in histology/pathology laboratory work with animal models is preferred
Previous experience with immunofluorescence and multi-target detection methodologies preferred
Must be able to work in small group setting
3. 毒理技术员Associate I, Toxicology
招聘人数：2-3
职位描述/要求：
毒理学—生物学技术员将按照药品非临床研究质量管理规范（GLP）标准进行动物研究和实验室试验，为药物研究与开发提供支持。辅助课题负责人进行毒理学和药理学的研究，并进行跨部门合作。
岗位职责：
动物的保定、观察、给药（口服或静脉注射）、称重及安乐死
理解并遵循课题方案和操作手册
遵守GLP对于文件的要求，包括数据记录，审核纠正等
记录观察数据，识别偏差，明确操作流程，及时向主管汇报并做好记录
及时向课题负责人报告任何课题方案的偏离或意外结果
参与课题方案和总结报告的起草
任职要求：
医学，生物学或者兽医本科及以上学历
有动物实验相关经验优先考虑
The Associate I Toxicology 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 will assist the study director in the conduct of toxicology studies.
Responsibilities will include:
Comprehend and follow study protocols and SOPs for GLP / Non-GLP studies.
Comply with GLP documentation requirements, including data recording, reviewing and correcting.
Animal handling, observation, dosing, blood withdrawing, weighing, necropsy, anesthesia, and euthanization.
Record observations and collect other relevant data via data acquisition system and hand-generated forms.
Report to Study Directors in a timely manner regarding any deviations from protocols or unexpected results.
Contribute to quality control the raw data from studies.
Requirements:
•B.S degree in medicine, biology or veterinary medicine
Work experience in related fields preferred
Basic lab skills are required.
4.毒理技术员Associate III, Toxicology
招聘人数：3-5
职位描述/要求：
Associate III, Toxicology Responsibilities will include
Follow study protocols and SOPs for GLP/ Non-GLP studies.
Contribute to protocol drafting, study preparation, quality control study data and final report drafting.
Contribute to SOP drafting and revising.
Provantis training, problem solving for end users, system libraries maintenance.
Review data, identify potential problems and resolve problems.
Recognize deviations from normal situations, document appropriately, resolve problems with area of expertise, and informs supervisor when the problems are out of their scope.
Train and instruct less experienced staff
Animal handling, observation, dosing, blood withdrawing, weighing, necropsy, anesthesia, and euthanization.
Record observations and collect other relevant data via data acquisition system and hand-generated forms.
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, some degree of training, education or working experience in the US is preferred
Relevant experience in a pharmaceutical, biotech or research organizations and contract toxicology experience is desirable
Excellent computer, communication and writing skills
Good command of English
5. 配药制剂技术人员 Formulation analyst
招聘人数：1-2
职位描述/要求：
Description:
Conduct routine formulation preparations and developments for oral and parenteral dosage forms to support in vivo pharmacokinetics, toxicology and pharmacology studies.
Operate/maintain the on-site HPLC/UV systems, and develop/validate analytical method for formulation analysis.
Perform data record and analysis, generate study protocols and reports in English.
Effectively interact and communicate within a dynamic team environment.
Support test article logistic and formulation procedures in GLP practice environment.
Requirements:
The ideal candidate should possess a B.S./M.S. in pharmaceutical sciences/pharmacy/analytical chemistry with 0-5 years of experience. Experience with formulation preparation, pharmaceutical analysis for small molecules are highly desirable. Demonstrated ability to work independently and in a team environment, and excellent written and verbal communication and good computer skills are required. A candidate with a good understanding about GLP regulations is preferred. Knowledge of pharmacokinetics and drug metabolism in drug research and development are desirable, but not required.
6. 生物分析技术员Associate II, Analysis and Bioanalysis
招聘人数：1-2
职位描述/要求：
The Associate II, Analysis and Bioanalysis, will assist in method validation per FDA guidance, implementing and maintaining analytical and bioanalytical assays and automated systems to support preclinical analytical and bioanalytical studies. The Associate II, Analysis and Bioanalysis, must maintain GLP compliance in supporting preclinical studies and accurately document all work. This Associate II, Analysis and Bioanalysis, will report to the DMPK Technical Supervisor.
Responsibilities will include:
Conduct dose formulation analysis (stability, homogeneity and concentration verification).
Develop and validate analytical and bioanalytical methods with various analytical techniques [LC/MS/MS, LC/UV (DAD or VWD), fluorescence and radioactive detectors].
Conduct sample preparation and extraction such as protein precipitation, liquid-liquid extraction and solid-phase extraction in biological fluids and tissues.
Conduct PK/TK sample analysis and PK/TK and PK/TK analysis with modeling software.
Design, conduct, analyze and report in-life animal PK and bioanalytical studies.
Take the responsibility for operation, maintenance and trouble-shooting of analytical instruments.
Write up the experimental summary report.
Comply with all applicable GLP requirements.
Work either individually or in an interdisciplinary team and possess excellent communication and interpersonal skills.
Design, conduct, analyze and report in-life animal PK and bioanalytical studies.
Qualifications:
M.S. or Ph. D. in the analytical chemistry or related fields
At least 2-year experience of LC-MS/MS.
Having project director experience is desired.
联系方式：
公司名称：北京维通博际医药研发有限公司
公司地址：北京市昌平区科学园路32号
公司主页：ww***com[点击查看] or www.
招聘信箱：hr@ or recruitment@
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