臨床病理（檢驗）實驗室技術(shù)人員

1、<p>　　實驗動物飼養(yǎng)與技術(shù)人員 </p><p>　　實驗動物飼養(yǎng)管理人員協(xié)助研究人員做飼養(yǎng)管理和一些基本的實驗操作。協(xié)同其他員工例如獸醫(yī)的工作人員，技術(shù)研究人員和部門經(jīng)理等。</p><p><b>　　崗位職責：</b></p><p>　　日常實驗動物的健康檢查，喂水喂料，籠具更換清洗等</p><p&g

2、t;　　動物設施設備的清潔衛(wèi)生</p><p><b>　　動物的接收運送</b></p><p><b>　　正確記錄日?；顒?lt;/b></p><p>　　工作中符合實驗動物相關(guān)法規(guī)</p><p>　　協(xié)同其他員工的工作例如實驗技術(shù)人員和部門經(jīng)理等進行相關(guān)的實驗</p><p

3、><b>　　任職要求：</b></p><p>　　動物相關(guān)學科?？埔陨希紤]到工作性質(zhì)和一定體力要求，優(yōu)先考慮男性</p><p>　　讀懂英文操作規(guī)范，英文好的優(yōu)先</p><p>　　有實驗動物抓取保定經(jīng)驗的優(yōu)先考慮</p><p>　　能吃苦耐勞，身體健康</p><p>　　An

4、imal Care Technician</p><p>　　Animal Care Technicians are needed to assist research personnel by performing routine care and handling of laboratory animals and basic research techniques. Animal Care Technici

5、ans will interact with a variety of positions including supervisors/managers, veterinarians, technicians and research personnel.</p><p>　　Responsibilities will include</p><p>　　Daily health chec

6、ks, feeding, watering, changing/cleaning cages for rodents, rabbits, dogs and primates Sanitize equipment and facilities </p><p>　　Receive animal shipments and house animals appropriately </p><p&g

7、t;　　Document work accurately </p><p>　　Comply with all animal handling and animal welfare regulations and with regulatory </p><p>　　Qualifications and Experience</p><p>　　Qualificat

8、ions and Experience </p><p>　　Certificate of college biology technology or animal science</p><p>　　Some animal handling experience </p><p>　　Ability to follow written procedure

9、s </p><p>　　Some lifting required</p><p>　　臨床病理（檢驗）實驗室技術(shù)人員</p><p><b>　　崗位職責：</b></p><p>　　臨床病理實驗室主要從事GLP實驗中血液、尿液及骨髓標本的檢驗及分析。</p><p><b>　　

10、崗位要求：</b></p><p>　　1.    臨床檢驗專業(yè)本科或獸醫(yī)學、 獸醫(yī)病理學、 獸醫(yī)病理學與病理生理學碩士；</p><p>　　2.    有臨床檢驗實驗室工作經(jīng)驗優(yōu)先；</p><p>　　3.    熟練操作計算機能力</p>&l

11、t;p>　　4.    良好的英語交流及讀寫能力；</p><p>　　5.    優(yōu)秀的團隊精神、工作踏實，具有較強事業(yè)心。</p><p>　　Clinical Pathology Technician – Beijing, PRC</p><p>　　The Clinical Pathology

12、 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 clinica

13、l pathology and be supervised by the head of clinical pathology to process specimens for clinical pathology evaluation.</p><p>　　Responsibilities will include:</p><p>　　Operate the instruments i

14、ncluding 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.</p>&l

15、t;p>　　Prepare the blood smear and bone marrow smear and have ability in methanol fixative and Wright-Giemsa stain.</p><p>　　Participate in reports on serum chemistry, coagulation, urinalysis and hematolog

16、y findings.</p><p>　　Maintain legible permanent record of all results obtained together with supporting data.</p><p>　　Ensure all job assignments are performed in compliance with GLP regulations

17、.</p><p>　　Qualifications and Experience</p><p>　　Veterinarian MS in biological science or Clinical pathology related field BS</p><p>　　Experience in animal pathology is preferred&l

18、t;/p><p>　　Experience in pharmaceutical industry and GLP requirements</p><p>　　Verbal and written communications skills</p><p>　　Experience in handling biological samples</p>&l

19、t;p>　　生物分析技術(shù)員 I </p><p>　　生物分析技術(shù)員I，將在FDA的相關(guān)指導下進行臨床前期的生物分析和制劑分析研究中樣品的提取和分析儀器的維護。生物分析技術(shù)員I 應遵循GLP規(guī)定，進行規(guī)范的數(shù)據(jù)記錄的實驗文件保存。該職位向藥代動力技術(shù)主管匯報。</p><p>　　職位描述：1. 制劑分析（穩(wěn)定性、均一性和濃度驗證）；2. 樣品的提取，例如在生物體液和組織中，用蛋

20、白沉淀法、液液萃取、和固相萃取法提取生物樣品；3. 負責分析儀器的操作、維護和故障維修；4. 遵守所有相關(guān)GLP的要求；5. 能夠獨立工作并具有團隊合作精神，有良好的人際溝通技巧。</p><p>　　任職要求：1.    應具有藥代動力學，藥學、分析化學或相關(guān)領(lǐng)域的大?；虮究茖W位；2.    在生物樣品（血漿、組織等）提取方面有0-5年的工作

21、經(jīng)驗。</p><p>　　Associate I, Analysis and Bioanalysis – Beijing, PRCThe Associate I, Analysis and Bioanalysis, will assist in sample processing per FDA guidance, implementing and maintaining analytical and bio

22、analytical assays and automated systems to support preclinical analytical and bioanalytical studies. The Associate I, Analysis and Bioanalysis, must maintain GLP compliance in supporting preclinical studies and accuratel

23、y document all work. This Associate I, Analysis and Bioanalysis, will report to the DM</p><p><b>　　配藥制劑技術(shù)員I</b></p><p>　　Associate Formulation </p><p>　　主要職責描述：進行日常性口服和

24、灌胃用藥化合物的制劑的準備和配制，以支持對生物體內(nèi)的藥物代謝動力學，毒物學和藥理學的相關(guān)實驗；執(zhí)行英文實驗數(shù)據(jù)記錄和操作步驟的撰寫；在團隊中進行有效的內(nèi)部協(xié)作和溝通；支持供試藥品的管理和保證配藥流程符合GLP要求。</p><p>　　任職要求：應聘者應具有藥學，藥劑學或者或分析化學大?；虮究茖W位；具有小分子和大分子（蛋白或多肽）制劑配制者優(yōu)先考慮；有相關(guān)GLP經(jīng)驗和知識背景的優(yōu)先；良好的英語書寫和

25、口語溝通能力及熟練的計算機操作能力。</p><p>　　Main Responsibility DescriptionConduct routine formulation preparations and developments for oral and parenteral dosage forms to support in vivo pharmacokinetics, toxicology and

26、pharmacology studies.Perform data record and formulation procedure in English. Effectively interact and communicate within a dynamic team environment.Support test article logistic and formulation procedures in GLP pra

27、ctice environment.</p><p>　　Requirementsthe ideal candidate should possess at least college diploma in pharmaceutical sciences/pharmacy/analytical chemistry with 0-5 years of experience. 

28、0;Experience with formulation preparation both for small molecules and protein/peptides are highly desirable. Demonstrated ability to work independently and in a team environment, and excellent written and verbal communi

29、cation and good computer skills are required. A candidate with a good understanding about GLP regulations is preferred. K</p><p>　　Associate I, PharmacologyThe Associate I Pharmacology will collect, documen

30、t, and manage pertinent data including animal observations, test material administration, clinical sample collection, animal surgery and measurement of ECG, respiratory function and CNS FOB and test, etc in compliance wi

31、th appropriate SOPs, GLPs. He or she will assist the study director in the conduct of pharmacology and safety pharmacology studies.  Responsibilities will include: 1. Comprehend and follow study pr</p

32、><p>　　Requirements:</p><p>　　1. B.S degree in life science or diploma in life science with strong animal work and /or surgery skills2. Work experience in related fields preferred3. Basi

33、c lab and animal work skills are required.</p><p>　　組織病理學實驗室技術(shù)人員 </p><p>　　組織病理學實驗室主要從事GLP實驗中組織切片的制備。</p><p>　　職位要求：1.    病理學、獸醫(yī)學、實驗動物醫(yī)學或醫(yī)學專業(yè)本科或碩士；2.  &#

34、160; 有病理技術(shù)工作經(jīng)驗優(yōu)先；3.    熟練操作計算機能力；4.    良好的英語讀寫能力；5.    優(yōu)秀的團隊精神、工作踏實，具有較強事業(yè)心。</p><p>　　Histopathology Technicians participate in the technical aspects of cell a

35、nd 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 histop

36、athologic evaluations. </p><p>　　Responsibilities will include</p><p>　　1. Identify tissues preserved in formalin solution and trim the preserved tissues for histopathology slides. </p>

37、<p>　　2. Prepare paraffin tissue blocks and handle the microtone instrumentation during slide preparation. </p><p>　　3. Will also involve in the handling of instrumentation for dehydration and s

38、taining. </p><p>　　4. Frozen tissue sectioning </p><p>　　5. Immunostaining and conjugation of antibodies an and proteins with biotin and/or dyes </p><p>　　6. Microscopy and

39、 digital imaging </p><p>　　7. Ensure all job assignments are performed in compliance with GLP regulations</p><p>　　Qualifications and Experience</p><p>　　1. BS or MS in biolog

40、ical science, preferably molecular and cell biology or biochemistry </p><p>　　2. Experience in histology/pathology laboratory work with animal models is preferred </p><p>　　3. Previous exp

41、erience with immunofluorescence and multi-target detection methodologies preferred </p><p>　　4. Must be able to work in small group setting</p><p>　　Pharmacologist /Associate III, Pharmacolog

42、y– Beijing, PRC </p><p>　　The Pharmacologist or Associate III, pharmacology will adhere to Pharmaron SOPs, comply with GLP, ICH and other guidelines and maintain the highest standards to ensure the integrity

43、 of preclinical study data. Under the guidance from the Director of Pharmacology, the individual will be responsible for preclinical pharmacology, safety pharmacology and related safety studies. Responsibilities w