临床病理检验试验室技术人员_实验室检验人员培训
临床病理检验试验室技术人员由刀豆文库小编整理，希望给你工作、学习、生活带来方便，猜你可能喜欢“实验室检验人员培训”。
实验动物饲养与技术人员
实验动物饲养管理人员协助研究人员做饲养管理和一些基本的实验操作。协同其他员工例如兽医的工作人员，技术研究人员和部门经理等。
岗位职责：
日常实验动物的健康检查，喂水喂料，笼具更换清洗等 动物设施设备的清洁卫生 动物的接收运送 正确记录日常活动
工作中符合实验动物相关法规
协同其他员工的工作例如实验技术人员和部门经理等进行相关的实验
任职要求：
动物相关学科专科以上，考虑到工作性质和一定体力要求，优先考虑男性 读懂英文操作规范，英文好的优先 有实验动物抓取保定经验的优先考虑 能吃苦耐劳，身体健康
Animal Care Technician Animal Care Technicians are needed to aist research personnel by performing routine care and handling of laboratory animals and basic research techniques.Animal Care Technicians will interact with a variety of positions including supervisors/managers, veterinarians, technicians and research personnel.Responsibilities will include Daily health checks, feeding, watering, changing/cleaning cages for rodents, rabbits, dogs and primates Sanitize equipment and facilities Receive animal shipments and house animals appropriately Document work accurately Comply with all animal handling and animal welfare regulations and with regulatory
Qualifications and Experience Qualifications and Experience
Certificate of college biology technology or animal science Some animal handling experience Ability to follow written procedures Some lifting required
临床病理（检验）实验室技术人员
岗位职责：
临床病理实验室主要从事GLP实验中血液、尿液及骨髓标本的检验及分析。
岗位要求：
1.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； 2.有临床检验实验室工作经验优先； 3.熟练操作计算机能力
4.良好的英语交流及读写能力；
5.优秀的团队精神、工作踏实，具有较强事业心。
Clinical Pathology Technician – Beijing, PRC 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 aisting in all aspects of clinical pathology and be supervised by the head of clinical pathology to proce 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.1.Prepare the blood smear and bone marrow smear and have ability in methanol fixative and Wright-Giemsa stain.2.Participate in reports on serum chemistry, coagulation, urinalysis and hematology findings.3.Maintain legible permanent record of all results obtained together with supporting data.4.Ensure all job aignments are performed in compliance with GLP regulations.Qualifications and Experience 1.Veterinarian MS in biological science or Clinical pathology related field BS 2.Experience in animal pathology is preferred 3.Experience in pharmaceutical industry and GLP requirements 4.Verbal and written communications skills 5.Experience in handling biological samples
生物分析技术员 I
生物分析技术员I，将在FDA的相关指导下进行临床前期的生物分析和制剂分析研究中样品的提取和分析仪器的维护。生物分析技术员I 应遵循GLP规定，进行规范的数据记录的实验文件保存。该职位向药代动力技术主管汇报。
职位描述：
1.制剂分析（稳定性、均一性和浓度验证）；
2.样品的提取，例如在生物体液和组织中，用蛋白沉淀法、液液萃取、和固相萃取法提取生物样品；
3.负责分析仪器的操作、维护和故障维修； 4.遵守所有相关GLP的要求；
5.能够独立工作并具有团队合作精神，有良好的人际沟通技巧。
任职要求：
1.应具有药代动力学，药学、分析化学或相关领域的大专或本科学位； 2.在生物样品（血浆、组织等）提取方面有0-5年的工作经验。
Aociate I, Analysis and Bioanalysis – Beijing, PRC
The Aociate I, Analysis and Bioanalysis, will aist in sample proceing per FDA guidance, implementing and maintaining analytical and bioanalytical aays and automated systems to support preclinical analytical and bioanalytical studies.The Aociate I, Analysis and Bioanalysis, must maintain GLP compliance in supporting preclinical studies and accurately document all work.This Aociate I, Analysis and Bioanalysis, will report to the DMPK Technical Supervisor.Responsibilities will include:
1.Conduct dose formulation analysis(stability, homogeneity and
concentration verification).2.Conduct sample preparation and extraction such as protein precipitation,liquid-liquid extraction and solid-phase extraction in biological fluids and tiues.3.Take the responsibility for operation, maintenance and trouble-shooting of analytical instruments.4.Comply with all applicable GLP requirements.5.Work either individually or in an interdisciplinary team and poe excellent communication and interpersonal skills.Qualifications: 1.B.S 或Junior college in the pharmacokinetic analysis, pharmaceutical sciences, analytical chemistry or related fields 2.With 0-5 years of experiences of sample proceing for biological samples(plasma, tiues, etc)
配药制剂技术员I Aociate Formulation
主要职责描述：
进行日常性口服和灌胃用药化合物的制剂的准备和配制，以支持对生物体内的药物代谢动力学，毒物学和药理学的相关实验； 执行英文实验数据记录和操作步骤的撰写； 在团队中进行有效的内部协作和沟通；
支持供试药品的管理和保证配药流程符合GLP要求。
任职要求：
应聘者应具有药学，药剂学或者或分析化学大专或本科学位； 具有小分子和大分子（蛋白或多肽）制剂配制者优先考虑； 有相关GLP经验和知识背景的优先；
良好的英语书写和口语沟通能力及熟练的计算机操作能力。
Main Responsibility Description Conduct routine formulation preparations and developments for oral and parenteral dosage forms to support in vivo pharmacokinetics, toxicology and 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 practice environment.Requirements the ideal candidate should poe at least college diploma in pharmaceutical sciences/pharmacy/analytical chemistry with 0-5 years of experience.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 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.Aociate I, Pharmacology The Aociate I Pharmacology will collect, document, 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 with appropriate SOPs, GLPs.He or she will aist the study director in the conduct of pharmacology and safety pharmacology studies.Responsibilities will include:
1.Comprehend and follow study protocols and SOPs for GLP / Non-GLP studies.2.Comply with GLP documentation requirements, including data recording, reviewing and correcting.3.Animal handling, observation, dosing, blood withdrawing, weighing, necropsy, anesthesia, euthanization, surgery and measurement of ECG, respiratory function and CNS FOB and test, etc.4.Record observations and collect other relevant data via data acquisition system and hand-generated forms.5.Report to technical supervisor or Study Director in a timely manner regarding any deviations from protocols or unexpected results.6.Contribute to quality control the raw data from studies.Requirements:
1.B.S degree in life science or diploma in life science with strong animal work and /or surgery skills 2.Work experience in related fields preferred 3.Basic lab and animal work skills are required.组织病理学实验室技术人员
组织病理学实验室主要从事GLP实验中组织切片的制备。
职位要求：
1.病理学、兽医学、实验动物医学或医学专业本科或硕士； 2.有病理技术工作经验优先； 3.熟练操作计算机能力； 4.良好的英语读写能力；
5.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 tiue-based visualization aays in support of preclinical research and development projects.They will aist the pathologist and be supervised by the head of histopathology to proce histological slides for histopathologic evaluations.Responsibilities will include 1.Identify tiues preserved in formalin solution and trim the preserved tiues for histopathology slides.2.Prepare paraffin tiue blocks and handle the microtone instrumentation during slide preparation.3.Will also involve in the handling of instrumentation for dehydration and staining.4.Frozen tiue sectioning
5.Immunostaining and conjugation of antibodies an and proteins with biotin and/or dyes
6.Microscopy and digital imaging
7.Ensure all job aignments are performed in compliance with GLP regulations
Qualifications and Experience 1.BS or MS in biological science, preferably molecular and cell biology or biochemistry
2.Experience in histology/pathology laboratory work with animal models is preferred
3.Previous experience with immunofluorescence and multi-target detection methodologies preferred
4.Must be able to work in small group setting
Pharmacologist /Aociate III, Pharmacology– Beijing, PRC
The Pharmacologist or Aociate III, pharmacology will adhere to Pharmaron SOPs, comply with GLP, ICH and other guidelines and maintain the highest standards to ensure the integrity 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 will include but not limited to: 1.Development of various disease models and technical procedures for study purposes.2.Act as study director for pharmacology, safety pharmacology and related safety studies.3.Provide data and analysis for study reports 4.Prepare study protocols and study reports Qualifications and Experience: 1.MS or PhD in life sciences
2.Experience in animal ECG or surgery preferred 3.Knowledge of regulatory requirements 4.Able to use English for work activities
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