上海相关职位: 药物制剂研究员 销售工程师 药品化学分析技术支持工程师 包材相容性项目工程师 化学品安全技术支持工程师 生物测试工程师 化学实验室能力管理工程师 高级药品质量体系工程师 环境有机分析师 药品微生物分析师
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09
职位描述: The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job. It is the responsibility of each employee to comply with all applicable regulations e.g. Good Clinical Practice, Good Laboratory Practice, Clinical Laboratory Standards Institute, in the performance of their role.Duties and Responsibilities:1.Mainly perform clinical laboratory testing for non-Tox studies (Extraction of Nucleic acid and the QPCR, ELISA determination etc.) accurately and in a timely manner.a)Retrieve and check specimens against pending list. Document and resolve any specimen discrepancies. Notify laboratory management when specimen discrepancies are not resolved.b)Prepare workstation and instrumentation for the assigned testing.c)Receive, open and place in service all reagents according to SOPs.d)Prepare and properly label reagents and document according to SOPs.e)Operate instruments to perform testing in accordance with established written procedures.f)Resolve routine and non-routine assay problems with assistance.g)Process and ship samples according to study specific instructionsh)Evaluates and solves problems related to the collection and processing of specimens.2.Ensure the validity of test results through the performance of established quality control procedures. Interpret quality control results according to established departmental procedures.a)Prepare quality control material accurately.b)Report the quality control results to the management, troubleshoot, and take corrective action on questionable or out-of-limit results. Documents all corrective actions and submits them for review by the management.3.Result Entrya)Prepare proper documentation of test results and enter into the information system.b)Document and report any result reporting problems or inconsistencies to laboratory management.c)Complete testing within the expected turn around time to meet customers’ expectations.4.Perform maintenance on instruments and equipment daily, weekly, monthly, and document.a)Ensure that maintenance is performed and documented according to SOP.b)Perform basic instrument and equipment troubleshooting with assistance.c)Notify laboratory management when an instrument or equipment does not meet specifications.5.Regulatory compliancea)Comply with regulatory guidelines, Universal Precautions and Covance Standard Operating Procedures (SOPs) at all times.6.Demonstrate proficiency in applicable computer systems and software. . Operate and utilize all communications systems available in the laboratory; telephones, copiers, facsimile machines and pagers.7.Participates in proficiency testing and maintains a record of on-going competency along with personal training file.8.Maintain a clean, organized and safe work environment. . Handles hazardous materials, reagents and chemicals in a safe manner according to SOP.9.Exercises and maintains levels of competence, integrity and interpersonal skills necessary to attain regulatory and quality goals.10.Other duties as assignedEducation/Qualifications:?Bachelor degree in Life Sciences, medical laboratory technology or equivalentExperience:?A minimum of 2 year experience as a lab technician I. Or a minimum of 2 year related external experience based on education.?Could accomplish the PCR/QPCR related work independently;?Familiar with the enzyme immunoassay(ELISA) determination.公司地址:上海康新公路3377号 有班车 职能类别: 医药技术研发人员
周浦康新公路3377号
Why Covance? At Covance, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world. We Offer Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. There is no better time to join us!
药品注册经理 1-1.5万/月
销售人员 4-8千/月
生物医药商务总监 1.5-2万/月
医药代表(全市民营医院) (职位编号:FD销003) 0.6-1.2万/月
医务专员/医务代表 6-8千/月
专科产品事业部医药代表 1-1.5万/月
销售经理 15-20万/年
医药代表(上海) 0.8-1万/月
生物实验助理(生物/医学/化学) 3-4.5千/月
实习生(生物/医学/化学)生物科研产品服务 2-4千/月
实习生(销售/推广/渠道)生物/化学/医学相关专业 2-4千/月
生物科研试剂销售工程师 0.6-1万/月
质量经理/Quality Manager-食品/化工/医药/添加剂配料 2.5-3万/月
Quality Auditor/质量审核/供应商审核/体系/FDA-医疗 1-1.5万/月
上海相关职位: 药物制剂研究员 销售工程师 药品化学分析技术支持工程师 包材相容性项目工程师 化学品安全技术支持工程师 生物测试工程师 化学实验室能力管理工程师 高级药品质量体系工程师 环境有机分析师 药品微生物分析师
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09