上海相关职位: 细胞培养技术员/工程师(药厂) 细胞培养技术员/工程师(药厂) 制剂技术员/工程师(药厂) 制剂技术员/工程师(药厂) 制剂技术员/工程师(药厂) 制剂技术员/工程师(药厂) 制剂技术员/工程师(药厂) 制剂研发科学家 制剂研发科学家 分子生物学工程师/助理工程师
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
无工作经验
本科
招1人
11-09 发布
职位描述: Responsibilities/Duties- Perform assigned clinical laboratory testing accurately and in a timely manner.o Resolve pendings. Retrieve and check specimens against pending list. Document specimen discrepancies. Notify laboratory management when specimen discrepancies are not resolved.o Prepare workstation and instrumentation for the assigned testing.o Properly handle specimens and independently resolve technical specimen issues in preparation for analysis and specimen storage. Contact internal customers for clarification as needed.o Operate instruments to perform testing in accordance with established written procedures.o Performs routine testing and calculations as required.o Resolve routine and non-routine assay problems.- Ensure the validity of test results through the performance of established quality assurance and quality control procedures.o Perform experiments, as scheduled, for evaluation of new Calibrator and/or QC lots. Summarize results of investigations and compile data for review by management.o Document quality control results. Interpret quality control results according to Westgard rules or other established departmental procedures, and accurately document biases, warnings, and violations of control rules.o Document corrective action for unusual occurrences (e.g. QC violations, instrument related problems).o Analyze proficiency testing survey samples as patient specimensReagents/Materials/Supplies:- Receive, open and place in service all reagents/materials according to SOPs.- Prepare and properly label reagent, quality control, calibrator material.- Document implementation of new reagents/materials according to SOPs.- Perform parallel testing, linearity’s, stability, other quality control practices needed to ensure validity of material prior to being placed into service.- Perform inventory control of supplies and reagents as approved by management.- Result Entry (Auto-verification and manual entry).- When data is manually entered (e.g. QC, patient data) ensure peer review is performed and documented prior to the release of results.- Prepare proper documentation of test results and enter into the information system.- Generate an appropriate audit trail for all activities.- Document and communicate any result reporting problems or inconsistencies to laboratory management.- Complete testing within the expected turn around time to meet customers’ expectations.- Ensures maintenance of instruments and equipment is performed according to manufacturer and SOP requirements, and documented according to SOP.- Calibrate instruments, equipment, and/or assays as required and document.- Perform basic instrument and equipment troubleshooting.- Perform pipette calibrations and document according to SOP.- Notify laboratory management when an instrument or equipment does not meet specifications.- Comply with regulatory guidelines and Covance Standard Operating Procedures (SOPs) at all times.- Demonstrate proficiency in applicable computer systems and software.- Adheres to established Safety policies and Universal Precaution guidelines at all times. Maintains a clean, organized and safe work environment. Minimizes biohazard waste. Cleans workstation and materials daily.- Takes action for the department when additional responsibilities and opportunities are presented.- Provide laboratory management with a report of activities upon request.- Other duties as assigned.Qualifications- Bachelor’s degree in Medical Technology or Clinical Laboratory Science or other life science with completion of at least a 12-month training program in Medical Technology.- Completed an accredited clinical laboratory training program, or- One year documented laboratory training or experience in the specialty that testing is to be performed.OR- Associate’s degree in medical laboratory technology, experience on genomics testing. PCR, DNA extraction. 职能类别: 生物工程/生物制药 关键字: 医学检测 病理 生化 免疫组化
张江高科技园区李冰路151号 6号楼
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!
质量负责人 20-50万/年
临床项目经理 1.5-2万/月
临床助理研究员 5.5-6.5千/月
企业文化经理 0.8-1万/月
临床数据分析专员 6.5-8.5千/月
研发工程师/研发助理 0.6-1万/月
医学博士 2-2.5万/月
省级销售经理(上海/山东/福建/湖北/广东/云南) 0.6-1.2万/月
临床医学总监 2-2.5万/月
临床监查员(CRA) 5-6千/月
临床项目经理 1-1.5万/月
分子诊断试剂研发工程师 6-8千/月
高级生物信息工程师 1-1.2万/月
研发项目经理 1.5-2万/月
招商经理(体外诊断试剂) 0.6-1.2万/月
上海相关职位: 细胞培养技术员/工程师(药厂) 细胞培养技术员/工程师(药厂) 制剂技术员/工程师(药厂) 制剂技术员/工程师(药厂) 制剂技术员/工程师(药厂) 制剂技术员/工程师(药厂) 制剂技术员/工程师(药厂) 制剂研发科学家 制剂研发科学家 分子生物学工程师/助理工程师
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
