职位描述
生化分析免疫检验临床检验生物化学检验
Job Overview
Responsible for performing a variety of technical procedures and experimental execution in support of sample analysis and validation. Responsible for root cause analysis, troubleshooting, and supporting process improvements.
Essential Functions
● Responsible for performing and documenting analytical procedures in accordance with company procedures and regulatory guidelines.
● Assists in troubleshooting and process improvements to increase data quality, lower costs, or reduce turnaround times to include, updating standard procedures, assisting with troubleshooting.
● Acts as a technical resource for laboratory staff and support the team in the absence of the line manager.
● Performs routine data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances.
● Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel.
● Prepares data analysis results for upload to LIMS system under the guidance of senior level staff.
● Contributes to CAPA investigations, deviations, and resolution.
● Responsible for clear, accurate, and timely communications with cross functional stakeholders.
● Assists in maintaining laboratory equipment and may offer suggestions for new equipment.
● Assists in good housekeeping of the lab environment, consistent with 6S standards.
● Assists in maintaining adequate inventory.
● Responsible for preparation of buffers and solutions for analysis, as required.
● Performs and documents calibration and maintenance of laboratory equipment as assigned.
● Performs and documents hands on training for other lab personnel in areas of proven competency as assigned.
● Participates in continuing education through self-study, attending training sessions and lectures and meetings.
● May lead a laboratory or cross functional projects and assist with implementation of changes.
● May be responsible for contributing to the design and development execution of routine methods/assays under moderate supervision.
● Supports safety, quality, and 6S requirements and initiatives.
● Complies with company's procedures and applicable regulatory requirements.
Qualifications
● Bachelor's Degree Bachelors Degree Or equivalent combination of education and experience (Some CAP/CLIA lab locations may require a BSc in in a chemical, physical, biological or clinical laboratory science,
medical laboratory technology or cytotechnology.) Req
● Typically requires >2 of experience. Req
● Minimum 1 year of experience in a regulated laboratory environment preferred. Pref
● Sound knowledge of principles, theories, and concepts in job area.
● Working knowledge of any applicable regulatory standards within area of responsibility.
● Proficiency with relevant laboratory techniques.
● Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling ,
● Strong technical knowledge of complex testing procedures and science supporting the analysis.
● Proficiency with complex laboratory calculations regarding batches and specimens.
● Ability to troubleshoot laboratory equipment and resolve process issues.
● Good computer skills including proficiency with Microsoft Excel, PowerPoint and Word.
● Effective organizational and interpersonal skills.
● Effective communication and presentation skills.
● Capable of handling multiple tasks simultaneously.
● Strong attention to detail and accuracy.
● Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Responsible for performing a variety of technical procedures and experimental execution in support of sample analysis and validation. Responsible for root cause analysis, troubleshooting, and supporting process improvements.
Essential Functions
● Responsible for performing and documenting analytical procedures in accordance with company procedures and regulatory guidelines.
● Assists in troubleshooting and process improvements to increase data quality, lower costs, or reduce turnaround times to include, updating standard procedures, assisting with troubleshooting.
● Acts as a technical resource for laboratory staff and support the team in the absence of the line manager.
● Performs routine data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances.
● Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel.
● Prepares data analysis results for upload to LIMS system under the guidance of senior level staff.
● Contributes to CAPA investigations, deviations, and resolution.
● Responsible for clear, accurate, and timely communications with cross functional stakeholders.
● Assists in maintaining laboratory equipment and may offer suggestions for new equipment.
● Assists in good housekeeping of the lab environment, consistent with 6S standards.
● Assists in maintaining adequate inventory.
● Responsible for preparation of buffers and solutions for analysis, as required.
● Performs and documents calibration and maintenance of laboratory equipment as assigned.
● Performs and documents hands on training for other lab personnel in areas of proven competency as assigned.
● Participates in continuing education through self-study, attending training sessions and lectures and meetings.
● May lead a laboratory or cross functional projects and assist with implementation of changes.
● May be responsible for contributing to the design and development execution of routine methods/assays under moderate supervision.
● Supports safety, quality, and 6S requirements and initiatives.
● Complies with company's procedures and applicable regulatory requirements.
Qualifications
● Bachelor's Degree Bachelors Degree Or equivalent combination of education and experience (Some CAP/CLIA lab locations may require a BSc in in a chemical, physical, biological or clinical laboratory science,
medical laboratory technology or cytotechnology.) Req
● Typically requires >2 of experience. Req
● Minimum 1 year of experience in a regulated laboratory environment preferred. Pref
● Sound knowledge of principles, theories, and concepts in job area.
● Working knowledge of any applicable regulatory standards within area of responsibility.
● Proficiency with relevant laboratory techniques.
● Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling ,
● Strong technical knowledge of complex testing procedures and science supporting the analysis.
● Proficiency with complex laboratory calculations regarding batches and specimens.
● Ability to troubleshoot laboratory equipment and resolve process issues.
● Good computer skills including proficiency with Microsoft Excel, PowerPoint and Word.
● Effective organizational and interpersonal skills.
● Effective communication and presentation skills.
● Capable of handling multiple tasks simultaneously.
● Strong attention to detail and accuracy.
● Ability to establish and maintain effective working relationships with coworkers, managers and clients.
工作地点
北京大兴区大族企业湾

公司信息
公司介绍
IQVIA(纽交所代码:IQV)是全球专注生命科学领域的高阶分析、技术解决方案和临床研究服务供应商。IQVIA利用深入分析、前沿技术、大数据资源和广泛领域的专业知识,智能连接医疗生态的各个环节。IQVIA Connected Intelligence™快速敏锐地为客户提供强大的数据洞察,帮助客户加速创新医疗的临床开发和商业化进程,以更好的医疗成果惠及患者。IQVIA拥有约72,000名员工,足迹遍布100多个国家/地区。IQVIA拥有多元化的加强型隐私技术和保障手段,能够在保护个人隐私的同时对信息进行管理和分析,帮助医疗利益相关方有效开展精准疗法,获得更佳的疗效。这些洞见和能力能够帮助生物科技、医疗器械、制药公司、医学研究者、政府机关、支付方以及其他医疗利益相关方,获得对疾病、人类行为和科技进步更深入的理解,共同朝着治愈各类疾病的方向迈进。
工商信息
企业名称 艾昆纬医药科技(上海)有限公司
企业类型 有限责任公司(外国法人独资)
法人代表 BRIAN ZIHOU MI
经营状态 存续
成立时间 2013-07-12
注册资本 200万美元
认证资质
营业执照信息

更新于 5月25日







