
Medical Technologist III- Special Chemitry

職位描述
Essential Functions
? Instruments/Equipment: o Demonstrates thorough working knowledge of instruments/equipment in the department.
Able to provide troubleshooting guidance to staff to resolve complex instrument and equipment problems. Works with the vendor where needed to resolve instrument/ equipment related problems and summarize results of investigations.
? Training: o Coordinates the timely development and completion of training materials and checklists.
o Seeks and promotes expertise in department and across sites to ensure consistent approach to training.
? SOP: o Initiates revisions to SOPs or writes new SOPs to reflect current processes that ensure compliance. Coordinates with other departments and other sites to ensure timely completion of SOP. Resolves obstacles, where needed.
? Instrument/Equipment/Assay Validation o Responsible for coordinating with other resources to ensure timely completion and implementation of new assay validations.
o May be asked to research, develop, validate and maintain procedures in area of responsibility and make recommendations on modification/improvement of procedures to management.
? Process Improvement: o Able to analyze existing processes and create new approaches or ideas to improve. Works with internal/external department to ensure successful implementation of changes
/improvements.
o Demonstrates extensive knowledge of all department functions, and may serve as subject matter expert for department on company wide initiatives (i.e., Six Sigma).
Supports client audit process and responding to inquiries.
? Serves as an expert in all facets of trained workstations in area of responsibility. Responds to problems or questions of department staff.
Non-Essential Functions
? Only individuals that are verified to qualify as supervisory personnel under regulations/standards applicable to the facility (e.g., New York State, CLIA, CAP) may perform periodic review and approval of quality control program records (e.g. quality control data, instrument logs, reagent logs). The SOPs applicable to the department should be consulted to determine records that can be reviewed and approved.
任職要求:
Required:
? Individual must qualify as testing personnel under MoH regulations.
Preferred:
? Bachelor's degree in Medical Technology or completion of at least a 12-month training program in Medical Technology.
OR
? Bachelor's degree in a chemical, physical or biological science from an accredited college or university and one year training and/or experience in the specialty in which testing is to be performed. Such training must be equivalent to that received in a school of Medical Technology.
Working experiences:
Individual must have 3 or more years of Covance Laboratory experience performing clinical laboratory testing or experience in performing clinical laboratory testing judged as equivalent.
企業簡介
科文斯,全球性的合同研究組織(CRO)Covance Inc.是全球服務最全面的藥物研發公司。
我們致力于推動醫療保健事業發展并實現Solutions Made Real?,通過向制藥公司和生物科技公司提供高質量的非臨床、臨床前試驗、臨床和商業化服務,幫助減少藥物研發的時間和成本。憑借豐富的經驗與深厚知識,我們具備獨特的優勢,能為客戶合作伙伴提供不僅僅局限于測試的獨到見解。
我們還向化學品、農用化學品和食品行業提供實驗室測試服務,同時也是毒理學分析服務、中心實驗室服務、藥物篩選服務的市場領導者,以及III期臨床試驗管理服務的全球頂級提供商。
科文斯官網: https://www.covance.com/
職位發布企業

科文斯醫藥研發(北京)有限公司上海分公司
企業性質:外資企業
企業規模:5000-10000人
成立年份:2006
企業網址:www.covance.com
企業地址:上海市普陀區嵐皋路555號602-606室
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職位發布日期: 2019-04-25