
Medical Technologist-Genomics 基因檢測技術員

職位描述
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 tests 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 values.
o Document corrective action for unusual occurrences (e.g. QC violations, instrument related problems).
o Analyze proficiency testing survey samples as patient specimens. ? Reagents/Materials/Supplies:
o Receive, open and place in service all reagents/materials according to SOPs.
o Prepare and properly label reagent, quality control, calibrator material.
o Document implementation of new reagents/materials according to SOPs.
o Perform parallel testing, linearity’s, stability, other quality control practices needed to ensure validity of material prior to being placed into service.
o Perform inventory control of supplies and reagents as approved by management.
? Result Entry (Auto-verification and manual entry).
o When data is manually entered (e.g. QC, patient data) ensure peer review is performed and documented prior to release of results.
o Prepare proper documentation of test results and enter into the information system.
o Generate an appropriate audit trail for all activities.
o Document and communicate any result reporting problems or inconsistencies to laboratory management.
o Complete testing within the expected turnaround time to meet customers’ expectations.
? Ensures maintenance of instruments and equipment is performed according to manufacturer and SOP requirements, and documented according to SOP. o Calibrate instruments, equipment and/or assays as required and document.
o Perform basic instrument and equipment troubleshooting.
o Perform pipette calibrations and document according to SOP.
o 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.
? Training
o Individual is responsible for maintaining his/her complete up-to-date training file and is accountable for correcting and deficiencies found in his/her training file.
o Individual is responsible for ensuring he/she is trained and training is documented prior to performing a task.
o The individual successfully completes, as scheduled, competency assessment and ensures competency testing documentation is provided to management for review/retention.
o Competently performs department duties as set forth in the department training checklist(s).
o May assist in training new employees and follows-up to ensure training is understood.
o Attends, as scheduled, department, mandatory and other meetings and training, as required according to training matrices.
? Work to achieve partnership with both internal customers and external clients by:
o Pull data in a timely manner for review by QA and external clients.
o Contribute to the provision of accurate verbal or written response to internal QA and client audit findings. Coordinate, where needed, with other resources to resolve issue.
o Researches and prepares a response following investigation for quality purposes. Coordinate, where needed, with other resources to resolve issue.
o Research and responds in a timely manner to internal customer inquiries regarding status of test results, retrieval of samples for testing/storage and other needs.
o Understand department metrics and goals.
? 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.
Education / Qualifications
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.
Experience
1 year lab experience, chemistry department prefer.
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