上海招聘

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 instructions
h) 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 Entry
a) 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 compliance
a) 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 assigned

Education/Qualifications:
? Bachelor degree in Life Sciences, medical laboratory technology or equivalent

Experience:
? 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

LabCorp是全球顶尖的生命科学公司，科文斯作为LabCorp旗下的药物研发部门，肩负着改善人类健康与生命的共同使命。科文斯的实验室和设施遍布全球，在世界范围内拥有超过26000名员工，卓越的研发能力和强大的人才资源奠定科文斯在医药研发行业的领先地位。截止到2020年，科文斯中国团队共参与了近100个获得上市许可的新药研发，积极支持超过50个免疫肿瘤药物的研发项目，是服务***面的药物研发公司。

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