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徠博科 Labcorp · CLS

Clinical Medical Techonologist

薪資面議  /  上海

2025-03-27 更新

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職位屬性

  • 招聘類型:校招
  • 工作性質(zhì):全職

職位描述

Responsibilities / Duties:

Essential Functions

? 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.

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 asset 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.

 

任職條件

Education / Qualifications:

Required:

? 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.