Clinical Laboratory Scientist

Exer Medical Corporation•Sherman Oaks, CA

23h•Onsite

About The Position

The laboratory scientist is responsible for performance of patient testing to be inclusive of pre-analytical, analytical and post-analytical phases of testing. The scientist must demonstrate minimum qualifications as set forth by CLIA’88 and outlined in “Education and Experience” section below. A Clinical Laboratory Scientist executes a range of standardized microscopic, molecular, chemical and bacteriological tests. They also counsel Providers on pre-test requirements and answer questions related to testing. Clinical Laboratory Scientists also assess the validity of a result that is obtained, preserves proper records of the results, and finalize reporting of results. Make sure that the testing method used follows established quality control procedure and assists with the preparation of laboratory reports. A Clinical Laboratory Scientist organizes and maintains reagents and equipment. They perform maintenance on equipment in the laboratory and keep laboratory in clean and organized condition. Clinical Laboratory Scientist makes use of the laboratory information (LIS) systems to place testing data, generate reports of testing results and search for test results for physicians. Established protocols and procedures are provided and will be followed by laboratory scientists for assurance of safety and quality of patient care.

Requirements

Current license issued by the state of California for Laboratory scientist (Medical Technologist), as generalist or special license for any of the laboratory’s sub-specialties such as molecular.
In-depth knowledge of molecular platforms and laboratory quality control best practices
Minimum of a bachelor’s degree in medical technology
Minimum of one (1) year experience is high complexity laboratory.
At least six (6) months direct hands-on bench work in area or specialty for which he/she is being recruited.
Advance knowledge in area or specialty for which he/she is being recruited.
Problem-solving skills to troubleshoot equipment issues and determine potential causes of inaccurate test results.
Fluent written and spoken English language.
Ability to closely read instructions; Advanced ability in understanding Standard Operating Procedures general protocols.
Attention to detail
Ability to set up and carry out quality control programs for laboratory operations.
Ability to set up, use, and maintain laboratory equipment.
Ability to prepare technical reports, records, and papers related to the work & specialty.
Ability to work efficiently with current laboratory equipment & resources.
Exceptional problem-solving and critical-thinking skills; and ability to provide recommendations(s) to laboratory technical supervisor to improve test conditions & efficiency.
Ability to lift objects not exceeding 20 pounds.
Ability to multitask
Ability to follow biohazard guidelines
Scientist MUST be able to keep his/her State of California license active and current.
Scientists employed by ECL require a high degree of independence and/or leadership; able to work independently in an efficient and within the requirements State & federal compliance laws and guidelines.

Nice To Haves

ASCP certification is recommended but not mandatory requirement.

Responsibilities

Performance of patient testing to be inclusive of pre-analytical, analytical and post-analytical phases of testing.
Execute a range of standardized microscopic, molecular, chemical and bacteriological tests.
Counsel Providers on pre-test requirements and answer questions related to testing.
Assess the validity of a result that is obtained, preserves proper records of the results, and finalize reporting of results.
Ensure that the testing method used follows established quality control procedure.
Assist with the preparation of laboratory reports.
Organize and maintain reagents and equipment.
Perform maintenance on equipment in the laboratory and keep laboratory in clean and organized condition.
Make use of the laboratory information (LIS) systems to place testing data, generate reports of testing results and search for test results for physicians.
Follow established protocols and procedures for assurance of safety and quality of patient care.
Read procedures and completing required training before performing any procedures or protocols.
Ensure the confidentiality of patient information throughout all phases of laboratory testing.
Ensure that specimens are matched to order requisitions.
Ensure that the procedure manual is complete and updated, when necessary, inclusive of but not limited to changes in testing procedures, instruments, and methodology.
Maintain an adequate supply of all reagents and consumables to perform quality testing.
Date reagents and supplies upon receipt.
Periodic monitoring of inventory for expiration dates in cooperation with administrative staff.
Discard expired reagents and supplies and assuring that expired items are not employed for patient testing.
Perform and document on instrument log sheets or in LIS all routine daily, weekly, monthly, and periodic maintenance and function checks following established manufacturers and laboratory protocol.
Perform calibration and calibration verification following established manufacturers and laboratory protocols.
Perform Quality Control as required by the manufacturer and established protocols in laboratory policy.
Identify problems that may adversely affect patient test results.
Apply corrective action steps and/or notifying the Technical Consultant/supervisor or Laboratory Director of issues.
Perform Proficiency Testing and/or Split Sample analysis periodically as outlined in laboratory protocol.
Ensure the Retention of records of all analytic activities performed according to policies and procedures.
Report patient test results by either electronic transmission from interfaced instruments or by manual entry into LIS.
Verify accuracy of test results prior to releasing reports.
Verify critical values by repeat analysis, if possible.
Report critical values to the physician or specified nurse and recording & reporting information action on the appropriate log or in the LIS.
Correct detected reporting errors by following the established protocol.
Perform all Quality Assessment activities assigned to this position and documenting these activities for periodic review by the Laboratory Technical Supervisor/consultant and/or the Laboratory Director.
Retain records of training & competency evaluations provided for inspector’s review, all patient reports, errors, notifications, and corrective actions according to laboratory policies.