Medical Technologist I (Flow Cytometry)
Company: Labcorp Careers
Location: Indianapolis
Posted on: September 2, 2024
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Job Description:
Sign-on Bonus $7,500****
In this role, you will be working in our *Indianapolis, IN* office
location within the *Flow Cytometry* Department. Candidate will be
expected to accurately and efficiently perform multiple flow
cytometry setups daily, as well as subsequent data acceptability
checks upon completion of departmental and panel-specific
training.
Working days within the lab are Tuesday-Saturday. Scheduled hours
will be 2nd shift, Tuesday-Friday 2-10:30pm, Saturdays
12pm-8:30pm.
*Benefits:* All job offers will be based on a candidate's skills
and prior relevant experience, applicable degrees/certifications,
as well as internal equity and market data. Regular, full-time or
part-time employees working 20 or more hours per week are eligible
for comprehensive benefits including: Medical, Dental, Vision,
Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time
off (FTO), Commissions, and Company bonus where applicable. Perform
assigned clinical laboratory testing accurately and in a timely
manner.
* Document specimen discrepancies. Notify laboratory management
when specimen discrepancies are not resolved.
* Prepare workstation and instrumentation for the assigned
testing.
* Properly handle specimens and independently resolve technical
specimen issues in preparation for analysis and specimen
storage.
* Operate instruments to perform testing in accordance with
established written procedures.
* Performs routine testing and calculations as required.
* Document and communicate any problems or inconsistencies to
laboratory management.
Ensure the validity of tests results through the performance of
established quality assurance and quality control procedures.
* Summarize results of investigations and compile data for review
by management.
* 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.
* Document corrective action for unusual occurrences (e.g. Analyze
proficiency testing survey samples as patient specimens.
Reagents/Materials/Supplies:
* Receive, open and place in service all reagents and materials
according to SOPs.
* Prepare and properly label reagent, quality control, calibrator
material.
* Document implementation of new reagents and materials according
to SOPs.
* Perform parallel testing, linearity studies, stability studies,
other quality control practices needed to ensure validity of
material prior to being placed into service.
* Perform inventory control of supplies and reagents as approved by
management.
Ensures maintenance of instruments and equipment is performed and
documented according to manufacturer and SOP requirements.
* Calibrate instruments, equipment, and assays as required and
document.
* Perform basic instrument and equipment troubleshooting.
* Perform pipette calibrations and document according to SOP.
* 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
* Individual is responsible for maintaining his/her complete
up-to-date training file and is accountable for correcting any
deficiencies found in his/her training file.
* Individual is responsible for ensuring he/she is trained and
training is documented prior to performing a task.
* Individual can competently perform department duties as set forth
in the department training checklist(s).
* The individual successfully completes, as scheduled, competency
assessments and ensures competency testing documentation is
provided to management for review and retention.
* May assist in training new employees and follows-up to ensure
training is understood.
* Demonstrates proficiency in applicable computer systems and
software.
Adheres to established Safety policies and Universal precaution
guidelines at all times. Cleans workstation and materials
daily.
Provide laboratory management with a report of activities upon
request.
Individual must qualify as testing personnel under the following
CLIA 1988 and New York State Department of Health requirements:
-- Bachelor's degree in Medical Technology or Clinical Laboratory
Science or other life science with completion of at least a
12-month training program in Medical Technology.
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.
1) 16 semester hours of biology courses, which are pertinent to the
medical sciences
2) 16 semester hours of chemistry (at least 6 semester hours of
Inorganic Chemistry)
3) 3 semester hours of math
-- Completed an accredited clinical laboratory training program, or
one year documented laboratory training or experience in the
specialty that testing is to be performed.
Associate's degree in Medical Laboratory Technology
#As an EOE/AA employer, Labcorp strives for diversity and inclusion
in the workforce and does not tolerate harassment or discrimination
of any kind. We make employment decisions based on the needs of our
business and the qualifications of the individual and do not
discriminate based upon race, religion, color, national origin,
gender (including pregnancy or other medical conditions/needs),
family or parental status, marital, civil union or domestic
partnership status, sexual orientation, gender identity, gender
expression, personal appearance, age, veteran status, disability,
genetic information, or any other legally protected characteristic.
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Keywords: Labcorp Careers, Indianapolis , Medical Technologist I (Flow Cytometry), Healthcare , Indianapolis, Indiana
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