Medical Technologist I (2nd Shift)

Labcorp • Indianapolis, IN, United States • $200k - $250k / year • 1m ago

***$7,500 Sign-on Bonus***

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 60,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives.

We have an exciting opportunity for a Medical Technologist I to join our Genomics Team in Indianapolis, IN!

Scheduled Shift: Monday-Friday 2pm-10:30pm, Saturday Rotation

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. For more detailed information, please click here.

Essential Functions:

Perform assigned clinical laboratory testing accurately and in a timely manner.
Resolve pendings. Retrieve and check specimens against pending list. 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. Contact internal customers for clarification as needed.
Operate instruments to perform testing in accordance with established written procedures.
Perform routine testing and calculations as required.
Resolve routine and non-routine assay problems.
Ensure the validity of test results through the performance of established quality assurance and quality control procedures.
Perform experiments, as scheduled, for evaluation of new Calibrator and/or QC lots. 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. QC violations, instrument-related problems).
Analyze proficiency testing survey samples as patient specimens.
Receive, open, and place in service all reagents/materials according to SOPs.
Prepare and properly label reagent, quality control, calibrator material.
Document implementation of new reagents/materials according to SOPs.
Perform parallel testing, linearity’s, stability, and other quality control practices needed to ensure the validity of material prior to being placed into service.
Perform inventory control of supplies and reagents as approved by management.
When data is manually entered (e.g. QC, patient data) ensure peer review is performed and documented prior to the release of results.
Prepare proper documentation of test results and enter into the information system.
Generate an appropriate audit trail for all activities.
Document and communicate any result reporting problems or inconsistencies to laboratory management.
Complete testing within the expected turnaround time to meet customers’ expectations.
Ensure maintenance of instruments and equipment is performed according to manufacturer and SOP requirements, and documented according to SOP.
Calibrate instruments, equipment, and/or 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.
Maintain a complete up-to-date training file and correct any deficiencies found in the training file.
Ensure training is documented before performing a task.
Successfully complete competency assessments and ensure competency testing documentation is provided to management for review/retention.
Competently perform department duties as set forth in the department training checklist(s).
Assist in training new employees and follow up to ensure training is understood.
Attend department, mandatory, and other meetings and training as required.
Work to achieve partnership with both internal customers and external clients.
Demonstrate proficiency in applicable computer systems and software.
Adhere to established Safety policies and Universal precaution guidelines at all times. Maintain a clean, organized, and safe work environment.
Take 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/Certifications and Licenses:

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.
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.
OR
90 semester hours from an accredited institution that include:
- 16 semester hours of biology courses pertinent to the medical sciences
- 16 semester hours of chemistry (at least 6 semester hours of Inorganic Chemistry)
- 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.
OR
Associate’s degree in medical laboratory technology.

Labcorp is proud to be an Equal Opportunity Employer:

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.

We encourage all to apply

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