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

Scheduled Shift: Tuesday-Friday 2pm-10:30pm and Saturday 12pm-8:30pm

Pay Range: 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. 

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.  Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. 

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 as set 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.

Education/Qualifications/Certifications and Licenses

U. S. Requirements

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. Such training must be equivalent to that received in a school of Medical Technology.

OR

· 90 semester hours from an accredited institution that include the following:

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.

OR

· Associate?s degree in medical laboratory technology

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* Experience in Flow Cytometry analysis is preferred but not required.