Clinical Laboratory Scientist I, II, III - Tues-Sat, 3PM-11:30PM

Eurofins•Lenexa, KS

About The Position

Transplant Genomics Inc. (TGI), part of Eurofins, is a molecular diagnostics company focused on improving organ transplant outcomes through non-invasive serial monitoring guided by biomarkers. Its products include whole-blood gene-expression and donor-derived cell-free DNA testing for kidney transplant patients, as well as a blood-based biomarker assay for liver transplant patients. The Clinical Laboratory Scientist performs laboratory testing, preventive maintenance, equipment troubleshooting and calibration, and quality-control procedures. The role is responsible for the validity of test results and requires working with a high level of proficiency in accordance with Eurofins Transplant Genomics standard operating procedures. The position is scheduled Tuesday through Saturday, 3:00 PM to 11:30 PM. The posting describes three levels, with progressively greater experience, technical knowledge, training, and participation in laboratory activities.

Requirements

Bachelor of Science or Bachelor of Arts in biological, physical, chemical, or clinical laboratory science.
Authorization to work in the United States indefinitely without restriction or sponsorship.
Willingness to work with potentially infectious human blood and body fluids.
Ability to work with automated and manual platforms.
Skills required for aseptic techniques.
Intermediate proficiency with PC-based software programs.
High integrity and honesty when performing tests, documenting results, and maintaining confidentiality of patient, client, employee, and laboratory business information.
Excellent verbal and written communication skills.
Analytical judgment, problem-solving skills, accuracy, and strong attention to detail.
Level I: At least 1 year of clinical laboratory experience in a CLIA-certified laboratory, overseen by a Clinical and/or Medical Director in a regulated environment.
Level I: Ability to safely handle potentially infectious human blood and body fluids using appropriate personal protective equipment (PPE).
Level I: Comfort with raw specimen handling.
Level I: Ability to read, interpret, and follow internal SOPs, operating and maintenance instructions, and company policies.
Level II: Meets Level I qualifications and has at least 2 years of clinical laboratory experience performing CLS Level I work, or experience in a CLIA-certified laboratory overseen by a Clinical and/or Medical Director in a regulated environment.
Level II: Superior understanding of departmental processes and ability to ensure applicable standard operating procedures are being used and followed appropriately.
Level III: Meets Level II qualifications and has at least 6 years of clinical or CLIA-certified laboratory experience overseen by a Clinical and/or Medical Director in a regulated environment.
Ability to repetitively use hands, arms, and shoulders to operate a keyboard and other office equipment, use a telephone, and access file cabinets and items stored at different heights, including overhead.
Ability to speak and hear well enough to communicate clearly in person, by telephone, and in group settings.
Ability to operate a personal computer continuously for extended periods of 4 or more hours.
Mental acuity to collect and interpret data, evaluate, reason, define problems, establish facts, draw conclusions, and make judgments and decisions.
Must be vaccinated against novel COVID-19 virus variants or provide proof of an approved exemption.

Responsibilities

Examine samples for validity and other requirements, including sample type and volume.
Prepare samples, including accurate and precise specimen pipetting.
Operate, calibrate, and maintain assigned laboratory equipment and instruments according to standard operating procedures.
Prepare reagents and materials for testing.
Maintain adequate inventory of testing supplies, reagents, and materials.
Document remedial actions, troubleshooting, quality assurance activities, and instrument maintenance.
Adhere to established processing timelines.
Enter data into the Laboratory Information Management System (LIMS).
Label samples and deliver them to the appropriate areas.
Retrieve and re-file samples for testing.
Store specimens properly for short-term and long-term storage.
Assist laboratory personnel with cleaning duties.
Follow quality and safety standards and comply with applicable regulatory agencies.
Follow laboratory policies and protocols.
Communicate and work closely with other laboratory associates to complete daily activities efficiently.
Represent the department and organization favorably and in accordance with company standards and associate attributes.
Perform other duties as assigned by management.
Perform laboratory assays according to standard operating procedures.
Accept or reject test results according to standard operating procedures.
For Level II, orient, mentor, and teach clinical laboratory methods, procedures, and techniques to new associates; share knowledge; take on formally assigned duties such as training; and participate in special project teams as requested.
For Level III, participate in troubleshooting with the Technical Supervisor, serve on laboratory or company committees and panels, and perform train-the-trainer and Qualified Personnel responsibilities as assigned.