Clinical Laboratory Scientist I, II, III - Tues-Sat 9:30am-6pm

Eurofins•Lenexa, KS

About The Position

Transplant Genomics Inc. (TGI), a molecular diagnostics company within Eurofins, develops non-invasive biomarker testing to monitor transplant outcomes. Its portfolio includes 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, troubleshooting, equipment calibration, and quality control procedures. The role is responsible for ensuring valid test results with a high level of proficiency and in accordance with Eurofins Transplant Genomics standard operating procedures. The position is scheduled Tuesday through Saturday, 9:30 a.m. to 6 p.m.

Requirements

Bachelor of Science or Bachelor of Arts degree in biological, physical, chemical, or clinical laboratory science.
Authorization to work indefinitely in the United States without restriction or sponsorship.
Willingness to work with potentially infectious human blood and body fluids.
Ability to work with automated and manual platforms.
Skills in aseptic techniques.
Intermediate proficiency with PC-based software programs.
High integrity and honesty in performing tests, documenting results, and maintaining patient, client, employee, and laboratory business confidentiality.
Excellent verbal and written communication skills.
Analytical judgment, problem-solving skills, accuracy, and 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.
Level I: Comfort with raw specimen handling.
Level I: Ability to read, interpret, and comply with internal SOPs, operating and maintenance instructions, and company policies.
Level I: Intermediate proficiency with PC-based software programs.
Level II: Meet Level I qualifications and have at least 2 years of clinical laboratory experience at CLS Level I work or in a CLIA-certified laboratory overseen by a Clinical and/or Medical Director in a regulated environment.
Level II: Demonstrate superior understanding of departmental processes and ensure applicable SOPs are used and followed appropriately.
Level III: Meet Level II qualifications and have at least 6 years of clinical or CLIA-certified laboratory experience overseen by a Clinical and/or Medical Director in a regulated environment.
Physical dexterity to use hands, arms, and shoulders repetitively to operate a keyboard and other office equipment, use a telephone, and access cabinets and items at various levels, including overhead.
Ability to speak and hear clearly enough to communicate 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 information, 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 inventory of supplies, reagents, and materials needed for testing.
Document remedial action, 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 appropriately 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 with other laboratory associates to complete daily activities efficiently.
Represent the department and organization in accordance with company standards and associate attributes.
Perform other duties as assigned by management.
For Level II, orient, mentor, and teach clinical laboratory methods, procedures, and techniques to new associates; share knowledge; perform formally assigned additional 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 assigned train-the-trainer and Qualified Personnel responsibilities.