Associate Medical Technologist (2nd Shift)

Labcorp Drug Development is looking for an Associate Medical Technologist to join our Targeted Cell Isolation team!

LabCorp Drug Development provides dedicated and fully comprehensive laboratory testing and drug development services to the pharmaceutical industry. We strive to make a difference to people’s everyday lives by bringing essential medicines to the market.

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. 

As a key member of Central Labs team, you will have the following responsibilities (including but not limited to):

Essential Job Duties:

• Perform assigned clinical laboratory testing accurately and in a timely manner, under the supervision of a qualified Technologist.
  • Resolve pending’s. 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.
  • Performs 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, under the supervision of a qualified Technologist.
  • 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 rules.
  • Document corrective action for unusual occurrences (e.g. QC violations, instrument related problems).
  • Analyze proficiency testing survey samples as patient specimens.

• Reagents/Materials/Supplies:
  • 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, 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; performed under the supervision of a qualified Technologist)
  • 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.

• Ensures 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

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. 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

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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