Job
Description
You will be responsible for performing clinical laboratory flow cytometry analysis accurately and in a timely manner. This includes resolving pendings, checking specimens against pending lists, documenting specimen discrepancies, and notifying laboratory management when discrepancies are not resolved. You will also be required to perform routine testing, calculations, and resolve both routine and non-routine assay problems. Ensuring the validity of test results is crucial, and you will do so by following established quality assurance and quality control procedures. This involves conducting experiments for the evaluation of new Calibrator and/or QC lots, summarizing investigation results, compiling data for management review, and documenting quality control results. You will also be responsible for interpreting quality control results according to departmental procedures, documenting biases, warnings, and violations of control values, as well as documenting corrective actions for unusual occurrences. Result entry, both through auto-verification and manual entry, is part of your responsibilities. When manually entering data, such as QC and patient data, peer review must be performed and documented before releasing results. Proper documentation of test results must be prepared and entered into the information system, along with generating an appropriate audit trail for all activities. Any result reporting problems or inconsistencies should be documented and communicated to laboratory management promptly. Compliance with regulatory guidelines and Covance Standard Operating Procedures (SOPs) is mandatory. You will be in charge of maintaining an up-to-date training file, ensuring completion of required training before task performance, and passing competency assessments as scheduled. Training new employees may also be part of your duties, along with attending department meetings and mandatory training sessions as per the training matrices. Establishing partnerships with internal customers and external clients is essential. This involves pulling data for review, providing accurate responses to audit findings, resolving issues collaboratively, responding to customer inquiries promptly, and understanding department metrics and goals. Proficiency in computer systems and software relevant to the role is expected. Maintaining a clean, organized, and safe work environment is crucial for ensuring smooth operations. You should be proactive in taking on additional responsibilities and opportunities presented by the department. Providing laboratory management with activity reports upon request and performing any other duties assigned are also part of your role. The ideal candidate should hold a Medical Technologist (CFC holder) or Pharmaceutical Biology Technologist (CFC holder) qualification, or equivalent degrees from recognized institutions. Labcorp is an Equal Opportunity Employer and encourages candidates of all backgrounds to apply. If you require assistance due to a disability, please visit Labcorp Accessibility for support. For information on data privacy, refer to our Privacy Statement.,
