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A leading diagnostics laboratory is seeking an Administrative Coordinator for its Quality department in Coppell, TX. This role supports quality assurance activities, compliance audits, and document control, contributing to the lab's regulated environments. Ideal candidates possess relevant experience and a detail-oriented mindset to help ensure high standards of practice.
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Job Details
Level: Experienced
Job Location: IDX Coppell TX Site - Coppell, TX
Position Type: Full Time
Salary Range: Undisclosed
Job Category: Admin - Clerical
Description
About Us
Inform Diagnostics, a Fulgent Genetics Company, is a nationally recognized diagnostics laboratory focused on anatomic pathology subspecialties including gastrointestinal pathology, dermatopathology, urologic pathology, hematopathology, and breast pathology.
Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier, full-service genomic testing company built around a foundational technology platform.
Through our diverse testing menu, Fulgent is focused on transforming patient care in oncology, anatomic pathology, infectious and rare diseases, and reproductive health. We believe that by providing a wide range of effective, flexible testing options in conjunction with best-in-class service and support, we can redefine the way medicine is managed for patients and clinicians alike.
Since integrating with our therapeutic development business, Fulgent is also developing drug candidates for treating a broad range of cancers using a novel nanoencapsulation and targeted therapy platform. By merging our fields of expertise, we aim to become a fully integrated precision medicine company.
Summary of Position
The Administrative Coordinator of the Quality department will assist in supporting projects and activities related to quality assurance, quality improvement, quality audits, document control and other responsibilities. The Administrative Coordinator works closely with all Quality Department teammates and Operations Management team to provide assistance and input into the management and monitoring of the regulated areas of the laboratory. This position may support more than one site, and in addition, will need to work collaboratively with all other company locations with regards to processes such as operating procedures, process improvement and occurrence management.
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