Clinical Molecular Laboratory Specialist

1 day ago


Tampa, Florida, United States Unified Women's HealthCare Full time
Overview

Florida Woman Care, the largest OB/GYN practice in the state of Florida has built a cutting-edge laboratory in the Tampa area with specialists in GYN Pathology to provide high-quality diagnostic services. We currently have over 250 medical offices and over 600 OBGYN Providers throughout the state of Florida. The Florida Woman Care Laboratory has Histology, GYN Cytology, and Molecular Microbiology capabilities. We are seeking an experienced Clinical Molecular Laboratory Specialist to work in our lab, Monday - Friday, 6:00 AM - 2:30 PM.

The primary responsibilities of this role include performing pre-analytical, analytical, and post-analytical processes associated with specimen processing. This includes participation in documenting and implementing Quality Assurance (QA)/Quality Control (QC)/Quality Inventory (QI) procedures. The successful candidate will also assist in trouble shooting and maintenance of equipment.

Key Responsibilities:

* Perform simple to complex assays utilizing established departmental protocols.
* Read, understand, and adhere to all the SOPs, policies, and protocols.
* Perform all pre-analytical, analytical, and post-analytical testing processes accurately and timely, as well as independently.
* Report results via the Laboratory Information System (LIS).
* Prepare clinical specimens for testing and identify specimen related problems.
* Establish and perform proper quality control measures (i.e. temperature monitoring, instrument maintenance, reagent/specimen preparation, etc.) in accordance with laboratory operating standards.
* Document daily, weekly, monthly, and quarterly quality control (e.g. equipment/instrument maintenance, calibrations, certifications) to support quality assurance initiatives.
* Identify problems that may adversely affect test performance, reporting of test results, or instrument functions. Troubleshoot and/or report findings to supervisor, manager, or director.
* Document all corrective actions taken when test systems deviate from the laboratory's established performance specification.
* Assist the supervisor in ensuring an efficient workflow operation and reports any delays and/or problems.
* Monitor TAT and workflow processes.
* Assist in preparation of validation documentation of new tests and procedures as assigned.
* Maintain records that demonstrate that PT samples are tested in the same manner as patient samples
* Clean and maintain lab equipment, instrumentation, and work space.
* Maintain and track inventory for reagents, consumables, and ancillaries to support laboratory functions. Follow all health and safety regulations when handling laboratory specimens.
* Comply with chemical hygiene and/or laboratory safety procedures.
* Comply with all lab procedures, processes, and methodologies.

Qualifications and Requirements:

* Bachelor's degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution.
* Associate degree in a laboratory science or medical laboratory technology from an accredited institution or equivalent education and training.
* Previous molecular lab experience and/or certification preferred.

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