Molecular Technologist I responsibilities include, but are not limited to, the following:Follow standard operating procedure for specimen handling and processing, test analyses, and maintain accurate documentation for specimen traceability.Adhere to established policies and procedures whenever test systems are not within acceptable performance levels.Document all corrective actions taken when test systems deviate from established performance specifications.After initial training, perform assigned Lab Assistant Duties and TEM-PCR lab duties accurately and efficiently, including properly handling equipment.  These duties may include Sample Sorting, Spin, Decap and Batch, Sample Transfer, Template Addition, Elution Plate Prep, PCR Product Addition, SAPE Addition, Array Wash, Array Detection, and other duties as assigned.Stock laboratory with supplies in addition to clean and decontaminate laboratory instruments and testing areas.Setup and perform testing of samples for troubleshooting, clinical, and stability studies.Setup and assist with validation and verification studies of laboratory tests.Properly document records of studies performed, assuring traceability.QC DutiesAdhere to all processes put into place by the Quality Assurance and Safety Officer.Promptly bring forth all QC concerns to a Lead or Technical Supervisor.Contribute when needed in processing QC Samples.All AreasPerform all work duties as assigned by shift on weekly work schedules, using any downtime for lab maintenance or other assigned duties.Adhere to the laboratory's quality control policies and document all quality control activities.Be capable of identifying problems that may adversely affect test performance or reporting of test results and correct the problem or immediately notify the day’s lead technologist.Participate in the laboratory’s quality assurance plan.Participate in job specific training and annual competency assessment reviews.Keep workstations clean according to the cleaning policy.Wear personal protective equipment as required.Observe all safety guidelines and report any unsafe conditions to a lab supervisor or manager.Perform any additional duties as directed by Clinical Lab management.
Job Details
ID | #53126615 |
Estado | Kentucky |
Ciudad | Louisville |
Tipo de trabajo | Full-time |
Fuente | Eurofins |
Showed | 2024-12-20 |
Fecha | 2024-12-20 |
Fecha tope | 2025-02-18 |
Categoría | Etcétera |
Crear un currículum vítae |
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