Molecular Technologist III

Benefits

Additional Information

Molecular Technologist III Include but are not Limited to the Following: The Molecular Technologist III is responsible for specimen labeling, processing, test performance and storage, lab maintenance, supply stocking, logging temperature and lot numbers, aliquoting reagents, and following standard lab procedures, safety guidelines, and HIPAA policies. The position is also responsible for processing samples with molecular technologies other than TEMPCR, such as qPCR Technical Duties 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 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. Other laboratory tasks that will be performed once trained are Sample Correction, Stool Extraction, Array Plate Building and Proplate Pressing. Stock laboratory with supplies in addition to cleaning and decontaminating 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. Advanced Technical Duties After initial training, perform assigned qPCR lab duties accurately and efficiently including properly handling qPCR equipment. Proper handling of instrument blocks for qPCR equipment. PCR Reagent Prep Extraction and Hybridization Reagent Prep QC Duties Adhere 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 Areas Perform 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. Additional Job Considerations A day's schedule can be affected by specimen delivery delays, possibly resulting in later arrival times or later finish times. Flexibility with scheduling, within reason, is required. Weekend and holiday work is required. Work during adverse weather conditions, as much as safety will allow, is required. Lab work requires a majority of time standing or walking and dexterity with hand-eye coordination. Basic computer skills are required. Must comply with CLIA or any other medical requirements to work in the laboratory Basic Minimum Work Requirements : Minimum 2 years' experience in a High Complexity Clinical Laboratory is preferred. Must possess proficiency with basic computer programs. Be a strong team player. Excellent communication skills. Must be able to multitask and keep up in a fast-paced environment. Must work well on your own with minimal supervision. Basic Minimum Education Qualifications : Minimum of an Associate's or Bachelors of Science in Medical Technology, Clinical Laboratory Sciences, or a Life Science such as Biology or Chemistry Laboratory certification preferred Qualify as Testing Personnel as defined by CLIA rule § 493.1489 Position is full-time working Tuesday - Saturday, 8:00am - 5:00pm, schedule varies , additional hours as needed . Candidates currently living within a commutable distance of Huntsville, AL are encouraged to apply. Excellent full-time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.

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