Eurofins
The Molecular Technologist III is responsible for specimen labeling, processing, test performance, 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 TEM-PCR such as qPCR. Responsible for reviewing patient testing data and QC results and reporting test results when assigned.
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: Sample Correction, Stool Extraction, Array Plate Building and Proplate Pressing.
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.
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.
Enter, review, verify and release patient results in the Laboratory Information System.
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 effected 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.
Qualifications Basic Minimum Education Qualifications
Minimum of an Associate’s or Bachelor’s of Science in Medical Technology, Clinical Laboratory Sciences or a Life Science such as Biology or Chemistry.
Basic Minimum Qualifications
Minimum 2 years experience in a High Complexity Clinical Laboratory is preferred.
Laboratory certification preferred.
Qualify as Testing Personnel as defined by CLIA rule 493.1489.
Authorization to work in the United States indefinitely without restriction or sponsorship.
The Ideal Candidate Possesses the Following
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.
Additional Information Position is full‑time working Monday - Saturday (days varies) 7:00 am - 5:00 pm with overtime as needed. Candidates currently living within a commutable distance of Huntsville AL are encouraged to apply.
Benefits
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.
Remote Work: No
Employment Type: Full‑time
Key Skills
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Maintenance
Contract Management
Import & Export
Android Development
Experience: years
Vacancy: 1
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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: Sample Correction, Stool Extraction, Array Plate Building and Proplate Pressing.
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.
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.
Enter, review, verify and release patient results in the Laboratory Information System.
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 effected 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.
Qualifications Basic Minimum Education Qualifications
Minimum of an Associate’s or Bachelor’s of Science in Medical Technology, Clinical Laboratory Sciences or a Life Science such as Biology or Chemistry.
Basic Minimum Qualifications
Minimum 2 years experience in a High Complexity Clinical Laboratory is preferred.
Laboratory certification preferred.
Qualify as Testing Personnel as defined by CLIA rule 493.1489.
Authorization to work in the United States indefinitely without restriction or sponsorship.
The Ideal Candidate Possesses the Following
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.
Additional Information Position is full‑time working Monday - Saturday (days varies) 7:00 am - 5:00 pm with overtime as needed. Candidates currently living within a commutable distance of Huntsville AL are encouraged to apply.
Benefits
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.
Remote Work: No
Employment Type: Full‑time
Key Skills
Advertisement
Fireworks
Maintenance
Contract Management
Import & Export
Android Development
Experience: years
Vacancy: 1
#J-18808-Ljbffr