FISH Technologist III

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 fullservice 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 bestinclass 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 FISH Technologist III is responsible for performing all aspects of testing in a clinical FISH Laboratory. They evaluate and introduce new material methods and equipment to help determine the feasibility and/or adaptability for clinical FISH studies. They assist supervisors in the development of new technologies and participate in documenting and implementing Quality Assurance (QA)/ Quality Control (QC)/Quality Inventory (QI) procedures. Performs scanning and microscope analysis of chromosomes and interphase nuclei for FISH on a variety of cytogenetic specimens. Conducts imaging karyotyping tissue culture harvesting slide preparation and banding of specimens in suspensions and/or formalinfixed paraffinembedded tissues.

Key Job Elements

• Follows the laboratory procedures for specimen handling and processing test analyses reporting and maintaining records of patient test results.
• Performs and documents proficiency testing (PT) samples are tested in the same manner as patient specimens.
• Adheres to the laboratorys quality control policies documents all quality control activities instrument and procedural calibrations and maintenance performed.
• Follows the laboratorys established policies and procedures whenever test systems are not within the laboratorys established acceptable level of performance.
• Demonstrates capability of identifying problems that may adversely affect test performance or reporting of test results and must either correct the problems or immediately notify the General Supervisor technical Supervisor or Laboratory Director.
• Documents all corrective actions taken when test systems deviate from the laboratorys established performance specifications.
• Reports all concerns of test quality and/or patient safety to a Supervisor or Safety Officer.
• Demonstrates ability to perform all tasks required by a Technologist I and II.
• Consistently and independently performs the most complex levels of clinical laboratory testing.
• Determines the need for further studies to complete a diagnosis with the appropriate authority.
• Demonstrates the ability to detect and correct technical and operational problems. Assists in review of data for quality assurance.
• Exhibits skill and proficiency in applying technical principles and/or techniques of FISH. Conducts onthejob training for subordinate levels.
• Performs routine procedures including recording sample and patient information.
• Establishes and maintains sample cultures. Sets up cultures and harvests peripheral blood bone core lymph nodes and bone marrow samples.
• Demonstrates sterile techniques and basic measuring and uses laboratory equipment without assistance. Initiates troubleshooting steps to evaluate testing failures and other technical problems.
• Harvests cultures prepares and bands slides or applies FISH probes and slide processing.
• Assesses chromosome/slide quality and selects conditions for improvement to ensure maximum quality.
• Scans slides counts chromosomes and karyotype cells at the microscopic level on peripheral blood bone core lymph nodes and bone marrow samples.
• Accurate microscope analysis of cells and ISCN designations.
• Captures images on a computerized system and prepares karyotypes for final reports.
• Prepares final chromosome analysis and reports from culture initiation to final analysis of karyotypes. Utilizes imaging equipment for final review of cases.
• Accurately enter case results into the reporting system for review by the Director.
• Performs and documents preventative maintenance of lab equipment.

Knowledge/Experience

• Requires a Bachelor of Science in biology or a related field.
• 5 years of experience in high complexity testing in a cytogenetics clinical lab.
• Current ASCP certification CG(ASCP) required.
• Requires a high degree of care and attention with strict adherence to defined clinical testing protocols.
• Demonstrated skills in technical data interpretation and ability to troubleshoot.
• Proficient in Microsoft Office Suite specifically Word Excel Outlook and general working knowledge of the Internet for business use.
• Ability to work in a fastpaced deadlinedriven environment.
• Visual acuity (including color discrimination) and analytical skills to distinguish fine detail.
• Manual dexterity to use common laboratory equipment and perform sterile techniques as required.
• Must possess the ability to sit and/or stand for long periods of time.
• Must possess the ability to perform repetitive motion.
• Ability to lift up to 30 pounds.
• May be required to handle bloodborne pathogens and general laboratory reagents.
• Exposure to bodily fluids and some exposure to laboratory reagents including ethanol acetic acid and some xylene.

Lab Specific Qualifications

• Visual acuity (including color discrimination) and analytical skills to distinguish fine detail.
• Ability to tolerate extensive periods seated and/or standing.
• Must possess the ability to perform repetitive motion.
• Ability to lift up to 30 pounds.
• May have exposure to extreme temperatures high noise levels fumes and biohazardous material/chemicals including formalin in the lab environment.
• May be required to handle bloodborne pathogens and general laboratory reagents; handle live human specimens tissues and bodily fluids.

Environment

Fulgent Therapeutics LLC is an Equal Employment Opportunity Employer.

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. The term qualified individual with a disability means an individual with a disability who with or without reasonable accommodation can perform the essential functions of the position.

This job description reflects managements assignment of essential functions. Nothing in this job description restricts managements right to assign or reassign duties and responsibilities to this job at any time.

Please note that Fulgent (and its affiliated companies including Inform Diagnostics and CSI Laboratories) does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Search firms or agencies without an applicable contract and/or express approval to recruit for the role in question that choose to submit a resume or client information to our career page or to any employee of Fulgent will not be eligible for payment of any fee(s) and any associated shared data will become the property of Fulgent.