Fulgent Genetics jobs in Alpharetta, GA

Job Details Entry CSI Site - Alpharetta, GA Full Time High School BiotechDescription About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Under direct supervision, assists in the shipping of client results and materials back to the client, and accurately notes shipping details in the corresponding case. Returns will be thought FedEx, UPS and in-house courier. Consistently adheres to laboratory policies for safety, conduct and performances. Key Job Elements Ensures paraffin block(s) and stained slides are returned to the client in a timely fashion, based on case type. Enters shipments in the Fed Ex manager and prints Air Bill labels for shipping pouches. Accurately notes shipping details in the case and then completes the case in the LIS, when applicable. Reconciles empty boxes and disposes of damaged boxes. Ensures returned ice packs are placed in the freezer for reuse. Monitors, responds, and completes “Shipping Help” requests. Maintains clean work areas. Provides related responsibilities as required. Qualifications Knowledge/Experience HS Diploma, vocational education or higher, some college preferred. Additional Skills Ability to manage multiple projects at one time. High attention to detail. Laboratory/medical knowledge a plus. 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. Physical Requirements: A moderate amount of standing and sitting. Safety: Exposure to biological hazards associated with human specimens. Standard universal precautions required for handling specimens. 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.

Job Details Experienced CSI Site - Alpharetta, GA Full Time 4 Year Degree BiotechDescription About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Supervise the workflow of technical employees in the areas of routine cytogenetic analysis. May act as back-up for the lab manager. Provide guidance and technical assistance to other staff as necessary. Assist in the review of test results. Assist in the preparation of cases for reporting by reviewing karyotypes and accompanying documents to ensure cases are complete and free of errors prior to the reporting of results by the laboratory director. Key Job Elements Supervision: Supervise the daily workflow of chromosome analysis. Provide guidance and technical assistance to other staff as necessary Management: May serve as a back-up to the laboratory manager. May assist with managerial duties as needed in the absence of the laboratory manager Case Review: Assist in the pre-review of cases for correct clinical indication and patient information Workflow: Coordinate workflow on a daily basis to insure timely analysis and reporting of patient samples Reports: Review cases for accuracy of karyotypes, patient demographics, analysis information, nomenclature, and enters patients results prior to the final review by the laboratory director Recruiting: Participate in recruiting and interviewing of new applicants. Technical Manuals: Assist in updating and maintaining the laboratory standard operating procedures (SOP Manual) Personnel: Assist with annual employee competency documentations and employee evaluations Training: Coordinate training programs for new employees Technical Duties: Perform routine and moderate to complex tests and analysis as needed according to established procedures in designated technical area Resource: Acts as a technical resource for less experienced personnel regarding laboratory procedures and scope analysis Professional Development: Attends in-services, reads professional literature, and participates in educational programs and activities to remain abreast of developments in the field of cytogenetics Company Policies: Conforms to all company policies, maintains a professional attitude at all times Protocol Development: Assist in the development of the new protocols in clinical programs. Identifies ways in which laboratory procedures and activities can be modified to improve upon current methodologies Communication: Assures positive and timely communication with all staff and management staff; responsible for maintaining proper lines of communication Safety: Maintains a safe working environment by maintaining strict adherence to company safety policies and procedures; is aware of safety hazards and reports any unsafe conditions to the safety officer Compliance: Assures that the laboratory adheres to the compliance of policies set forth by the company and both governmental and non-governmental regulating agencies Qualifications Knowledge/Experience Bachelor's degree in biology or related scientific field. Six years of experience in cytogenetics laboratory. Certified as a Cytogenetic Technologist by the ASCP. Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency. Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually. Skills Possess good communication skills in order to accomplish tasks and instill teamwork within the laboratory. Possess working knowledge of laboratory procedures and instrumentation. Possess problem solving skills to evaluate, differentiate and resolve technical and instrumentation issues. 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. 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.

About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Responsible for the technical and operational oversight of the Genetics department. This includes the identification and implementation of process improvements, staff development, and performance management in relation to company and departmental goals. Coordinates research and development efforts to maximize and enhance test offerings and performance. Key Job Elements Oversee the operation of the Genetics department to maintain an efficient and quality lab. Ensure productivity, turnaround time, sample quality, failure rate, and abnormal rate meet departmental expectations; prepare monthly statistics reports including all of the above monitors; and make recommendations for necessary actions. Participate in the evaluation and validation of new procedures and instrumentation. Monitor the quality control assurance programs for the Genetics Department. Monthly quality controls are presented on a monthly basis, or immediately when obvious deviations from acceptable standards occur. Create, update, and maintain the laboratory standard operating procedures (SOP manual). Communicate and review all laboratory policies/procedures with the Laboratory Director for approval and implementation. Monitor staffing needs as volume increases and participate in the recruiting and interviewing of new applicants. Prepare semi-annual/annual evaluation of laboratory staff, make recommendations for salary increases, promotions, coaching, and performance improvement. Ensure a safe working environment by maintaining strict adherence to company safety policies and procedures. Assures that the laboratory adheres to compliance with policies set forth by the company and governmental and non-governmental regulating agencies. Participate in proficiency testing for the Genetics Department, including CAP/CLIA/OSHA Monitor quality improvement/established thresholds and make recommendations for corrective action and preventative action; prepare quality improvement reports and submit to laboratory director and quality manager for approval. Participates in the budgeting and planning process for the laboratory and reviews operational costs for proper cost containment. Participates in company meetings and conducts departmental meetings when applicable. Attends in-services, reads professional literature, and participates in educational programs and activities to remain abreast of developments in the fields of cytogenetics and FISH. Coordinates training programs with the training coordinator for new employees. Perform related tasks as assigned. Knowledge/Experience * Bachelor of Science in a laboratory science. * NCA/ASCP Certification. * Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency. * Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually. * 10 years genetics experience in a reference laboratory Genetics department. Including 3-5 years supervisory experience. Skills * Possess good communication skills in order to accomplish tasks and instill teamwork within the laboratory. * Possess working knowledge of laboratory procedures and instrumentation. * Possess problem solving skills to evaluate, differentiate and resolve technical and instrumentation issues. 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. 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.

Job Details Experienced CSI Site - Alpharetta, GA Full Time 4 Year Degree BiotechDescription About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Under direct supervision, leads staff in the triaging of specimens, handling of specimens, including storage and disposal of specimens, reagent preparation, and the storing of flow slides. Key Job Elements For Specimen Check In: Verifies that all specimens are properly labeled with appropriate patient identifiers, accurately records sample volumes in the Specimen Management module. For Specimen Check Out: Specimen is marked as checked out in the Specimen Management module. The specimen is labeled with additional case stickers, if necessary, then the specimen, travel doc, and/or requisition are given to the appropriate lab to begin testing. For Performing CBCs: Accurately prepares dilutions, correctly performs CBCs on the Sysmex, accurately records the count and the Sysmex machine number where the count was performed on the travel doc. Records the count in the Specimen Management module. Sample Splits: Observe principles of sterile technique in carrying out daily responsibilities for splitting samples and sample preparation for other departments. Correctly makes smears when the lab requests them. Send outs: Coordinates and prepares patient samples/pellets for shipment. Monitors outstanding sample requests to ensure they get to Accessioning to be sent out. Discards retained specimens/slides according to departmental protocols and timeframes. Monitors emails and tickets for specimen requests for add-ons and send-outs; monitors the response times to ensure the response is in a timely manner. Monitors the board in the Specimen Management area. Assists with pre-accessioning/pushing of incoming specimens when applicable. Completes cross-training in the process of accessioning all specimen types (data entry). Provides guidance and assists in prioritizing and batching specimens for processing, data entry, splitting samples, preparation for other departments, send out and disposal. Develops and updates SOPs, as needed, and oversees the implementation, evaluation and modification of such SOPs. Ensures the performance of all Specimen Management procedures according to the established SOPs. Organizes workflow and ensures that employees understand their duties and delegated tasks. Ensures adequate coverage in all areas of Specimen Management. Develops training materials and schedules for new employees and monitors progress. Performs initial and annual competency assessments once training is complete. Identifies and pursues opportunities for improvement in activities or processes according to internal quality procedures. Prepares Quality Indicator report components to demonstrate performance. Maintains clean work areas. Supplies: Assists in maintaining an adequate stock of commonly used supplies. Performs related responsibilities as required. Safety: Practice universal precaution measures necessary for the handling of patient samples and proper use of PPE when working in the laboratory. A moderate amount of standing is often required. Potential Exposure to toxic chemicals and the biohazards associated with handling blood, solid tissue, and body fluids. Possess manual dexterity in order to perform analytical testing. Qualifications Knowledge/Experience Bachelor's Degree in biological sciences or other related field. Laboratory/medical knowledge preferred but not required. Non-technical laboratory personnel must complete at least six hours of continuing education annually. Must possess human relations and communication skills in order to accomplish tasks. Ability to perform assigned tasks exactly according to prescribed procedures. High attention to detail. Ability to work in a fast-paced environment. Environment Fulgent Therapeutics LLC/CSI 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. 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.

Job Details Experienced CSI Site - Alpharetta, GA Full Time 2 Year Degree BiotechDescription About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Under minimal supervision, coordinates, oversees, and performs routine and specialized activities related to the operation of the Histology/IHC laboratory. Develops protocols, coordinates workflow and oversees quality control in specialized areas of the laboratory. Responsible for various techniques involved with preparation, processing and staining of tissue specimens for examination and diagnosis. Prepares microscopic slides for diagnostic purposes; performs diagnostic tests; maintains laboratory, equipment and records. Key Job Elements Prepares microscopic slides for patient diagnosis to include tissue processing, embedding and tissue orientation, sectioning of tissue blocks with preparation of microscopic slides, staining and submission of slides to Pathologist for diagnosis and reporting. Performs procedures within the scope of practice for a Histotechnician to include special staining procedures, immunohistochemistry and various other special procedures. Performs Molecular Pinpoint procedures. Quality Review of stained immunohistochemistry cases before released to clients and medical staff. Knowledgeable of correct CPT codes to enter when technical summaries are needed. Performs Bone marrow grossing. May also perform the grossing of more complex tissues specimens as trained under the supervision of CSI medical staff. Strives to meet established parameters such as departmental turnaround time (TAT). Utilizes the Laboratory Information System for processing and tracking, printing slide labels, ordering stains, and a variety of QA and reporting functions. Participates in the on-call program as needed and call back for off-shifts, weekends and holidays. Monitors inventory of the department and routinely restocks supplies and alerts leadership of the need for reordering. Maintains laboratory records and documentation as required by laboratory procedures and/or hospital record retention policies. Follows the chemical and recycling program for xylene and formalin. Follows established safety and biohazard procedures and standard precautions at all times. Disposes biohazardous wastes following laboratory protocols (see laboratory safety manual and chemical hygiene plan. Quality Assurance: Ensure compliance with quality control policies and procedures to ensure that all aspects of laboratory operation are performed in accordance with accepted standards and applicable laws for clinical laboratories. Participates in the development and/or maintenance of SOPs as required. Identifies ways in which laboratory procedures and activities can be modified to improve upon current methodologies. Leadership: Assists with assigned additional duties in a specialized area of the laboratory. Weekly workload log. Cut logs. Safety officer. Help maintain Preventative maintenance logs. Take weekly inventory. Help in the training of new staff members. Resource: Acts as a technical resource for less experienced personnel regarding laboratory procedures. Troubleshoot equipment issues. Helps in identifying and resolving stain quality issues. Performs other duties as assigned. Qualifications Knowledge/Experience AA Degree OR Equivalent combination of Education/Experience required. Bachelor's degree in Biological /Physical sciences preferred. HT (ASCP) Histotechnician certification required; HTL (ASCP) Histotechnologist preferred. Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency. Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually. A minimum of six (6) years of general histology lab experience, with immunohistochemistry experience preferred. Must satisfy CLIA regulations to perform high complexity testing. Working Conditions: The laboratory environment has an inherent risk of exposure to blood-borne pathogens, other pathogens such as TB, and the hazards associated with the chemical's formaldehyde and xylene. All safety policies and procedures must be observed to minimize these hazards. A moderate amount of standing is often required. The ability to lift approximately 25lbs is required. 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. 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.

About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Responsible for review and sign out of cytogenetic and fluorescent in-situ hybridization (FISH) cases. Key Job Elements Responsible for review and sign out of cytogenetic and FISH cases Application of accepted criteria in formulating and reporting diagnostic/prognostic information on various specimens including hematologic and solid tumor specimens. Ensure that the reports of test results include pertinent information required for interpretation. Collaboration with hematopathologists and surgical pathologists to provide appropriate diagnostic and prognostic interpretation. Interpretation/sign-out of pathology specimens within CAP guidelines for turnaround time. Provide clinical laboratory consultation to technical personnel and healthcare providers. Participation in Quality Assurance measures for the laboratory as required by accreditation standards. Provide residents and/or trainees information on specimen evaluation and reporting as needed. Provide on-call services as designated in department schedule Support with guidance and training of the Genetics analysis technologists, as needed Perform other responsibilities as requested or required by CLIA and other local, state, or federal regulations. Knowledge/Experience * Doctorate degree (PhD and/or MD) in genetics, molecular genetics, human genetics, or related field. * ABMGG board-certified or board-eligible in Clinical Cytogenetics, Genetics, or Laboratory Genetics and Genomics. * 0 - 5 years of relevant director-level experience in clinical cytogenetics; candidates who have recently completed a relevant fellowship and are board-eligible will be considered for this position. * Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency. * Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually. 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. 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.

Job Details Entry CSI Site - Alpharetta, GA Full Time High School Customer ServiceDescription About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Responsible for specialized customer service duties necessary to maintain an efficient and high-quality lab operation. Serves as initial point of contact with all clients, CSI Account Managers and other callers. Key Job Elements Provide prompt, courteous, and professional customer service to all internal and external clients of CSI Laboratories. Triage calls, handle questions and direct callers to appropriate personnel/department. Resolve all client and internal case concerns via email and ticket in a timely manner. Learn to navigate laboratory information systems to identify cases and distribute final diagnostic reports to appropriate clients. Fulfill client requests for specimen kits and materials, RPMI and other needed supplies. Schedule specimen pick-ups. Maintain accurate and up-to-date logs, worksheets and comments to database to assure immediate access to information. Provide support to Company's Medical Directors in obtaining additional clinical history from clients, tracking cases and final reports. Accurately add/cancel tests; provide specimen requirements. Operate office equipment including computers, scanners, copiers, etc. Be available for on-call duty to handle urgent calls from clients and CSI account managers Qualifications Knowledge/Experience 1-3 years of proven customer service and/or administrative experience in a fast-paced environment (prefer experience in healthcare/laboratory setting). Experience handling multiple projects at one time. Ability to communicate effectively - both written and oral. Motivated to work independently and within a team environment. Proficient with Microsoft Office programs. Ability to handle stressful situations High School Diploma. Some college preferred. Non-technical laboratory personnel must complete at least six hours of continuing education annually. 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. 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.

About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Supervise the workflow of the Histology/IHC Laboratory; train all new technologists in laboratory methods and procedures; provide guidance and technical assistance to other staff as necessary. Assist in the review of test results; review and write SOP's; assist in the development of clinical performance improvement measures. Key Job Elements Perform quality control and quality assurance on instrumentation and reagents used for patient testing. Perform validation studies for new instrumentation, reagents, and protocols. Oversee and direct the daily operation of the IHC laboratory. Participate in the evaluation and validation of new procedures and instrumentation. Assist the IHC Manager with monthly QM/QA projects. Work closely with the pathologists to develop and maintain quality and efficient staining protocols. Perform related tasks as assigned. Knowledge/Experience * BS in Biological/Physical Science preferred. * HT (ASCP) or HTL (ASCP) certification required. * Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency. * Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually. * QIHC Specialty preferred. * Minimum of 6 years of laboratory experience. * Must satisfy CLIA regulations to perform high complexity testing. 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 accommodation 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. Working Conditions * The laboratory environment has an inherent risk of exposure to blood-borne pathogens, other pathogens such as TB, and the hazards associated with the chemicals formaldehyde and xylene. All safety policies and procedures must be observed to minimize these hazards. * Moderate amount of standing is often required. * Ability to lift approximately 25lbs is required. 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.

About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Responsible for review and sign out of cytogenetic and fluorescent in-situ hybridization (FISH) cases. Key Job Elements Responsible for review and sign out of cytogenetic and FISH cases Application of accepted criteria in formulating and reporting diagnostic/prognostic information on various specimens including hematologic and solid tumor specimens. Ensure that the reports of test results include pertinent information required for interpretation. Collaboration with hematopathologists and surgical pathologists to provide appropriate diagnostic and prognostic interpretation. Interpretation/sign-out of pathology specimens within CAP guidelines for turnaround time. Provide clinical laboratory consultation to technical personnel and healthcare providers. Participation in Quality Assurance measures for the laboratory as required by accreditation standards. Provide residents and/or trainees information on specimen evaluation and reporting as needed. Provide on-call services as designated in department schedule Support with guidance and training of the Genetics analysis technologists, as needed Perform other responsibilities as requested or required by CLIA and other local, state, or federal regulations. Knowledge/Experience * Doctorate degree (PhD and/or MD) in genetics, molecular genetics, human genetics, or related field. * ABMGG board-certified in Clinical Cytogenetics, Genetics, or Laboratory Genetics and Genomics. * 5+ years of relevant director-level experience in clinical cytogenetics. * Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency. * Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually. 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. 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.

About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Under direct supervision, performs laboratory procedures at an entry-level capacity in accordance with standard procedures. Rotate through each section of the laboratory and develops proficiency in cell culture and harvest, microscope monitor analysis of chromosomes for detection of abnormalities, and the preparation of karyotypes. Adheres to laboratory policies for safety, conduct, and performance. *This is an 18-month position. Upon passing the certification exam, the trainee will be eligible for a promotion to Genetic Technologist I. Key Job Elements Cell Culture: Handle, prepare, and process various specimens; learn to identify appropriate specimens for study, and methods of collection, preservation, and transport; learn the appropriate culture techniques for a variety of specimen types; understand the principles and techniques for harvesting cell cultures of human tissue for genetic testing; apply knowledge of cell cycle for various cell types and culture conditions; understand the principles and techniques of chromosome banding and staining; develop troubleshooting skills to obtain optimal banding and staining results. Charts/Records: Learn to maintain necessary records and laboratory database in logbooks and computers as related to specimens. Records pertinent laboratory data on the appropriate form or chart to ensure accurate and complete documentation of laboratory findings. Microscopy/Analysis: Learn to properly align all optical components of the microscope to guarantee that the lamp is centered, and the condenser and field diaphragm are properly adjusted for Kohler Illumination. Learn to select suitable metaphases for analysis and become proficient in the detection of numerical and structural abnormalities. Learn to accurately record complete documentation of analytical findings. Learn how to use GSL scanning system. Imaging: Learn to use specialized equipment for capture and enhancement of images at optimum resolution. Professional Development: Attends in-services, reads professional literature, and participates in educational programs and activities to remain abreast of developments in the field of cytogenetics. Quality Control: Complies with quality control policies and procedures to ensure that all aspects of laboratory operation are performed in accordance with accepted standards and applicable laws for clinical laboratories. Reagents/Media: Establish good laboratory practice skills; learn to operate, clean and maintain all laboratory equipment and instruments needed to prepare reagents, stains, and media in accordance with laboratory protocol. Staining: Learn to perform staining procedures for routine and specialized analysis. Safety: Understand and perform universal precaution measures necessary for the handling of fresh body fluids. Sterile Technique: Observes principles of sterile technique in carrying out daily responsibilities including the proper cleaning and sterilization of work surfaces. Supplies: Assist in maintaining an adequate stock of commonly used supplies. Performs related responsibilities as required. Knowledge/Experience * Bachelor's degree in biology or related scientific field. * Experience in laboratory sciences desired but not required. * Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency. * Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually. Environment Fulgent Therapeutics LLC/CSI 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. * Potential Exposure to toxic chemicals and the bio-hazards associated with handling blood, solid tissue, and body fluids. 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.

About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Courier will ensure samples are delivered and/or picked up from doctor's offices, laboratories and hospitals as necessary. Courier follows a designated route containing daily and will call locations. Courier is responsible for providing excellent customer service and maintaining a professional demeanor with clients. Follow all applicable laws and safety regulations. Proof of current auto insurance coverage as required by CSI. Ability to drive to multiple locations totaling 350 miles daily. Key Job Elements Ensure samples are delivered and/or picked up, as necessary. Be at the specified pick-up and/or drop off locations at the times specified, within reason. Ensure that all samples are safely and securely stored in the courier vehicle. Maintain accurate records, including vehicle logs, pick-up/drop off logs and client communications. Report any accidents, delays, or any other traffic and transportation situations for required follow-up by Supervisor. Respond to all calls or voicemails in regards to pick-ups, missed pick-ups or additional instructions. Maintain an accident and citation free record. Other duties may be assigned by Supervisor as needed. Knowledge/Experience * High School Diploma or equivalent * Excellent communication skills * Ability to work unsupervised with an emphasis on punctuality * Ability to lift 25 lbs. * Ability to sit in a car for long periods of time (minimum 2 hours) * Non-technical laboratory personnel must complete at least six hours of continuing education annually. 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. 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.

Job Details Entry CSI Site - Alpharetta, GA Part Time High School BiotechDescription About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Under direct supervision, assists in the verification, ordering and triage of specimens, scans documents into the LIS system, faxes add/cancel requests to clients, ships client's results, and assists with sending out referral lab test requests. Consistently adheres to laboratory policies for safety, conduct, and performances. Key Job Elements Accurately accession all specimen/test types and verifies all specimens are properly identified. Processes work completely and accurately, to include requisitions and any additional documents accompanying specimens, within departmental guidelines and time frame. Easily and accurately navigates through the LIS, emails, and tickets. Accurately scans accessioning documents, requisitions, and pertinent attachments into content central, performing initial QC and creating folders, when necessary. Performs accessioning QC accurately and within the established time frame, prioritizing the Flow cases. Ensures that blocks and/or stained slides are accurately packed up for return to the clients by CSI courier or Fed Ex in a timely manner. Demonstrates punctuality and adheres to the set work schedule. Accurately orders and documents any test that must be sent out to a referral laboratory. This includes properly completing the appropriate test requisitions, labeling and logging the specimens, packing for shipping to the referral lab, and adding appropriate case notes. Accurately adds testing from the Add-On queue, assigning the correct case status button. Adds thorough case notes for the added testing. Faxes add/cancel forms to clients and monitors to ensure transmittal. Routinely monitors the fax machine for incoming faxes and distributes to the appropriate designee. Maintains complete, accurate and up-to-date documents such as equipment logs and worksheets, such that information can be accessed in a timely manner. Maintains clean work areas. Performs related responsibilities as required. Qualifications Knowledge/Experience HS Diploma, vocational education or higher Bachelor's degree in biological science is preferred. Non-technical laboratory personnel must complete at least six hours of continuing education annually. Ability to manage multiple projects at one time. Excellent verbal and written communication skills. High attention to detail. Laboratory/medical knowledge a plus. Environment Fulgent Therapeutics LLC/CSI 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. Physical Requirements: A moderate amount of standing and sitting. Safety: Exposure to biological hazards associated with human specimens. Standard universal precautions required for handling specimens. 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.

Job Details Entry CSI Site - Alpharetta, GA Full Time High School Admin - ClericalDescription About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Responsible for providing administrative and clerical services in order ensure effective and efficient administrative operations. Support of billing and administrative operations. Key Job Elements Requesting missing billing/patient information from the clients via email, fax, and/or phone. Demographic Entry/Updated Order Entry into Quadax. Insurance Verification. Uploading of documents received to corresponding systems. Processing physical mail correspondences and mailing to the lockbox. Managing and Filing patient records in the storage. Performs related responsibilities as required and/or directed by management. Qualifications Knowledge/Experience HS Diploma 1-year related office experience including familiarity with Microsoft Office products. Non-technical laboratory personnel must complete at least six hours of continuing education annually. 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. 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.

Job Details Management CSI Site - Alpharetta, GA Full Time 4 Year Degree BiotechDescription About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Responsible for the technical and operational oversight of the Genetics department. This includes the identification and implementation of process improvements, staff development, and performance management in relation to company and departmental goals. Coordinates research and development efforts to maximize and enhance test offerings and performance. Key Job Elements Oversee the operation of the Genetics department to maintain an efficient and quality lab. Ensure productivity, turnaround time, sample quality, failure rate, and abnormal rate meet departmental expectations; prepare monthly statistics reports including all of the above monitors; and make recommendations for necessary actions. Participate in the evaluation and validation of new procedures and instrumentation. Monitor the quality control assurance programs for the Genetics Department. Monthly quality controls are presented on a monthly basis, or immediately when obvious deviations from acceptable standards occur. Create, update, and maintain the laboratory standard operating procedures (SOP manual). Communicate and review all laboratory policies/procedures with the Laboratory Director for approval and implementation. Monitor staffing needs as volume increases and participate in the recruiting and interviewing of new applicants. Prepare semi-annual/annual evaluation of laboratory staff, make recommendations for salary increases, promotions, coaching, and performance improvement. Ensure a safe working environment by maintaining strict adherence to company safety policies and procedures. Assures that the laboratory adheres to compliance with policies set forth by the company and governmental and non-governmental regulating agencies. Participate in proficiency testing for the Genetics Department, including CAP/CLIA/OSHA Monitor quality improvement/established thresholds and make recommendations for corrective action and preventative action; prepare quality improvement reports and submit to laboratory director and quality manager for approval. Participates in the budgeting and planning process for the laboratory and reviews operational costs for proper cost containment. Participates in company meetings and conducts departmental meetings when applicable. Attends in-services, reads professional literature, and participates in educational programs and activities to remain abreast of developments in the fields of cytogenetics and FISH. Coordinates training programs with the training coordinator for new employees. Perform related tasks as assigned. Qualifications Knowledge/Experience Bachelor of Science in a laboratory science. NCA/ASCP Certification. Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency. Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually. 10 years genetics experience in a reference laboratory Genetics department. Including 3-5 years supervisory experience. Skills Possess good communication skills in order to accomplish tasks and instill teamwork within the laboratory. Possess working knowledge of laboratory procedures and instrumentation. Possess problem solving skills to evaluate, differentiate and resolve technical and instrumentation issues. 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. 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.

About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Responsible for various duties within the HIS/IHC laboratory, including delivery of completed cases to the medical team, assisting technical personnel with slide preparation which includes labeling slides for sectioning and removing/organizing completed slides after staining. Other duties may include assistance with the routine maintenance of various equipment utilized in the laboratory. Key Job Elements Assist with the organization and delivery of new and/or completed cases to the medical team or Accessioning for return to the client. Prepares cases for sectioning by comparing specimen identifying numbers with all associated paperwork, pulling appropriate controls, and labeling slides with correct identifying criteria. Provide assistance to the technician operating the immunostainers by assisting with QC of slides and/or lables, removing the stained slides from the instrument in preparation for quality control review. Assist with the routine maintenance on the instrumentation utilized in the histology/IHC laboratory. This includes such tasks as emptying the chemical waste for disposal, filling the bulk fluids for operation, and basic cleaning steps. Monitors inventory of the department and routinely restocks supplies and alerts leadership of the need for reordering. Maintains laboratory records and documentation as required by laboratory procedures and/or hospital record retention policies. Follows established safety and biohazard procedures and standard precautions at all times. Disposes biohazardous wastes following laboratory protocols (see laboratory safety manual and chemical hygiene plan. Quality Assurance: Ensure compliance with quality control policies and procedures to ensure that all aspects of laboratory operation are performed in accordance with accepted standards and applicable laws for clinical laboratories. Perform other duties as assigned. Knowledge/Experience * High School graduate or equivalent. Working Conditions The laboratory environment has an inherent risk of exposure to bloodborne pathogens, other pathogens such as TB, and the hazards associated with the chemicals formaldehyde and xylene. All safety policies and procedures must be observed to minimize these hazards. A moderate amount of standing is often required. The ability to lift approximately 25lbs is required. 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. 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.

Job Details Entry CSI Site - Alpharetta, GA Full Time 4 Year Degree BiotechDescription About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Under direct supervision, performs laboratory procedures at an entry-level capacity in accordance with standard procedures. Rotate through each section of the laboratory and develops proficiency in cell culture and harvest, microscope monitor analysis of chromosomes for detection of abnormalities, and the preparation of karyotypes. Adheres to laboratory policies for safety, conduct, and performance. *This is an 18-month position. Upon passing the certification exam, the trainee will be eligible for a promotion to Genetic Technologist I. Key Job Elements Cell Culture: Handle, prepare, and process various specimens; learn to identify appropriate specimens for study, and methods of collection, preservation, and transport; learn the appropriate culture techniques for a variety of specimen types; understand the principles and techniques for harvesting cell cultures of human tissue for genetic testing; apply knowledge of cell cycle for various cell types and culture conditions; understand the principles and techniques of chromosome banding and staining; develop troubleshooting skills to obtain optimal banding and staining results. Charts/Records: Learn to maintain necessary records and laboratory database in logbooks and computers as related to specimens. Records pertinent laboratory data on the appropriate form or chart to ensure accurate and complete documentation of laboratory findings. Microscopy/Analysis: Learn to properly align all optical components of the microscope to guarantee that the lamp is centered, and the condenser and field diaphragm are properly adjusted for Kohler Illumination. Learn to select suitable metaphases for analysis and become proficient in the detection of numerical and structural abnormalities. Learn to accurately record complete documentation of analytical findings. Learn how to use GSL scanning system. Imaging: Learn to use specialized equipment for capture and enhancement of images at optimum resolution. Professional Development: Attends in-services, reads professional literature, and participates in educational programs and activities to remain abreast of developments in the field of cytogenetics. Quality Control: Complies with quality control policies and procedures to ensure that all aspects of laboratory operation are performed in accordance with accepted standards and applicable laws for clinical laboratories. Reagents/Media: Establish good laboratory practice skills; learn to operate, clean and maintain all laboratory equipment and instruments needed to prepare reagents, stains, and media in accordance with laboratory protocol. Staining: Learn to perform staining procedures for routine and specialized analysis. Safety: Understand and perform universal precaution measures necessary for the handling of fresh body fluids. Sterile Technique: Observes principles of sterile technique in carrying out daily responsibilities including the proper cleaning and sterilization of work surfaces. Supplies: Assist in maintaining an adequate stock of commonly used supplies. Performs related responsibilities as required. Qualifications Knowledge/Experience Bachelor's degree in biology or related scientific field. Experience in laboratory sciences desired but not required. Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency. Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually. Environment Fulgent Therapeutics LLC/CSI 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. Potential Exposure to toxic chemicals and the bio-hazards associated with handling blood, solid tissue, and body fluids. 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.

About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Under minimal supervision, coordinates, oversees, and performs routine and specialized activities related to the operation of the Histology/IHC laboratory. Develops protocols, coordinates workflow and oversees quality control in specialized areas of the laboratory. Responsible for various techniques involved with preparation, processing and staining of tissue specimens for examination and diagnosis. Prepares microscopic slides for diagnostic purposes; performs diagnostic tests; maintains laboratory, equipment and records. Key Job Elements Prepares microscopic slides for patient diagnosis to include tissue processing, embedding and tissue orientation, sectioning of tissue blocks with preparation of microscopic slides, staining and submission of slides to Pathologist for diagnosis and reporting. Performs procedures within the scope of practice for a Histotechnician to include special staining procedures, immunohistochemistry and various other special procedures. Performs Molecular Pinpoint procedures. Quality Review of stained immunohistochemistry cases before released to clients and medical staff. Knowledgeable of correct CPT codes to enter when technical summaries are needed. Performs Bone marrow grossing. May also perform the grossing of more complex tissues specimens as trained under the supervision of CSI medical staff. Strives to meet established parameters such as departmental turnaround time (TAT). Utilizes the Laboratory Information System for processing and tracking, printing slide labels, ordering stains, and a variety of QA and reporting functions. Participates in the on-call program as needed and call back for off-shifts, weekends and holidays. Monitors inventory of the department and routinely restocks supplies and alerts leadership of the need for reordering. Maintains laboratory records and documentation as required by laboratory procedures and/or hospital record retention policies. Follows the chemical and recycling program for xylene and formalin. Follows established safety and biohazard procedures and standard precautions at all times. Disposes biohazardous wastes following laboratory protocols (see laboratory safety manual and chemical hygiene plan. Quality Assurance: Ensure compliance with quality control policies and procedures to ensure that all aspects of laboratory operation are performed in accordance with accepted standards and applicable laws for clinical laboratories. Participates in the development and/or maintenance of SOPs as required. Identifies ways in which laboratory procedures and activities can be modified to improve upon current methodologies. Leadership: Assists with assigned additional duties in a specialized area of the laboratory. Weekly workload log. Cut logs. Safety officer. Help maintain Preventative maintenance logs. Take weekly inventory. Help in the training of new staff members. Resource: Acts as a technical resource for less experienced personnel regarding laboratory procedures. Troubleshoot equipment issues. Helps in identifying and resolving stain quality issues. Performs other duties as assigned. Knowledge/Experience * AA Degree OR Equivalent combination of Education/Experience required. * Bachelor's degree in Biological /Physical sciences preferred. * HT (ASCP) Histotechnician certification required; HTL (ASCP) Histotechnologist preferred. * Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency. * Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually. * A minimum of six (6) years of general histology lab experience, with immunohistochemistry experience preferred. * Must satisfy CLIA regulations to perform high complexity testing. Working Conditions: * The laboratory environment has an inherent risk of exposure to blood-borne pathogens, other pathogens such as TB, and the hazards associated with the chemical's formaldehyde and xylene. All safety policies and procedures must be observed to minimize these hazards. * A moderate amount of standing is often required. * The ability to lift approximately 25lbs is required. 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. 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.

Job Details Entry CSI Site - Alpharetta, GA Full Time 4 Year Degree BiotechDescription About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Perform routine Flow Cytometry processing for Leukemia/Lymphoma and PNH testing. Assist Specimen Management in the triage and proper handling of specimens, including sterile split technique. Key Job Elements Sample Preparation: Identify, lyse, and stain samples for flow cytometric testing. Sample Sharing: Observe principles of sterile technique in carrying out daily responsibilities for splitting samples and sample preparation for other departments. Specimen Management: Accurately verify that all specimens are properly identified, process work completely and accurately, to include requisitions and any additional documents accompanying specimens. Reports: Locate and maintain patient reports/folders using laboratory LIS Professional Development: Attends in-services, reads professional literature, and participates in educational programs and activities to remain abreast of developments in the field of flow cytometry. Professional Training: Studies content to take and pass a certification exam in Immunology through American Association of Bioanalysts (Theory and Principles of Immunology, Immunology Practices and Laboratory Methods, Immune Disorders, Infectious Disease Immunology, Tumor Immunology and Transplantation Immunology, Quality Control, Quality Assurance, Quality Improvement, and Laboratory Compliance). Quality Control: Comply with quality control policies and procedures to ensure that all aspects of laboratory operation are performed in accordance with accepted standards and applicable laws for clinical laboratories. Reagents/Media: Prepare reagents, stains, and media in accordance with laboratory protocol. Safety: Practice universal precautions measures necessary for the handling of patient samples and proper use of PPE when working in the laboratory. Supplies: Assist in maintaining an adequate stock of commonly used supplies. Perform related responsibilities as required. Qualifications Knowledge/Experience Bachelor's degree in laboratory science or related scientific field and eligible for certification as a Medical Technologist; MT(AAB) Laboratory personnel participating in licensure or certification maintenance programs must complete the number of continuing education hours prescribed by their licensing or certifying agency. Technical laboratory personnel whose certification has been grandfathered and does not require participation in a certification maintenance program must complete at least twelve hours of continuing education annually. Laboratory experience preferred Environment Fulgent Therapeutics LLC/CSI 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. A moderate amount of standing is often required. Possess manual dexterity in order to perform analytical testing. Potential Exposure to toxic chemicals and the bio-hazards associated with handling blood, solid tissue, and body fluids. 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.

Job Details Entry CSI Site - Alpharetta, GA Full Time High School BiotechDescription About Us CSI Laboratories, a Fulgent Genetics Company, is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients. Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service 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 best-in-class 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 Under direct supervision, assists in the verification, ordering and triage of specimens, scans documents into the LIS, faxes add/cancel requests to clients, and assists with sending out reference lab test requests. Consistently adheres to laboratory policies for safety, conduct and performance. Key Job Elements Accurately accession all specimen/test types and verifies all specimens are properly identified. Processes work completely and accurately, to include requisitions and any additional documents accompanying specimens, within departmental guidelines and time frame. Easily and accurately navigates through the LIS, emails, and tickets. Accurately scans accessioning documents, requisitions, and pertinent attachments into content central, performing initial QC. Performs accessioning QC accurately and within the established time frame, prioritizing the Flow cases. Demonstrates punctuality and adheres to the set work schedule. Accurately orders and documents any test that must be sent out to a reference laboratory. This includes properly completing the appropriate test requisitions, labeling and logging the specimens, packing for shipping to the reference lab, and adding appropriate case notes. Accurately adds testing from the Add-On queue, assigning the correct case status button. Adds thorough case notes for the added testing. Faxes add/cancel forms to clients and monitors to ensure transmittal. Maintains complete, accurate and up-to-date documents such as equipment logs and worksheets, such that information can be accessed in a timely manner. Demonstrates thorough knowledge of all processes/procedures to the degree they can actively participate in the training of new employees. Provides guidance and assistance in prioritizing and batching and/or separating specimens for processing and data entry. Monitors the accessioning emails and tickets to verify responses. Actively participates in the training of new employees. Assists other departments with questions and issues. Monitors the supply inventory, including printer cartridge and toner inventory, and notifies supervisor when necessary. Shows initiative and takes on additional tasks without being asked. Qualifications Knowledge/Experience Up to 2 years laboratory experience HS Diploma, vocational education or higher - Bachelors Degree in biological science preferred Non-technical laboratory personnel must complete at least six hours of continuing education annually. Additional Skills Ability to manage multiple projects at one time. Excellent verbal and written communication skills. High attention to detail. Knowledge of laboratory/medical terminology. Physical Requirements: A moderate amount of standing and sitting. Safety: Exposure to biological hazards associated with human specimens. Standard universal precautions required for handling specimens. 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. 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.