City/State Norfolk, VA Work Shift First (Days) Overview: Sentara Norfolk General Hospital in Norfolk, VA is hiring a Molecular Diagnostic Scientist tech to work full-time day shifts () in Molecular Diagnostics. Sign on bonus up to $20,000 for qualified candidates! As a Molecular Technologist duties are to preform molecular microbiology and molecular pathology based laboratory tests; utilizes critical thinking skills to interpret complex test results; documents and reports test results; maintains equipment, instruments, and tools. Understands the molecular laboratory workflow and contamination risks. Communicates clearly with pathologists and physicians. Demonstrates fiscal responsibility with regard to reagent and consumable usage. Strong time management skills are necessary to effectively complete workload Education Bachelor's in medical technology or Biology/Chemical/Physical Science Certification/Licensure ASCP, AMT, or AAB certification Eligible for certification Must obtain Molecular certification in 1 year keyword: MLS, medical laboratory scientist, MT, CLS, Clinical lab Specialist, Talroo-Allied Health , Laboratory Services, Molecular Technologist, MB . Benefits: Caring For Your Family and Your Career • Medical, Dental, Vision plans • Adoption, Fertility and Surrogacy Reimbursement up to $10,000 • Paid Time Off and Sick Leave • Paid Parental & Family Caregiver Leave • Emergency Backup Care • Long-Term, Short-Term Disability, and Critical Illness plans • Life Insurance • 401k/403B with Employer Match • Tuition Assistance - $5,250/year and discounted educational opportunities through Guild Education • Student Debt Pay Down - $10,000 • Reimbursement for certifications and free access to complete CEUs and professional development • Pet Insurance • Legal Resources Plan • Colleagues may have the opportunity to earn an annual discretionary bonus if established system and employee eligibility criteria is met Here at Sentara, we are committed to consistently enhancing our training, advancement tracks, work-life benefits, and more. Our goal is to make you feel more excited to be here every day! Sentara Norfolk General Hospital , located in Norfolk, VA, is a 525-bed tertiary care facility that is home to the only Level I Adult Trauma Center and burn trauma unit in Hampton Roads, and also serves as the primary teaching hospital for Eastern Virginia Medical School. In addition to the high-quality heart program at Sentara Heart Hospital, our facility is home to Nightingale Regional Air Ambulance and several other dedicated facilities and specialized services. As a recognized accredited Comprehensive Stroke Center, and Magnet hospital for nursing excellence, our hospital specializes in heart and vascular, neurosciences, neurosurgery, urology, oncology, spine care, advanced imaging, behavioral health, maternity, and women's health, including a state-of-the-art neonatal intensive care unit. Sentara Health is an equal opportunity employer and prides itself on the diversity and inclusiveness of its close to an almost 30,000-member workforce. Diversity, inclusion, and belonging is a guiding principle of the organization to ensure its workforce reflects the communities it serves. In support of our mission "to improve health every day," this is a tobacco-free environment. For positions that are available as remote work, Sentara Health employs associates in the following states: Alabama, Delaware, Florida, Georgia, Idaho, Indiana, Kansas, Louisiana, Maine, Maryland, Minnesota, Nebraska, Nevada, New Hampshire, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, and Wyoming.
12/11/2025
Full time
City/State Norfolk, VA Work Shift First (Days) Overview: Sentara Norfolk General Hospital in Norfolk, VA is hiring a Molecular Diagnostic Scientist tech to work full-time day shifts () in Molecular Diagnostics. Sign on bonus up to $20,000 for qualified candidates! As a Molecular Technologist duties are to preform molecular microbiology and molecular pathology based laboratory tests; utilizes critical thinking skills to interpret complex test results; documents and reports test results; maintains equipment, instruments, and tools. Understands the molecular laboratory workflow and contamination risks. Communicates clearly with pathologists and physicians. Demonstrates fiscal responsibility with regard to reagent and consumable usage. Strong time management skills are necessary to effectively complete workload Education Bachelor's in medical technology or Biology/Chemical/Physical Science Certification/Licensure ASCP, AMT, or AAB certification Eligible for certification Must obtain Molecular certification in 1 year keyword: MLS, medical laboratory scientist, MT, CLS, Clinical lab Specialist, Talroo-Allied Health , Laboratory Services, Molecular Technologist, MB . Benefits: Caring For Your Family and Your Career • Medical, Dental, Vision plans • Adoption, Fertility and Surrogacy Reimbursement up to $10,000 • Paid Time Off and Sick Leave • Paid Parental & Family Caregiver Leave • Emergency Backup Care • Long-Term, Short-Term Disability, and Critical Illness plans • Life Insurance • 401k/403B with Employer Match • Tuition Assistance - $5,250/year and discounted educational opportunities through Guild Education • Student Debt Pay Down - $10,000 • Reimbursement for certifications and free access to complete CEUs and professional development • Pet Insurance • Legal Resources Plan • Colleagues may have the opportunity to earn an annual discretionary bonus if established system and employee eligibility criteria is met Here at Sentara, we are committed to consistently enhancing our training, advancement tracks, work-life benefits, and more. Our goal is to make you feel more excited to be here every day! Sentara Norfolk General Hospital , located in Norfolk, VA, is a 525-bed tertiary care facility that is home to the only Level I Adult Trauma Center and burn trauma unit in Hampton Roads, and also serves as the primary teaching hospital for Eastern Virginia Medical School. In addition to the high-quality heart program at Sentara Heart Hospital, our facility is home to Nightingale Regional Air Ambulance and several other dedicated facilities and specialized services. As a recognized accredited Comprehensive Stroke Center, and Magnet hospital for nursing excellence, our hospital specializes in heart and vascular, neurosciences, neurosurgery, urology, oncology, spine care, advanced imaging, behavioral health, maternity, and women's health, including a state-of-the-art neonatal intensive care unit. Sentara Health is an equal opportunity employer and prides itself on the diversity and inclusiveness of its close to an almost 30,000-member workforce. Diversity, inclusion, and belonging is a guiding principle of the organization to ensure its workforce reflects the communities it serves. In support of our mission "to improve health every day," this is a tobacco-free environment. For positions that are available as remote work, Sentara Health employs associates in the following states: Alabama, Delaware, Florida, Georgia, Idaho, Indiana, Kansas, Louisiana, Maine, Maryland, Minnesota, Nebraska, Nevada, New Hampshire, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, and Wyoming.
Cytotechnologist (Permanent Full Time Onsite Position) Join a fast-paced diagnostic laboratory that specializes in advanced molecular testing, including PCR-based diagnostics , with a focus on gynecology, infectious diseases, tick-borne illnesses, mycology, and chronic fatigue syndrome (CFS) . Currently seeking a Cytotechnologist to support high-quality specimen screening and evaluation. Position Summary: As a Cytotechnologist , you will play a critical role in identifying cellular abnormalities and assisting pathologists in making timely and accurate diagnoses. You'll perform both gynecological and non-gynecological microscopic evaluations , ensuring quality and precision throughout. Key Responsibilities: Perform microscopic screening of cellular samples using established cytological criteria Document specimen evaluations and ensure proper turnaround time Collaborate with supervisory cytotechnologists and pathologists for result correlation Maintain lab safety protocols and equipment Prepare high-quality cytology slides using approved laboratory methods Ensure patient confidentiality and data accuracy Contribute to team efforts with initiative and accountability Qualifications: Bachelor s degree in a related science field ASCP Board Certification required All levels of experience accepted (new grads encouraged to apply) Experience with ThinPrep Imaging System and Review Scope is a plus What We Offer: Competitive salary based on experience Full range of benefits: Medical, Dental & Vision Insurance Short & Long Term Disability, Life Insurance Flexible Spending Accounts & Voluntary Insurance Options Identity Theft Protection 401(k) Retirement Plan Paid Vacation & Holidays Business Casual Dress Code Interested?! Apply TODAY! You can also call/text me, Olivia Sloane, at and send an updated resume to with the best time and phone number for me to reach you as well! You can also schedule an appointment with my calendar: Olivia Sloane Client Relationship Manager & Senior Healthcare Recruiter, K.A. Recruiting, Inc.
12/10/2025
Full time
Cytotechnologist (Permanent Full Time Onsite Position) Join a fast-paced diagnostic laboratory that specializes in advanced molecular testing, including PCR-based diagnostics , with a focus on gynecology, infectious diseases, tick-borne illnesses, mycology, and chronic fatigue syndrome (CFS) . Currently seeking a Cytotechnologist to support high-quality specimen screening and evaluation. Position Summary: As a Cytotechnologist , you will play a critical role in identifying cellular abnormalities and assisting pathologists in making timely and accurate diagnoses. You'll perform both gynecological and non-gynecological microscopic evaluations , ensuring quality and precision throughout. Key Responsibilities: Perform microscopic screening of cellular samples using established cytological criteria Document specimen evaluations and ensure proper turnaround time Collaborate with supervisory cytotechnologists and pathologists for result correlation Maintain lab safety protocols and equipment Prepare high-quality cytology slides using approved laboratory methods Ensure patient confidentiality and data accuracy Contribute to team efforts with initiative and accountability Qualifications: Bachelor s degree in a related science field ASCP Board Certification required All levels of experience accepted (new grads encouraged to apply) Experience with ThinPrep Imaging System and Review Scope is a plus What We Offer: Competitive salary based on experience Full range of benefits: Medical, Dental & Vision Insurance Short & Long Term Disability, Life Insurance Flexible Spending Accounts & Voluntary Insurance Options Identity Theft Protection 401(k) Retirement Plan Paid Vacation & Holidays Business Casual Dress Code Interested?! Apply TODAY! You can also call/text me, Olivia Sloane, at and send an updated resume to with the best time and phone number for me to reach you as well! You can also schedule an appointment with my calendar: Olivia Sloane Client Relationship Manager & Senior Healthcare Recruiter, K.A. Recruiting, Inc.
NEW Cytotechnologist Opening (Permanent Full Time Onsite Position) Join a fast-paced diagnostic laboratory that specializes in advanced molecular testing, including PCR-based diagnostics , with a focus on gynecology, infectious diseases, tick-borne illnesses, mycology, and chronic fatigue syndrome (CFS) . Currently seeking a Cytotechnologist to support high-quality specimen screening and evaluation. Position Summary: As a Cytotechnologist , you will play a critical role in identifying cellular abnormalities and assisting pathologists in making timely and accurate diagnoses. You'll perform both gynecological and non-gynecological microscopic evaluations , ensuring quality and precision throughout. Key Responsibilities: Perform microscopic screening of cellular samples using established cytological criteria Document specimen evaluations and ensure proper turnaround time Collaborate with supervisory cytotechnologists and pathologists for result correlation Maintain lab safety protocols and equipment Prepare high-quality cytology slides using approved laboratory methods Ensure patient confidentiality and data accuracy Contribute to team efforts with initiative and accountability Qualifications: Bachelor s degree in a related science field ASCP Board Certification required All levels of experience accepted (new grads encouraged to apply) Experience with ThinPrep Imaging System and Review Scope is a plus What We Offer: Competitive salary based on experience Full range of benefits: Medical, Dental & Vision Insurance Short & Long Term Disability, Life Insurance Flexible Spending Accounts & Voluntary Insurance Options Identity Theft Protection 401(k) Retirement Plan Paid Vacation & Holidays Business Casual Dress Code Interested?! Apply TODAY! You can also call/text me, Olivia Sloane, at and send an updated resume to with the best time and phone number for me to reach you as well! You can also schedule an appointment with my calendar: Olivia Sloane Client Relationship Manager & Senior Healthcare Recruiter, K.A. Recruiting, Inc.
12/10/2025
Full time
NEW Cytotechnologist Opening (Permanent Full Time Onsite Position) Join a fast-paced diagnostic laboratory that specializes in advanced molecular testing, including PCR-based diagnostics , with a focus on gynecology, infectious diseases, tick-borne illnesses, mycology, and chronic fatigue syndrome (CFS) . Currently seeking a Cytotechnologist to support high-quality specimen screening and evaluation. Position Summary: As a Cytotechnologist , you will play a critical role in identifying cellular abnormalities and assisting pathologists in making timely and accurate diagnoses. You'll perform both gynecological and non-gynecological microscopic evaluations , ensuring quality and precision throughout. Key Responsibilities: Perform microscopic screening of cellular samples using established cytological criteria Document specimen evaluations and ensure proper turnaround time Collaborate with supervisory cytotechnologists and pathologists for result correlation Maintain lab safety protocols and equipment Prepare high-quality cytology slides using approved laboratory methods Ensure patient confidentiality and data accuracy Contribute to team efforts with initiative and accountability Qualifications: Bachelor s degree in a related science field ASCP Board Certification required All levels of experience accepted (new grads encouraged to apply) Experience with ThinPrep Imaging System and Review Scope is a plus What We Offer: Competitive salary based on experience Full range of benefits: Medical, Dental & Vision Insurance Short & Long Term Disability, Life Insurance Flexible Spending Accounts & Voluntary Insurance Options Identity Theft Protection 401(k) Retirement Plan Paid Vacation & Holidays Business Casual Dress Code Interested?! Apply TODAY! You can also call/text me, Olivia Sloane, at and send an updated resume to with the best time and phone number for me to reach you as well! You can also schedule an appointment with my calendar: Olivia Sloane Client Relationship Manager & Senior Healthcare Recruiter, K.A. Recruiting, Inc.
NEW Cytotechnologist Opening (Permanent Full Time Onsite Position) Join a fast-paced diagnostic laboratory that specializes in advanced molecular testing, including PCR-based diagnostics , with a focus on gynecology, infectious diseases, tick-borne illnesses, mycology, and chronic fatigue syndrome (CFS) . Currently seeking a Cytotechnologist to support high-quality specimen screening and evaluation. Position Summary: As a Cytotechnologist , you will play a critical role in identifying cellular abnormalities and assisting pathologists in making timely and accurate diagnoses. You'll perform both gynecological and non-gynecological microscopic evaluations , ensuring quality and precision throughout. Key Responsibilities: Perform microscopic screening of cellular samples using established cytological criteria Document specimen evaluations and ensure proper turnaround time Collaborate with supervisory cytotechnologists and pathologists for result correlation Maintain lab safety protocols and equipment Prepare high-quality cytology slides using approved laboratory methods Ensure patient confidentiality and data accuracy Contribute to team efforts with initiative and accountability Qualifications: Bachelor s degree in a related science field ASCP Board Certification required All levels of experience accepted (new grads encouraged to apply) Experience with ThinPrep Imaging System and Review Scope is a plus What We Offer: Competitive salary based on experience Full range of benefits: Medical, Dental & Vision Insurance Short & Long Term Disability, Life Insurance Flexible Spending Accounts & Voluntary Insurance Options Identity Theft Protection 401(k) Retirement Plan Paid Vacation & Holidays Business Casual Dress Code Interested?! Apply TODAY! You can also call/text me, Olivia Sloane, at and send an updated resume to with the best time and phone number for me to reach you as well! You can also schedule an appointment with my calendar: Olivia Sloane Client Relationship Manager & Senior Healthcare Recruiter, K.A. Recruiting, Inc.
12/10/2025
Full time
NEW Cytotechnologist Opening (Permanent Full Time Onsite Position) Join a fast-paced diagnostic laboratory that specializes in advanced molecular testing, including PCR-based diagnostics , with a focus on gynecology, infectious diseases, tick-borne illnesses, mycology, and chronic fatigue syndrome (CFS) . Currently seeking a Cytotechnologist to support high-quality specimen screening and evaluation. Position Summary: As a Cytotechnologist , you will play a critical role in identifying cellular abnormalities and assisting pathologists in making timely and accurate diagnoses. You'll perform both gynecological and non-gynecological microscopic evaluations , ensuring quality and precision throughout. Key Responsibilities: Perform microscopic screening of cellular samples using established cytological criteria Document specimen evaluations and ensure proper turnaround time Collaborate with supervisory cytotechnologists and pathologists for result correlation Maintain lab safety protocols and equipment Prepare high-quality cytology slides using approved laboratory methods Ensure patient confidentiality and data accuracy Contribute to team efforts with initiative and accountability Qualifications: Bachelor s degree in a related science field ASCP Board Certification required All levels of experience accepted (new grads encouraged to apply) Experience with ThinPrep Imaging System and Review Scope is a plus What We Offer: Competitive salary based on experience Full range of benefits: Medical, Dental & Vision Insurance Short & Long Term Disability, Life Insurance Flexible Spending Accounts & Voluntary Insurance Options Identity Theft Protection 401(k) Retirement Plan Paid Vacation & Holidays Business Casual Dress Code Interested?! Apply TODAY! You can also call/text me, Olivia Sloane, at and send an updated resume to with the best time and phone number for me to reach you as well! You can also schedule an appointment with my calendar: Olivia Sloane Client Relationship Manager & Senior Healthcare Recruiter, K.A. Recruiting, Inc.
LabCorp is seeking a Molecular Technologist Trainee to join their Molecular Diagnostics team in Westborough, MA! They will be responsible for performing complex molecular testing and results analysis according to established standard operating procedures. The Integrated Genetics-Westborough site processes extracted DNA from peripheral blood and prenatal samples (amniotic fluid and chorionic villi) for genetic testing. A variety of molecular genetics techniques are used to include Next Generation Sequencing, real time PCR, Sanger Sequencing and Southern Blot analysis to test for specific genetic diseases such as cystic fibrosis, spinal muscular atrophy and Fragile X syndrome to name just a few. Pay Range: $26.00 - $36.00 per hour All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data Work Schedule: Monday-Friday 3:00pm-11:30pm Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here . Job Responsibilities Perform complex molecular-based procedures, including NGS, with a high degree of quality and in accordance to established protocols Maintain complete documentation for all steps of the processes per the SOPs Prepare the appropriate reagents for all required testing Analyze and interpret patient test results in a timely manner Participate in the training of other technologists when requested Troubleshoot assays and reagent qualification issues Participate in verification and validation studies for process improvements, new equipment and technology transfers in the laboratory Take on independent projects and tasks beyond routine work Contribute to ongoing process improvement efforts Requirements Bachelor's degree in Chemical or Biological science, Clinical Laboratory Science, Medical Technology or a non-traditional Bachelor's degree that meets local regulatory (CLIA & State) requirements Previous clinical laboratory testing experience is not required Prior experience performing molecular techniques, such as DNA extraction, PCR, sequencing, NGS, genotyping is highly desired ASCP or AMT certification is preferred Strong understanding of molecular genetics and general chemistry Previous molecular biology lab experience highly preferred Ability to work independently and within a team environment Proficient with computers; Familiarity with laboratory information systems are a plus High level of attention detail along with strong communication and organizational skills Must be able to pass a standardized color vision screen Flexibility to work overtime or other shifts depending on business needs If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today! Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. A dditionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement .
12/09/2025
Full time
LabCorp is seeking a Molecular Technologist Trainee to join their Molecular Diagnostics team in Westborough, MA! They will be responsible for performing complex molecular testing and results analysis according to established standard operating procedures. The Integrated Genetics-Westborough site processes extracted DNA from peripheral blood and prenatal samples (amniotic fluid and chorionic villi) for genetic testing. A variety of molecular genetics techniques are used to include Next Generation Sequencing, real time PCR, Sanger Sequencing and Southern Blot analysis to test for specific genetic diseases such as cystic fibrosis, spinal muscular atrophy and Fragile X syndrome to name just a few. Pay Range: $26.00 - $36.00 per hour All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data Work Schedule: Monday-Friday 3:00pm-11:30pm Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here . Job Responsibilities Perform complex molecular-based procedures, including NGS, with a high degree of quality and in accordance to established protocols Maintain complete documentation for all steps of the processes per the SOPs Prepare the appropriate reagents for all required testing Analyze and interpret patient test results in a timely manner Participate in the training of other technologists when requested Troubleshoot assays and reagent qualification issues Participate in verification and validation studies for process improvements, new equipment and technology transfers in the laboratory Take on independent projects and tasks beyond routine work Contribute to ongoing process improvement efforts Requirements Bachelor's degree in Chemical or Biological science, Clinical Laboratory Science, Medical Technology or a non-traditional Bachelor's degree that meets local regulatory (CLIA & State) requirements Previous clinical laboratory testing experience is not required Prior experience performing molecular techniques, such as DNA extraction, PCR, sequencing, NGS, genotyping is highly desired ASCP or AMT certification is preferred Strong understanding of molecular genetics and general chemistry Previous molecular biology lab experience highly preferred Ability to work independently and within a team environment Proficient with computers; Familiarity with laboratory information systems are a plus High level of attention detail along with strong communication and organizational skills Must be able to pass a standardized color vision screen Flexibility to work overtime or other shifts depending on business needs If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today! Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. A dditionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement .
Sign-on Bonus $5,000 The Histotechnologist I is accountable for the histology handling/storing of precious clinical trial specimens. The Histotechnologist supports the various teams of the Specimen Management Center and is a liaison between Specimen Management and others departments. The Histotechnologist will actively liaise with the CCLS project management team, Investigator Support Team and client to resolve and clarify questions and/ or issues related to management and preparation of the histology samples. Shift: Monday-Friday 2pm-10:30pm, possible Saturday rotation as needed Work Location: 8211 Scicor Drive Indianapolis, IN 46254 Pay Range: All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here . Essential Job Duties: Specific department duties as set forth in the task list and/or department training checklists including but not limited to: Utilize knowledge and experience with histology samples to maintain proper storage conditions and facilitate accessioning of blocks and slides (stained and unstained). Routine decalcification, processing, embedding, microtomy and re-embedding of human tissue specimens from patients enrolled in clinical trials. Perform routine, special stains, and advanced staining assays according to SOPs, protocols, and in line with global and regional regulatory requirements. Perform slide scanning as required and according to protocols. Ensure that Special Handling specimens are picked up from the appropriate area, sorted, accessioned, pre-scanned and registered into the appropriate temperature bins in a timely fashion. Generation and application of specialized labels to include aliquot and/or mini labels with client specific elements. General duties including but not limited to: Resolve pendings. Retrieve and check specimens against pending list. Document specimen discrepancies. Notify laboratory management when specimen discrepancies are not resolved. Prepare workstation, instrumentation and maintenance on instruments and/or equipment daily, weekly, monthly, quarterly and annually. Ability to adequately maintain accurate records and both adhere to Standard Operating Procedures: Calibrate instruments, verification of temperature, and logging of data as required. Ensure that maintenance is performed and documented according to SOP. Perform basic instrument and/or equipment troubleshooting. Document corrective actions for unusual occurrences. Notify management when an instrument and/or equipment does not meet specifications. Ability to use different application software. Document quality control results. Perform proficiency testing survey as patient specimens. Reagents, material and supplies monitoring: Order, receive, open and place in service all reagents/material according to SOPs. Document implementation of new reagents/material according to SOPs. Perform lot-to-lot comparison according to SOPS. Perform inventory and checks of reagents/material. Adheres to all company policies and procedures and performs all departmental and interdepartmental SOP's as written. Adheres to safety and occupational health policies and standards. Training Required Experience: At least 6 months experience in histology laboratory setting unless HS educated with ASCP certification. • Able to work in a team as well as independently • Dynamic attitude and ability to work under pressure • Ability to take up challenges • Strong detail orientation • Strong verbal and written communication and organizational skills • Ability to use several software packages i.e., Word, Excel, Visio • Ability to adequately maintain accurate records and both adhere to and author Standard Operating Procedures. • Able to troubleshoot problems with automated histological equipment. Requires theoretical and practical knowledge of histology and processing of human tissue specimens, including handling and storage of histology samples. • Candidate must have the knowledge of molecular histology and techniques, including immunohistochemistry and FISH. • Candidate must be familiar with labeling and accessioning procedures and tracking of paraffin tissue blocks and slides. Education/Qualifications/Certifications and Licenses Individual must qualify as testing personnel under the following CAP/CLIA 1988 and New York State Department of Health requirements: Currently certified as a Histotechnician by the American Society for Clinical Pathology (ASCP) Board of Certification with the ASCP (HT/HTL) or ASCPi (HT) credential OR Bachelor's degree from a regionally accredited college/university with a combination of 30 semester hours (45 quarter hours) of biology and chemistry (must include credit hours in both) AND successful completion of a course of training of at least nine months in an Histotechnician program from an accredited institution OR Bachelor's degree from a regionally accredited college/university with a combination of 30 semester hours (45 quarter hours) of biology and chemistry (must include credits hours in both) AND one year of experience and/or training in histology within the past 5 years, under the direction of a pathologist certified by the American Board of Pathology in anatomic pathology OR Successful completion of a course of study that meets all academic requirements for an associates, or higher, degree in a Histotechnician program from an accredited institution. OR Associate's degree, or higher, in one of the chemical, physical or biological sciences from a regionally accredited college/university AND one year of experience and/or training in histology within the past 5 years, under the direction of a pathologist certified by the American Board of Pathology in anatomic pathology. OR Associate's degree, or higher, in one of the chemical, physical or biological sciences from a regionally accredited college/university AND successful completion of a course of training of at least nine months in a Histotechnician program from an accredited institution. Working Conditions: Repetitive motion via samples and computer terminal High volume and high production environment Constant exposure to dangerous goods and infectious substance Exposure to extreme temperatures Exposure to 10% Neutral Buffered Formalin and other common histology chemicals Work with other potentially hazardous substances not limited to known/potential teratogens or carcinogens test materials Adhere to established LabCorp safety SOP's and Universal Precautions guidelines at all times Rotation Tuesday-Saturday or Monday-Friday may be required Overtime may be required High volume and high production environment Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. A dditionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement .
12/09/2025
Full time
Sign-on Bonus $5,000 The Histotechnologist I is accountable for the histology handling/storing of precious clinical trial specimens. The Histotechnologist supports the various teams of the Specimen Management Center and is a liaison between Specimen Management and others departments. The Histotechnologist will actively liaise with the CCLS project management team, Investigator Support Team and client to resolve and clarify questions and/ or issues related to management and preparation of the histology samples. Shift: Monday-Friday 2pm-10:30pm, possible Saturday rotation as needed Work Location: 8211 Scicor Drive Indianapolis, IN 46254 Pay Range: All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here . Essential Job Duties: Specific department duties as set forth in the task list and/or department training checklists including but not limited to: Utilize knowledge and experience with histology samples to maintain proper storage conditions and facilitate accessioning of blocks and slides (stained and unstained). Routine decalcification, processing, embedding, microtomy and re-embedding of human tissue specimens from patients enrolled in clinical trials. Perform routine, special stains, and advanced staining assays according to SOPs, protocols, and in line with global and regional regulatory requirements. Perform slide scanning as required and according to protocols. Ensure that Special Handling specimens are picked up from the appropriate area, sorted, accessioned, pre-scanned and registered into the appropriate temperature bins in a timely fashion. Generation and application of specialized labels to include aliquot and/or mini labels with client specific elements. General duties including but not limited to: Resolve pendings. Retrieve and check specimens against pending list. Document specimen discrepancies. Notify laboratory management when specimen discrepancies are not resolved. Prepare workstation, instrumentation and maintenance on instruments and/or equipment daily, weekly, monthly, quarterly and annually. Ability to adequately maintain accurate records and both adhere to Standard Operating Procedures: Calibrate instruments, verification of temperature, and logging of data as required. Ensure that maintenance is performed and documented according to SOP. Perform basic instrument and/or equipment troubleshooting. Document corrective actions for unusual occurrences. Notify management when an instrument and/or equipment does not meet specifications. Ability to use different application software. Document quality control results. Perform proficiency testing survey as patient specimens. Reagents, material and supplies monitoring: Order, receive, open and place in service all reagents/material according to SOPs. Document implementation of new reagents/material according to SOPs. Perform lot-to-lot comparison according to SOPS. Perform inventory and checks of reagents/material. Adheres to all company policies and procedures and performs all departmental and interdepartmental SOP's as written. Adheres to safety and occupational health policies and standards. Training Required Experience: At least 6 months experience in histology laboratory setting unless HS educated with ASCP certification. • Able to work in a team as well as independently • Dynamic attitude and ability to work under pressure • Ability to take up challenges • Strong detail orientation • Strong verbal and written communication and organizational skills • Ability to use several software packages i.e., Word, Excel, Visio • Ability to adequately maintain accurate records and both adhere to and author Standard Operating Procedures. • Able to troubleshoot problems with automated histological equipment. Requires theoretical and practical knowledge of histology and processing of human tissue specimens, including handling and storage of histology samples. • Candidate must have the knowledge of molecular histology and techniques, including immunohistochemistry and FISH. • Candidate must be familiar with labeling and accessioning procedures and tracking of paraffin tissue blocks and slides. Education/Qualifications/Certifications and Licenses Individual must qualify as testing personnel under the following CAP/CLIA 1988 and New York State Department of Health requirements: Currently certified as a Histotechnician by the American Society for Clinical Pathology (ASCP) Board of Certification with the ASCP (HT/HTL) or ASCPi (HT) credential OR Bachelor's degree from a regionally accredited college/university with a combination of 30 semester hours (45 quarter hours) of biology and chemistry (must include credit hours in both) AND successful completion of a course of training of at least nine months in an Histotechnician program from an accredited institution OR Bachelor's degree from a regionally accredited college/university with a combination of 30 semester hours (45 quarter hours) of biology and chemistry (must include credits hours in both) AND one year of experience and/or training in histology within the past 5 years, under the direction of a pathologist certified by the American Board of Pathology in anatomic pathology OR Successful completion of a course of study that meets all academic requirements for an associates, or higher, degree in a Histotechnician program from an accredited institution. OR Associate's degree, or higher, in one of the chemical, physical or biological sciences from a regionally accredited college/university AND one year of experience and/or training in histology within the past 5 years, under the direction of a pathologist certified by the American Board of Pathology in anatomic pathology. OR Associate's degree, or higher, in one of the chemical, physical or biological sciences from a regionally accredited college/university AND successful completion of a course of training of at least nine months in a Histotechnician program from an accredited institution. Working Conditions: Repetitive motion via samples and computer terminal High volume and high production environment Constant exposure to dangerous goods and infectious substance Exposure to extreme temperatures Exposure to 10% Neutral Buffered Formalin and other common histology chemicals Work with other potentially hazardous substances not limited to known/potential teratogens or carcinogens test materials Adhere to established LabCorp safety SOP's and Universal Precautions guidelines at all times Rotation Tuesday-Saturday or Monday-Friday may be required Overtime may be required High volume and high production environment Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. A dditionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement .
POSITION SUMMARY/RESPONSIBILITIES To provide expert, advanced technical skills necessary to organize and perform general supervision and histocompatibility testing for organ and stem transplantation, platelet transfusion and disease risk analysis; and chimerism/monitoring engraftment. Responsible for supervising and performing HLA antibody analysis, flow cross matching, molecular tissue typing, molecular chimerism analysis and other histocompatibility testing procedures. Performs assigned duties rapidly and accurately. Plans work activities and makes decisions connected with own work and provides guidance to other staff members in these areas. Recognizes unusual results and/or abnormalities and takes prompt and appropriate action to assure the accuracy and validity of test results. Assumes accountability for the dissemination of patient information to ensure the confidentiality and privacy of patients. Duties may also include performance of procedures associated with procurement of blood specimens from patients, donors and control subjects. EDUCATION/EXPERIENCE Bachelor's degree in medical technology or an appropriate biological/chemical/medical science from an accredited college or university is required. Certifications as a Histocompatibility Technologist is highly recommended. Three years of histocompatibility testing experience is required with a performance record indicating exceptional initiative and competency in performance of all laboratory test procedures currently offered.
12/08/2025
Full time
POSITION SUMMARY/RESPONSIBILITIES To provide expert, advanced technical skills necessary to organize and perform general supervision and histocompatibility testing for organ and stem transplantation, platelet transfusion and disease risk analysis; and chimerism/monitoring engraftment. Responsible for supervising and performing HLA antibody analysis, flow cross matching, molecular tissue typing, molecular chimerism analysis and other histocompatibility testing procedures. Performs assigned duties rapidly and accurately. Plans work activities and makes decisions connected with own work and provides guidance to other staff members in these areas. Recognizes unusual results and/or abnormalities and takes prompt and appropriate action to assure the accuracy and validity of test results. Assumes accountability for the dissemination of patient information to ensure the confidentiality and privacy of patients. Duties may also include performance of procedures associated with procurement of blood specimens from patients, donors and control subjects. EDUCATION/EXPERIENCE Bachelor's degree in medical technology or an appropriate biological/chemical/medical science from an accredited college or university is required. Certifications as a Histocompatibility Technologist is highly recommended. Three years of histocompatibility testing experience is required with a performance record indicating exceptional initiative and competency in performance of all laboratory test procedures currently offered.
Job Title: ASCP Molecular Technologist Location: Houston, TX Hourly Rate: $30-50 per hour We are currently seeking multiple ASCP Molecular Technologists to join our team in Houston. This exciting opportunity offers a competitive hourly rate within the range of $30-50 per hour. Key Responsibilities: Perform molecular testing procedures according to established protocols Operate and maintain laboratory equipment Analyze and report results with accuracy Adhere to quality control and quality assurance protocols Maintain laboratory records and documentation Qualifications: ASCP certification as a Molecular Technologist Prior experience in molecular testing techniques Strong attention to detail and accuracy Excellent communication and teamwork skills Ability to work independently and in a team environment If you meet the qualifications and are looking for a rewarding opportunity in the field of molecular testing, we encourage you to apply for the ASCP Molecular Technologist position in Houston today. Apply to this ad, or email your resume to You can also call/text
12/04/2025
Full time
Job Title: ASCP Molecular Technologist Location: Houston, TX Hourly Rate: $30-50 per hour We are currently seeking multiple ASCP Molecular Technologists to join our team in Houston. This exciting opportunity offers a competitive hourly rate within the range of $30-50 per hour. Key Responsibilities: Perform molecular testing procedures according to established protocols Operate and maintain laboratory equipment Analyze and report results with accuracy Adhere to quality control and quality assurance protocols Maintain laboratory records and documentation Qualifications: ASCP certification as a Molecular Technologist Prior experience in molecular testing techniques Strong attention to detail and accuracy Excellent communication and teamwork skills Ability to work independently and in a team environment If you meet the qualifications and are looking for a rewarding opportunity in the field of molecular testing, we encourage you to apply for the ASCP Molecular Technologist position in Houston today. Apply to this ad, or email your resume to You can also call/text
Description Summary: Performs all lab assistant procedures (including, but not limited to, phlebotomy, client processing, and client services representative functions) and oversees such staff under the guidelines and supervision of the assigned Leader to assure appropriate patient care is met. Responsible for monitoring, rotating stock, or requesting general laboratory and phlebotomy supplies as needed. Assists in specimen processing/handling, collection, and designated testing functions in all areas of the lab. Responsibilities: Meets expectations of the applicable OneCHRISTUS Competencies: Leader of Self, Leader of Others, or Leader of Leaders. Customer Service / AIDET / Standards of Behavior. Trains and performs competency checklist with all Phlebotomist/ laboratory assistant staff. Monitors the collection report; resolves problems; completes related paperwork and computer functions. Uses centrifuge, prepares and assures serum/blood specimens are acceptable; prepares specimen for referral to outside reference laboratories; dispenses blood products under supervision of medical technologist. Monitoring the collection area continuously during the shift to assure that all specimens are collected within a timely manner and assisting the phlebotomists in obtaining specimens, if necessary. Handling inquiries, questions and problems as they arise, both within the laboratory and between the lab and other departments in the hospital, maintaining a professional image and exhibiting excellent service. Greets all customers, clients, outpatients, and visitors physically or on the telephone; provides accurate, appropriate, and courteous response to technical questions and results inquiry as requested by physicians and nursing personnel. Communicating follow-up information regarding patient care issues or physician related complaints to the appropriate supervisor, manager, charge tech or director. Performs clerical office duties, client processing, and client service representative duties, as assigned/required. Enters orders and cancellations using Hospital LIS. Receives and processes specimens collected and/or add-on tests and distributes them to the appropriate departments. Processes and maintains laboratory records and reports; monitors chart print rounds for completion and processes reports for Health Information, faxes or mails reports as requested by physicians or clients, processes reference reports, resolves all pending transactions, and maintains printers, copier, and fax machine. Specimen collections are initiated within the appropriate response time. Monitors the collections pending. Reports and resolves problems, completes related paperwork and computer functions. Works as a team member to perform and complete all patient related testing/reporting regardless of individual assignments, to provide timely results on a daily basis. Completes tasks or special projects within the time frame, allowed per any guidelines established as assigned by laboratory supervisory personnel. Inventory control - monitors supply receiving area, distributes supplies, restocks, and processes packing slips; notifies appropriate supervisor/manager when instrument parts, reagents, or supplies are at reorder levels; dates reagents when received and opened according to laboratory policy, and notifies supervisor of expired reagents; completes supply orders, as assigned. Practices safety, infection control, and security as defined by the hospital department and section policy and procedure manuals; follows all safety and infection control procedures including wearing appropriate PPE for assigned job functions; disposes of biohazardous materials and hazardous chemicals as established by departmental policy; all patient information, including lab results, are maintained in the strictest of confidence, limited to health care professionals needing this information to perform patient care. Demonstrates work schedule flexibility by willingly rotating shifts and changing assignments, as required. Job Requirements: Education/Skills Associate of Science Degree preferred. Basic knowledge in the areas of microbiology, immunology or molecular biology and biochemistry as related to infectious diseases required. Experience 2 years of experience as a Phlebotomist or Laboratory Assistant in a clinical laboratory setting required 5+ years of experience preferred. Licenses, Registrations, or Certifications Medical Laboratory Assistant Certification or Phlebotomist Certification - PBT (ASCP), RPT (AMT), CPT (NPA) or equivalent required. Louisiana requires State Licensure. Work Schedule: 7PM - 7AM Work Type: Full Time
12/02/2025
Full time
Description Summary: Performs all lab assistant procedures (including, but not limited to, phlebotomy, client processing, and client services representative functions) and oversees such staff under the guidelines and supervision of the assigned Leader to assure appropriate patient care is met. Responsible for monitoring, rotating stock, or requesting general laboratory and phlebotomy supplies as needed. Assists in specimen processing/handling, collection, and designated testing functions in all areas of the lab. Responsibilities: Meets expectations of the applicable OneCHRISTUS Competencies: Leader of Self, Leader of Others, or Leader of Leaders. Customer Service / AIDET / Standards of Behavior. Trains and performs competency checklist with all Phlebotomist/ laboratory assistant staff. Monitors the collection report; resolves problems; completes related paperwork and computer functions. Uses centrifuge, prepares and assures serum/blood specimens are acceptable; prepares specimen for referral to outside reference laboratories; dispenses blood products under supervision of medical technologist. Monitoring the collection area continuously during the shift to assure that all specimens are collected within a timely manner and assisting the phlebotomists in obtaining specimens, if necessary. Handling inquiries, questions and problems as they arise, both within the laboratory and between the lab and other departments in the hospital, maintaining a professional image and exhibiting excellent service. Greets all customers, clients, outpatients, and visitors physically or on the telephone; provides accurate, appropriate, and courteous response to technical questions and results inquiry as requested by physicians and nursing personnel. Communicating follow-up information regarding patient care issues or physician related complaints to the appropriate supervisor, manager, charge tech or director. Performs clerical office duties, client processing, and client service representative duties, as assigned/required. Enters orders and cancellations using Hospital LIS. Receives and processes specimens collected and/or add-on tests and distributes them to the appropriate departments. Processes and maintains laboratory records and reports; monitors chart print rounds for completion and processes reports for Health Information, faxes or mails reports as requested by physicians or clients, processes reference reports, resolves all pending transactions, and maintains printers, copier, and fax machine. Specimen collections are initiated within the appropriate response time. Monitors the collections pending. Reports and resolves problems, completes related paperwork and computer functions. Works as a team member to perform and complete all patient related testing/reporting regardless of individual assignments, to provide timely results on a daily basis. Completes tasks or special projects within the time frame, allowed per any guidelines established as assigned by laboratory supervisory personnel. Inventory control - monitors supply receiving area, distributes supplies, restocks, and processes packing slips; notifies appropriate supervisor/manager when instrument parts, reagents, or supplies are at reorder levels; dates reagents when received and opened according to laboratory policy, and notifies supervisor of expired reagents; completes supply orders, as assigned. Practices safety, infection control, and security as defined by the hospital department and section policy and procedure manuals; follows all safety and infection control procedures including wearing appropriate PPE for assigned job functions; disposes of biohazardous materials and hazardous chemicals as established by departmental policy; all patient information, including lab results, are maintained in the strictest of confidence, limited to health care professionals needing this information to perform patient care. Demonstrates work schedule flexibility by willingly rotating shifts and changing assignments, as required. Job Requirements: Education/Skills Associate of Science Degree preferred. Basic knowledge in the areas of microbiology, immunology or molecular biology and biochemistry as related to infectious diseases required. Experience 2 years of experience as a Phlebotomist or Laboratory Assistant in a clinical laboratory setting required 5+ years of experience preferred. Licenses, Registrations, or Certifications Medical Laboratory Assistant Certification or Phlebotomist Certification - PBT (ASCP), RPT (AMT), CPT (NPA) or equivalent required. Louisiana requires State Licensure. Work Schedule: 7PM - 7AM Work Type: Full Time
