Laboratory scientist jobs in White Plains, New YorkCreate job alerts

Job Description Melissa Owens| President P: (386)339-0839 |E: melissa@alliedsearchpartners.com Schedule a Meeting: https://calendly.com/melissaowens Allied Search Partners Allied Search Partners is back by two decades of healthcare staffing excellence. We are a trusted healthcare staffing firm supporting medical and dental offices nationwide. We partner with private practices and corporate healthcare organizations to provide reliable, well-supported temporary professionals—while prioritizing fair pay, consistency, and respect for our workers’ time. Our team offers 24/7 scheduling support and access to shifts through our efficient temp scheduling application. Unlike traditional staffing agencies that push one-off shifts to large candidate pools, we focus on long-term relationships with both our healthcare facilities and our workers. Job Description Job ID: 3563480 Job Title: Histotechnician Location: South Westchester County, NY Shift: • Per Diem: Varied, • Full Time: Monday to Friday 2pm to 10pm Job Summary: Performs Histological technical procedures using manual and automated techniques to achieve high-quality Pathology slides for review by Pathologists. Job Responsibilities: If Clinical Laboratory Scientist • Understands and adheres to the performance standards, policies, and behaviors, • Laboratory testing personnel responsibilities include:, • Following the laboratory’s pre-analytic and analytic procedures and maintaining records of these tests, • Maintaining records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens, • Adhering to the laboratory’s quality assurance procedures, including documenting all:, • Quality control activities including quality control testing and calibrations, • Instrument and equipment verifications, • Maintenance and preventative maintenance, • Following the laboratory’s policies and procedures whenever test systems are not within the laboratory’s established performance specifications, • Identifying and documenting problems that may adversely affect test performance and notifying the supervisor, assistant director or director and documenting all corrective actions taken when test systems deviate from the laboratory’s established performance specifications, • Ensures the accuracy and quality of all results from pre-analytic, analytic, and post-analytic phases of testing., • Notifies and documents clinicians and patient units of all critical values and maintains the laboratory STAT turn around time requirements., • Participates in regulatory readiness for CAP, AABB, NYSDOH, and Joint Commission., • Maintains 12 Continuing Education credits per year., • Understands and participates in standard operating procedures, proficiency testing, inspection audits, quality program including reporting non-conformances., • Evaluates test results for abnormalities and confirms those results per department protocols where required., • Participates in validations, training, and competency assessments as required., • Responsible for inventory management of lot numbers, expiration dates, labeling, and QC requirement., • Completes all annual mandatory training, in-services, and ongoing education as required., • Performs other duties as assigned., • Section testing training and competency assessments are maintained by the section laboratory supervisor for all assigned disciplines If Histotechnician: • Understands and adheres to the Performance Standards, Policies and Behaviors., • Performs all other related duties as assigned., • Performs embedding and sectioning of tissue blocks following section protocol as to biopsies, routine, etc., • Evaluates routine stain daily (H&E), reviews for inconsistencies and confirms and/or corrects before releasing slides., • Performs Special Stains and evaluates for inconsistencies and confirms and/or correct before releasing slides, Checks positive controls and documents on run log(s)., • Performs Immunohistochemistry, and evaluates for inconsistencies and confirms and/or correct before releasing slides, Checks positive and negative controls and documents on run log(s). Qualifications: If Clinical Laboratory Scientist • Current NYS License as a Clinical Laboratory Technologist, NYS PA License required., • Education in accordance with the NYS Office of Professions and CLIA requirements of testing personnel., • Preferred with ASCP Certification. If Histotechnician • NYS Clinical Laboratory Technician License or NYS histotechnician license required., • Degree in Medical Technology or related science preferred with one year of relevant hospital experience in Histology., • ASCP preferred Core Competencies: • Flexibility, • Organized, • Adaptability, • Attention to Detail, • Stress Tolerance Work Environment: May be exposed to chemicals necessary to perform required tasks. Any hazardous chemicals the employee may be exposed to are listed in the hospital’s SDS (Safety Data Sheet) data base and may be accessed through the hospital’s Intranet site (Employee Tools/SDS Access). A copy of the SDS data base can also be found at the hospital switchboard, saved on a disc. Required Skill: • Must be able to remain stationary for extended/prolonged periods, • Must be able to constantly operate computer, equipment and other devices, • Position requires ability to concentrate on fine detail with interruptions and attend to tasks for more than sixty (60) minutes at a time. Note: The responsibilities and tasks outlined in this job description are not exhaustive and may change as determined by the needs hospital.

Job DescriptionClinical Lab Scientist / HistotechnicianRole Summary Join a high-precision diagnostic team dedicated to clinical excellence and patient safety. Whether functioning as a Clinical Laboratory Scientist (CLS) or a Histotechnician, you will play a vital role in the diagnostic process. Histotechnicians will utilize both manual and automated techniques to produce high-quality pathology slides, while Clinical Lab Scientists will oversee the accuracy and quality of results across all phases of testing. This is an inspiring opportunity for a detail-oriented professional to contribute to a life-saving laboratory environment that values continuous learning and rigorous quality standards. Key Duties: Laboratory Operations (CLS): Follow pre-analytic and analytic procedures, maintaining meticulous records for proficiency testing and patient specimens. Histological Excellence (Histo): Perform embedding and sectioning of tissue blocks. Evaluate routine (H&E), special, and immunohistochemistry stains for accuracy before releasing slides. Quality Assurance: Adhere to all quality control activities, calibrations, and equipment verifications. Identify and document any deviations from performance specifications. Regulatory Compliance: Participate in regulatory readiness for CAP, AABB, NYSDOH, and the Joint Commission. Ensure all testing meets CLIA requirements. Clinical Collaboration: Confirm and communicate critical values to clinicians and patient units while maintaining strict STAT turnaround times. Inventory & Maintenance: Manage lot numbers, expiration dates, and labeling. Perform preventative maintenance on laboratory instrumentation. Continuous Growth: Participate in validations, training, and competency assessments, maintaining at least 12 continuing education credits per year. Required Qualifications For CLS Candidates: * Current NYS License as a Clinical Laboratory Technologist or NYS PA License. Education in accordance with NYS Office of Professions and CLIA testing personnel requirements. For Histotechnician Candidates: * NYS Clinical Laboratory Technician License or NYS Histotechnician License. Health & Safety: Flu Vaccine required (No exceptions). Skills: Proficiency in adhering to performance standards, policies, and professional behaviors in a laboratory setting. Desired Qualifications Certification: ASCP Certification is highly preferred for both roles. Education (Histo): Degree in Medical Technology or a related science preferred. Experience (Histo): One year of relevant hospital experience in Histology is preferred. Location and Work Type Setting: Hospital Laboratory Location: White Plains, NY Work Type: Full-Time | Direct Hire Schedule: Varied shifts available; Monday – Friday (9:00 AM – 5:00 PM or 2:00 PM – 10:00 PM). Total Rewards: Full suite of healthcare benefits and a robust retirement plan. If you're interested, please reply to this advertisement or directly email your resume to me at DSalgado@teemagroup.com or by calling/texting (949) 295-5951. I strive to reply within 48 hours. Looking forward to connecting with you soon. Thank you!

Job Description Job Title: Associate Scientist – Embryology Book here for more information: https://talentassistant.actalentservices.com/assistant/bookings/BfUTMTxl This temporary Associate Scientist, Embryology role focuses on developing and applying innovative assisted reproductive and genetic engineering technologies to generate genetically engineered animal models that support drug discovery. The position prepares and manipulates embryos and gametes, introduces genetic modifications using appropriate methods, and supports cohort generation through advanced assisted reproductive technologies. The Associate Scientist works closely with a multidisciplinary project team, independently executes complex experimental procedures, and contributes to the design, execution, analysis, and interpretation of experiments while staying current with advances in embryology, reproductive biology, and transgenic technologies. Responsibilities • Prepare staged embryos or gametes for manipulation using established and emerging laboratory techniques., • Introduce genetic modifications into embryos or gametes using appropriate gene editing and related methods., • Transfer manipulated or in vitro fertilization (IVF)-derived embryos into recipient females to generate experimental cohorts., • Support cohort generation and preservation by applying assisted reproductive technologies such as IVF and related procedures., • Maintain up-to-date knowledge of advances in transgenic and assisted reproductive technologies and relevant scientific literature, and apply this knowledge to develop or improve technologies and workflows., • Independently execute complex experimental designs and processes, ensuring high-quality, reproducible results., • Begin to design routine experiments and processes under general guidance, incorporating best practices and scientific rigor., • Consistently follow, critically evaluate, and refine appropriate methods, protocols, and standard operating procedures., • Apply independent judgment, with input from colleagues, to make sound scientific and operational decisions of limited to moderate complexity., • Engage in active questioning and discussion to fully understand the context, objectives, and interpretation of assigned work., • Make detailed observations during experiments, record data accurately, analyze results quantitatively and qualitatively, and interpret findings in a scientifically sound manner., • Prepare clear and comprehensive technical reports, summaries, protocols, and quantitative analyses as required by projects and stakeholders., • Collaborate with project teams on the design, execution, and interpretation of experiments and projects related to genetically engineered animal models and assisted reproductive technologies., • Attend internal meetings to represent the embryology group, present data updates, and contribute scientific insights when needed., • Work closely with colleagues in the technology center to drive innovative genetic engineering approaches for generating genetically engineered animal models., • Advance assisted reproductive technologies to facilitate efficient study cohort generation and support ongoing research programs., • Contribute to a collaborative, problem-solving culture by interacting effectively with team members and demonstrating enthusiasm for tackling challenging scientific problems. Essential Skills • Bachelor’s or Master’s degree (0–3+ years of experience) in biology, embryology, or a related field with proven laboratory experience., • Strong in the practical aspects of embryology, including handling and preparation of embryos and gametes., • Strong conceptual understanding of embryology, reproductive biology, and transgenic biology., • Experience working in a laboratory environment, including adherence to protocols, documentation, and safe laboratory practices., • Ability to independently execute complex experimental procedures and processes with high attention to detail., • Ability to follow and critically evaluate methods and protocols, and to identify opportunities for improvement., • Demonstrated skill in data collection, quantitative analysis, and interpretation of experimental results., • Effective collaboration skills, with the ability to interact productively with team members and project stakeholders., • Enthusiasm for tackling difficult scientific problems and contributing to innovative solutions., • Strong communication skills for preparing technical reports, summaries, and protocols, and for presenting data in internal meetings. Additional Skills & Qualifications • Assisted reproductive technologies, such as IVF and related reproductive procedures, is highly desirable., • Experience with gene editing technologies and their application to embryos or gametes is highly desirable., • Experience generating various genetically modified animal models is preferred., • Familiarity with transgenic biology techniques and technologies used to create genetically engineered models., • Ability to stay current with scientific literature in embryology, reproductive biology, transgenic biology, and gene editing., • Experience working within multidisciplinary research teams in a biotechnology or pharmaceutical setting is beneficial., • Strong motivation to contribute to drug discovery efforts through the development of innovative genetically engineered models., • Ability to represent a functional group in internal meetings and provide clear, concise data updates. Work Environment This is a three-month, Monday–Friday onsite position based in a laboratory environment within a technology center focused on genetically engineered models and assisted reproductive technologies. The role involves hands-on work with embryos, gametes, and genetically modified animal models, using laboratory equipment and gene editing tools in a controlled research setting. The broader organization offers an excellent company culture and is recognized as a top employer, with a strong track record of in-house invention and development of approved medicines and a growing global workforce. Onsite amenities may include a gym, cafeteria, and fully staffed daycare for eligible full-time employees. Full-time employee offerings can include stock options or equity, bonuses, restricted stock units, and 401(k) matching, while contract employees may receive accrued vacation and sick time, along with paid company-observed holidays. The environment emphasizes collaboration, scientific innovation, and support for professional growth within an expanding organization. Job Type & Location This is a Permanent position based out of Tarrytown, NY. Pay and Benefits The pay range for this position is $40.00 - $45.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Tarrytown,NY. Application Deadline This position is anticipated to close on Jun 19, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionJob Title: Associate Scientist – Embryology (Contract) Job Description This temporary Associate Scientist, Embryology role focuses on developing and applying innovative assisted reproductive and genetic engineering technologies to generate genetically engineered animal models that support drug discovery. The position prepares and manipulates embryos and gametes, introduces genetic modifications using appropriate methods, and supports cohort generation through advanced assisted reproductive technologies. The Associate Scientist works closely with a multidisciplinary project team, independently executes complex experimental procedures, and contributes to the design, execution, analysis, and interpretation of experiments while staying current with advances in embryology, reproductive biology, and transgenic technologies. Responsibilities • Prepare staged embryos or gametes for manipulation using established and emerging laboratory techniques., • Introduce genetic modifications into embryos or gametes using appropriate gene editing and related methods., • Transfer manipulated or in vitro fertilization (IVF)-derived embryos into recipient females to generate experimental cohorts., • Support cohort generation and preservation by applying assisted reproductive technologies such as IVF and related procedures., • Maintain up-to-date knowledge of advances in transgenic and assisted reproductive technologies and relevant scientific literature, and apply this knowledge to develop or improve technologies and workflows., • Independently execute complex experimental designs and processes, ensuring high-quality, reproducible results., • Begin to design routine experiments and processes under general guidance, incorporating best practices and scientific rigor., • Consistently follow, critically evaluate, and refine appropriate methods, protocols, and standard operating procedures., • Apply independent judgment, with input from colleagues, to make sound scientific and operational decisions of limited to moderate complexity., • Engage in active questioning and discussion to fully understand the context, objectives, and interpretation of assigned work., • Make detailed observations during experiments, record data accurately, analyze results quantitatively and qualitatively, and interpret findings in a scientifically sound manner., • Prepare clear and comprehensive technical reports, summaries, protocols, and quantitative analyses as required by projects and stakeholders., • Collaborate with project teams on the design, execution, and interpretation of experiments and projects related to genetically engineered animal models and assisted reproductive technologies., • Attend internal meetings to represent the embryology group, present data updates, and contribute scientific insights when needed., • Work closely with colleagues in the technology center to drive innovative genetic engineering approaches for generating genetically engineered animal models., • Advance assisted reproductive technologies to facilitate efficient study cohort generation and support ongoing research programs., • Contribute to a collaborative, problem-solving culture by interacting effectively with team members and demonstrating enthusiasm for tackling challenging scientific problems.Essential Skills, • Bachelor’s or Master’s degree (0–3+ years of experience) in biology, embryology, or a related field with proven laboratory experience., • Strong background in the practical aspects of embryology, including handling and preparation of embryos and gametes., • Strong conceptual understanding of embryology, reproductive biology, and transgenic biology., • Experience working in a laboratory environment, including adherence to protocols, documentation, and safe laboratory practices., • Ability to independently execute complex experimental procedures and processes with high attention to detail., • Ability to follow and critically evaluate methods and protocols, and to identify opportunities for improvement., • Demonstrated skill in data collection, quantitative analysis, and interpretation of experimental results., • Effective collaboration skills, with the ability to interact productively with team members and project stakeholders., • Enthusiasm for tackling difficult scientific problems and contributing to innovative solutions., • Strong communication skills for preparing technical reports, summaries, and protocols, and for presenting data in internal meetings.Additional Skills & Qualifications, • background in assisted reproductive technologies, such as IVF and related reproductive procedures, is highly desirable., • Experience with gene editing technologies and their application to embryos or gametes is highly desirable., • Experience generating various genetically modified animal models is preferred., • Familiarity with transgenic biology techniques and technologies used to create genetically engineered models., • Ability to stay current with scientific literature in embryology, reproductive biology, transgenic biology, and gene editing., • Experience working within multidisciplinary research teams in a biotechnology or pharmaceutical setting is beneficial., • Strong motivation to contribute to drug discovery efforts through the development of innovative genetically engineered models., • Ability to represent a functional group in internal meetings and provide clear, concise data updates.Work Environment This is a three-month, Monday–Friday onsite position based in a laboratory environment within a technology center focused on genetically engineered models and assisted reproductive technologies. The role involves hands-on work with embryos, gametes, and genetically modified animal models, using laboratory equipment and gene editing tools in a controlled research setting. The broader organization offers an excellent company culture and is recognized as a top employer, with a strong track record of in-house invention and development of approved medicines and a growing global workforce. Onsite amenities may include a gym, cafeteria, and fully staffed daycare for eligible full-time employees. Full-time employee offerings can include stock options or equity, bonuses, restricted stock units, and 401(k) matching, while contract employees may receive accrued vacation and sick time, along with paid company-observed holidays. The environment emphasizes collaboration, scientific innovation, and support for professional growth within an expanding organization. Job Type & Location This is a Contract position based out of Tarrytown, NY. Pay and Benefits The pay range for this position is $40.00 - $45.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Tarrytown,NY. Application Deadline This position is anticipated to close on Jun 16, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Melissa Owens| President P: (386)339-0839 |E: melissa@alliedsearchpartners.com Schedule a Meeting: https://calendly.com/melissaowens Allied Search Partners Allied Search Partners is back by two decades of healthcare staffing excellence. We are a trusted healthcare staffing firm supporting medical and dental offices nationwide. We partner with private practices and corporate healthcare organizations to provide reliable, well-supported temporary professionals—while prioritizing fair pay, consistency, and respect for our workers’ time. Our team offers 24/7 scheduling support and access to shifts through our efficient temp scheduling application. Unlike traditional staffing agencies that push one-off shifts to large candidate pools, we focus on long-term relationships with both our healthcare facilities and our workers. Job Description Job ID: 3563563 Job Title: Clinical Laboratory Scientist - Microbiologist Location: South Westchester County, NY Shift: Clinical Laboratory Scientist • Per Diem: Every other weekend, 8am-4pm Clinical Laboratory Scientist-Microbiology • Full Time: Monday to Friday. 8am - 4pm, Alternate Weekends & Holidays Job Summary: The Clinical Laboratory Scientist performs laboratory testing using both manual and automated techniques. Performs Bacteriology, Parasitology, Virology, Mycology, Mycobacteriology, Susceptibilities, and Molecular testing and other duties as assigned. Job Responsibilities: • Understands and adheres to the performance standards, policies, and behaviors, • Laboratory testing personnel responsibilities include:, • Following the laboratory’s pre-analytic and analytic procedures and maintaining records of these tests, • Maintaining records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens, • Adhering to the laboratory’s quality assurance procedures, including documenting all:, • Quality control activities including quality control testing and calibrations, • Instrument and equipment verifications, • Maintenance and preventative maintenance, • Following the laboratory’s policies and procedures whenever test systems are not within the laboratory’s established performance specifications, • Identifying and documenting problems that may adversely affect test performance and notifying the supervisor, assistant director or director and documenting all corrective actions taken when test systems deviate from the laboratory’s established performance specifications, • Ensures the accuracy and quality of all results from pre-analytic, analytic, and post-analytic phases of testing., • Notifies and documents clinicians and patient units of all critical values and maintains the laboratory STAT turn around time requirements., • Participates in regulatory readiness for CAP, AABB, NYSDOH, and Joint Commission., • Maintains 12 Continuing Education credits per year., • Understands and participates in standard operating procedures, proficiency testing, inspection audits, quality program including reporting non-conformances., • Evaluates test results for abnormalities and confirms those results per department protocols where required., • Participates in validations, training, and competency assessments as required., • Responsible for inventory management of lot numbers, expiration dates, labeling, and QC requirement., • Completes all annual mandatory training, in-services, and ongoing education as required., • Performs other duties as assigned., • Section testing training and competency assessments are maintained by the section laboratory supervisor for all assigned disciplines Qualifications: • Current NYS License as a Clinical Laboratory Technologist required., • Education in accordance with the NYS Office of Professions and CLIA requirements of testing personnel., • Preferred with ASCP Certification. Core Competencies: • Flexibility, • Organized, • Adaptability, • Attention to Detail, • Stress Tolerance Work Environment: May be exposed to chemicals necessary to perform required tasks. Any hazardous chemicals the employee may be exposed to are listed in the hospital’s SDS (Safety Data Sheet) data base and may be accessed through the hospital’s Intranet site (Employee Tools/SDS Access). A copy of the SDS data base can also be found at the hospital switchboard, saved on a disc. Note: The responsibilities and tasks outlined in this job description are not exhaustive and may change as determined by the needs hospital.

Job Description Clinical Laboratory Scientist, Histotechnologist, or Histotechnician White Plains, New York Full-Time | Evening Shift | Monday–Friday A leading hospital laboratory is seeking a detail-oriented Clinical Laboratory Scientist or Histotechnician to join its Anatomic Pathology team. This role is open to candidates from either a Clinical Laboratory Science or Histology background with the appropriate New York State licensure and experience. This role is responsible for performing histological procedures and laboratory testing using both manual and automated techniques to produce high-quality pathology slides and accurate laboratory results that support patient diagnosis and care. This is an excellent opportunity for a licensed laboratory professional who thrives in a fast-paced clinical environment and is committed to quality, precision, and patient safety. Schedule • Full-Time, • Evening Shift, • Monday – Friday, • 2:00 PM – 10:00 PM Compensation • Salary Range: $94,000 – $121,000 annually, • Histotechnologist - $94,000 – $121,000 (based on full-time employment), • Histotechnician - $64,000 - $95,000 (based on full-time employment) Compensation is based on experience, education, certifications, and internal equity. Position Responsibilities Clinical Laboratory Scientist Responsibilities • Perform laboratory testing in accordance with established laboratory procedures and quality standards, • Ensure accuracy throughout pre-analytic, analytic, and post-analytic testing phases, • Maintain quality control, calibration, maintenance, and proficiency testing records, • Identify and troubleshoot testing issues and document corrective actions, • Notify clinicians and patient care units of critical values while meeting STAT turnaround requirements, • Participate in CAP, AABB, NYSDOH, and Joint Commission regulatory readiness activities, • Assist with validations, competency assessments, inspections, and quality improvement initiatives, • Maintain inventory control, lot tracking, expiration monitoring, and quality assurance documentation, • Complete continuing education requirements and mandatory training programs Histotechnologist / Histotechnician Responsibilities • Perform embedding and sectioning of tissue blocks according to established protocols, • Evaluate routine H&E stains and correct inconsistencies prior to slide release, • Perform and evaluate special stains and immunohistochemistry procedures, • Review and document positive and negative controls for all staining procedures, • Maintain adherence to quality standards, sterile practices, and laboratory policies, • Support pathology operations and workflow efficiency Qualifications Clinical Laboratory Scientist Requirements • Current New York State License as a Clinical Laboratory Technologist, Histotechnologist, or Physician Assistant required, • Education meeting NYS Office of Professions and CLIA requirements, • ASCP Certification preferred Histotechnologist / Histotechnician Requirements • Current New York State Clinical Laboratory Technician License or Histotechnician License required, • Degree in Medical Technology or related science preferred, • One year of hospital histology experience preferred, • ASCP Certification preferred Core Competencies • Strong attention to detail and accuracy, • Excellent organizational and multitasking skills, • Adaptability and flexibility, • Strong stress tolerance and focus, • Ability to work independently and collaboratively

The clinical laboratory technologist position entails following the established and approved protocols of the department of health, performs clinical laboratory procedures and examinations and any other tests or procedures conducted by a clinical laboratory, including maintaining equipment and recor

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