About the Job
The Immunohistochemistry (IHC) Technologist II performs routine Immunohistochemistry (IHC) testing on patient samples in a high complex clinical diagnostic laboratory using a variety of automated platforms for microscopic examination and analysis by a Pathologist.
Key Responsibilities
Performs Automated Immunohistochemistry (IHC) using both the Dako Autostainer Link 48 and Ventana Benchmark Ultra Staining Systems. Operates a microtome to produce slides or curls from paraffin blocks. Monitors oven timers to unload slides, places them on flats and distributes them to the appropriate staining platform areas. Handles, prepares, and unloads stainers; conducts dehydrating and cover-slipping of slides utilizing manual or automatic systems (Leica stainer). Prepares bulk fluids for stainers and refills as needed, keeping track of lot numbers and associating bulks to instruments after filling them. Performs the assigned tests or components of the test in accordance with assay run schedule, accurately, and within TAT and always in compliance with written SOPs. Performs QC and/or verification steps for receiving and delivering specimens for IHC staining. Finalizes test orders to deliver to requesting pathologist. Performs QC testing on control tissues and reagents. Performs routine H&E staining with possible other histological staining methods introduced over time. Maintains attention to detail for quality completion of each task. Sorts and labels samples by test requested while maintaining sample integrity. Maintains proper sample chain of custody including proper specimen handling, labeling and preparation of batch records. Maintains adequate stock and efficient use of supplies necessary for performing all procedures, and preparation of reagents as required. Performs routine scanning of stained slides with the Aperio ScanScope. Ability to utilize a laboratory information management system (LIMs, MS Office esp. Excel). Follows written lab Standard Operating procedures for the correct handling and processing of specimens. Assists in maintaining and troubleshooting equipment/instrumentation. Effectively communicates deficiencies to appropriate personnel, including deficiencies related to specimens, paperwork, database information, and equipment. Ability to investigate Root Cause Analysis (RCA), write Incident/Event Report (INC), and Non-Conformance Report (NCR) under senior Technologist guidance. Complete projects under guidance of senior lab personnel. Adhere to laboratory’s quality control policies (GCP, CAP/CLIA, ISO) and document all quality control activities with the ability to recognize outliers and correct them. Participate in biohazard, chemical, and general safety and other continuing education programs. Receives and transmits telephone calls and/or emails regarding patient sample processing. Resolve high volume email inquiry request. Communicate effectively in a courteous, professional manner with all levels of management, co-workers, and clients to provide quality customer service. Work effectively within a team-oriented department and company. As needed, flexes to cover scheduling gaps and is included in the on-call rotation for additional weekend and/or holiday technical support. Perform other duties as assigned.Qualifications:
Basic Qualifications:
Bachelor’s degree, particularly a Bachelor of Science degree in biological or life sciences 2+ years of Histology/IHC work experience in a CAP/CLIA regulated laboratory 2+ years of experience working with Dako, Leica, or Ventana platforms, or manual methods 2+ years of microtomy experiencePreferred Qualifications:
Bachelor’s degree, particularly a Bachelor of Science degree in biological or life sciences 3+ years of laboratory work experience in a CAP/CLIA regulated lab 3+ years of experience in Histology experience 3+ years of experience in Immunohistochemistry testing (manual and automated) Certified Histotechnician (HT) or Histotechnologist (HTL) or Qualification in Immunohistochemistry (QIHC) by American Society for Clinical Pathology (ASCP) Demonstrated attention to detail and strong organizational skills Familiarity with Laboratory Information Management Systems (LIMS) Relevant experience in a regulated laboratory environment (such as CAP/CLIA) Demonstrated ability to: Learn new tasks in appropriate timeframes Prioritize and thoroughly follow up on assigned tasks Understand and communicate scientific or technical information Basic knowledge of laboratory safety protocols Understanding of HIPAA and the importance of privacy of patient data Demonstrated experience working within tight timelines for successful execution of project and program goals Demonstrated experience handling multiple tasks at once Ability to work independently as well as collaborate with peers in a fast-paced and cross-functional results-oriented team environment Ability to work well under pressure while maintaining a professional demeanor Ability to prioritize and thoroughly follow up on assigned tasks Ability to adapt to changing procedures, policies and work environment Ability to perform work in a lab environment in the presence of chemicals and reagents Strong interpersonal skills that include excellent skills in written and oral communication, collaboration, and problem solving Understanding of HIPAA and importance of privacy of patient data Commitment to FMI values: Integrity, Courage, PassionThe expected salary range for this position based on the primary location of Morris is $55,000 – $63,500 per year. The salary range is commensurate with Foundation Medicine’s compensation practice and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for Foundation Medicine's benefits.
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