The Clinical Molecular Technologist is responsible for performing all aspects of testing in a molecular laboratory. The technologist will evaluate and introduce new materials, methods, and equipment to help determine the feasibility and/or adaptability of clinical molecular studies.

They assist the laboratory director in the development of new technologies and participate in documenting and implementing Quality Assurance (QA)/Quality Control (QC)/Quality Inventory (QI) procedures.

The Research and Development Scientist II (Molecular Diagnostics)  will perform method development and validations for new assays and periodic performance verification of the current assay. This individual will assist with the rollout of new methods and QA activities, write SOPs, implement laboratory safety plans, and train production staff regarding methods they have validated. They will assist with filling out all the paperwork associated with new LDTs submissions to NYS DOH CLEP.  

We are currently seeking a dynamic Specimen Accessioner who will support the laboratory technologists with sample intake. This entails following all relevant SOPs in receiving, opening, and logging newly received specimens for subsequent analysis

The director of QA oversees a QA team and works cooperatively with the lab technical, medical, and operation director(s), lab manager(s), and supervisors to integrate and maintain an efficient QMS, provide all needed training, and make the organization inspection ready at any moment.

Under the general supervision of the Pathologist in charge, the Histology Technician will prepare tissue specimens for microscopic examination and analysis. This role reports directly to the Director of Operations.