General Supervisor Complexity CLIA LAB
Job in
Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for:
Nanobiosym
Full Time
position
Listed on 2026-01-15
Job specializations:
-
Healthcare
Clinical Research, Medical Technologist & Lab Technician
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly
USD
60000.00
80000.00
YEAR
Job Description & How to Apply Below
Position: General Supervisor for High Complexity CLIA LAB
Nanobiosym is an innovative company in Cambridge, MA that is developing novel technologies to address a broad range of diseases. Nanobiosym was founded by an MIT/Harvard alum to work at the interface of physics, nanotechnology, and biomedicine. This hypergrowth company allows for unique career opportunities with strong long‑term incentives. Nanobiosym is currently seeking top‑notch candidates to help the company scale up its operations.
Nanobiosym is looking for a General Supervisor for its High‑Complexity Testing CLIA LAB. The role and requirements are below. The purpose of the Laboratory General Supervisor is to serve as a general supervisor under CLIA 42 CFR 493.1449 regulations for a molecular diagnostics lab. You will assist the Clinical Laboratory Director in day‑to‑day personnel, workflow, quality control, and equipment management. You are responsible for ensuring that the tests meet all regulatory requirements and coordinating with the laboratory staff to review data for accuracy and issue test reports in a timely manner.
Job Responsibilities:Provide leadership and directs a team of technologists through positive communication and supportTrain new personnel with regard to technical and operational proceduresEnsure all laboratory members are proficient in assay processing including biannual (first year and subsequent annual competency training)Organize specimens required to be runReview data for concordant analysis, write‑up results, and file data with the assay tested under competency runsAnnually evaluate and document the performance of all testing personnelCreate daily/weekly technologist schedule for molecular diagnostic assaysSetting‑up equipment and resources for the laboratoryMonitor examinations to ensure that acceptable levels of analytic performance are maintained and meet TATsEnsure that all remedial actions are taken whenever test systems deviate from the laboratory's established performance specificationReport quality issues directly to the Clinical Laboratory DirectorTrack proficiency testing for the validated assay in the laboratory that includes calendar tracking, and following through concordance analysis and finalizing all documents in the database for any future inspectionsMaintain all Quality Management System on instrument maintenance programs, i.e. preventative maintenance, cleanliness and maintain records of service in compliance CAPMaintain and manage daily performance and workload distributed throughout the laboratoryReview issues regarding problem cases with Clinical Laboratory Director to get direction for troubleshooting and next step directionsWork with the lab team to monitor and maintain inventory of supplies, place orders of materialsParticipate with Clinical Laboratory Director in managing all governmental and regulatory auditsManage and monitor Quality Control (QC), Quality Assurance (QA), Safety and Inspection practices to assure compliance with CLIA and MA regulationsDevelop, implement and maintain SOPs as per CLIA and MA regulationMaintain a flexible schedule to meet laboratory goalsQualifications:Qualified as a Director for high‑complexity testing;OR Qualified as a Technical Supervisor for high complexity testing;OR Doctoral degree in clinical laboratory science or chemical, physical or biological science with 1 year training and experience in high‑complexity testing;OR Master's degree in clinical laboratory science, medical technology or chemical, physical or biological science and 1 year training and experience in high‑complexity testing;OR Bachelor's degree in clinical laboratory science, medical technology or chemical, physical or biological science and 1 year training and experience in high‑complexity testing;OR Associate degree in medical laboratory technology (or pulmonary function) and 2 years laboratory (or blood gas analysis) training or experience, or both, in high complexity testing Refer to the CLIA regulation 42
CFR
493.1461 for additional qualifications#J-18808-Ljbffr
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