Qualified as a Director or Technical Supervisor for high-complexity testing
Doctoral degree in a relevant scientific field with 1-year experience in high-complexity testing
Master's degree in a relevant scientific field with 1-year experience in high-complexity testing
Bachelor's degree in a relevant scientific field with 1-year experience in high-complexity testing
Associate degree in medical laboratory technology with 2 years of high-complexity testing experience
Responsibilities
Lead and support a team of technologists
Train new personnel on technical and operational procedures
Ensure proficiency in assay processing for all laboratory members
Organize and manage specimen workflow
Review and document laboratory test results and data accuracy
Evaluate and document the performance of laboratory personnel annually
Create and manage technologist scheduling for molecular diagnostic assays
Set up laboratory equipment and resources
Monitor analytical performance and turnaround times to ensure quality
Report quality issues to the Clinical Laboratory Director
Track proficiency testing and maintain compliance records
Manage quality control and assurance practices as per regulations
Develop and maintain standard operating procedures according to regulatory standards
Monitor inventory and place orders for laboratory supplies
Participate in regulatory audits with the Clinical Laboratory Director
Benefits
Unique opportunities for career growth in a hypergrowth company
Strong long-term incentives for employees
Innovative work at the intersection of physics, nanotechnology, and biomedicine
Collaborative and supportive work environment
Potential to impact a broad range of diseases through advanced technologies
Full Job Description
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 [redacted] 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 tests reports in a timely manner.
Job Responsibilities:
Provide leadership and directs a team of technologists through positive communication and support
Train new personnel with regard to technical and operational procedures
Ensure all laboratory members are proficient in assay processing including biannual (first year and subsequent annual competency training)
Organize specimens required to be run
Review data for concordant analysis, write-up results, and file data with the assay tested under competency runs
Annually evaluate and document the performance of all testing personnel
Create daily/weekly technologist schedule for molecular diagnostic assays
Setting-up equipment and resources for the laboratory
Monitor examinations to ensure that acceptable levels of analytic performance are maintained and meet TATs
Ensure that all remedial actions are taken whenever test systems deviate from the laboratory's established performance specification
Report quality issues directly to the Clinical Laboratory Director
Track 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 inspections
Maintain all Quality Management System on instrument maintenance programs, i.e. preventative maintenance, cleanliness and maintains records of service in compliance CAP
Maintain and manage daily performance and workload distributed throughout the laboratory
Review issues regarding problem cases with Clinical Laboratory Director to get direction for troubleshooting and next step directions
Work with the lab team to monitor and maintain inventory of supplies, place orders of materials
Participate with Clinical Laboratory Director in managing all governmental and regulatory audits
Mange and monitor Quality Control (QC), Quality Assurance (QA), Safety and Inspection practices to assure compliance with CLIA and MA regulations
Develop, implement and maintain SOPs as per CLIA and MA regulation
Maintain a flexible schedule to meet laboratory goals
Qualifications:
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 42CFR[redacted] for additional qualifications
