Clinical Laboratory Technologist IV (2nd Shift - Mon, Thurs, Fri, Sat 1:30 PM - 12:00 AM EST) #4204

• Perform tasks which require the exercise of independent judgment and responsibility, with minimal supervision by the director or supervisor. 
• Perform pre-analytical and analytical procedures including testing, quality control, preparation and aliquoting of reagents, analyses, and maintain records of tests according to the laboratory’s standard operating procedures. 
• Maintaining records that demonstrate proficiency testing samples are tested in the same manner as patient specimens. 
• Adhere to laboratory’s quality assurance procedures, including documenting all: Quality control activities, Instrument and equipment verifications 
• Maintenance and preventive maintenance 
• Follow the laboratory’s policies and procedures whenever test systems are not within the laboratory’s established performance specifications. 
• Identify and document problems that may adversely affect test performance and notifying the supervisor, assistant director, or director. 
• Document all corrective actions taken when test systems deviate from the laboratory’s established 
• performance specifications. 
• Operate and maintain laboratory instruments and equipment according to laboratory standard operating procedures. 
• Troubleshoot and problem solve instrument issues. 
• Check and record temperature and perform root cause analysis of deviations and initiate a service request as necessary.
• Review, and interpret patient data as assigned. 
• Perform and document reagent qualifications per the approved protocols.
• Perform and document routine preventive maintenance. 
• Perform, review and document laboratory quality control procedures. 
• Report all concerns of test quality and/or safety to the Laboratory Manager or Safety Officer. 
• Communicate effectively with coworkers and non-laboratory personnel. 
• Identify process improvement opportunities and report to laboratory management. 
• Provide updates to Laboratory Supervisors/Leads regarding any issues. 
• Monitor data and process status as needed. 
• Participate in daily, weekly and monthly laboratory cleanliness activities/procedures. 
• Independently identify and troubleshoot minor problems that adversely affect the test performance. 
• Assist in sample and process troubleshooting. 
• Assist with training of new laboratory personnel and training of new procedures with existing personnel. 
• Participate in introduction of assay improvements, new assay configurations and validation. 
• Participate in cross-functional teams responsible for securing CLIA certification, CAP accreditation, and state licensure for the GRAIL Clinical Laboratory, including compliance with all applicable standards and regulations. 
• Perform other laboratory duties as needed.

Preferred Qualifications

• Bachelor’s degree in medical technology or laboratory science from an accredited institution OR
• Bachelor’s degree in one of the chemical, physical, or biological sciences from an accredited institution and at least 6 months of acceptable supervised experience and/or relevant training.
• 2 years of Clinical lab experience 
• Experience in molecular biology techniques preferred 
• Working knowledge of local, state and federal laboratory regulations preferred 
• Able to integrate and apply feedback in a professional manner 
• Able to prioritize and drive to results with a high emphasis on quality 
• Ability to work as part of a team within a highly collaborative environment 
• Strong computer skills 
• Ability to analyze and solve basic issues that impact the performance of the assay 
• Ability to proactively communicate consistently, clearly and honestly 
• Ability to prioritize tasks with a high emphasis on quality 
• Ability to participate in projects and complete assignments as expected 
• Flexibility of work schedule to meet the needs of GRAIL’s Clinical Laboratory