Medical Technologist

Medical Laboratory Scientist, Senior IStarting Rate: $35.01/hourNight shift- Ask about the differential!Free ParkingExcellent benefits as of day oneWe're offering a $10,000 sign-on bonus to welcome you to our team.SummaryAs required by CLIA, the testing personnel are responsible for specimen processing, test performance, and reporting test results. Each individual performs only those tests that are authorized by the laboratory director and require a degree of skill commensurate with the individual's education, training, or experience, and technical abilities. Works independently in an efficient and organized manner to assure accurate results and records. The work requires a professional level of knowledge to read and interpret accurately test results used by providers in the diagnosis and treatment of diseases. The Medical Laboratory Scientist, Senior I, in their role as Technical Supervisor, Technical Consultant, or General Supervisor as defined by CLIA, may be delegated the responsibility of the technical oversight of the laboratory, including the day-to-day supervision or oversight of the laboratory operation and personnel performing testing and reporting results. Under the general supervision of the Technical Director and Clinical Supervisors, the Senior Technologist I is responsible for supervision of assigned workstations, including Quality Control (QC) review, training, competency assessment of staff, and inventory management.Essential FunctionsAfter success completion of orientation, training and competency assessment on all instruments/methods applicable to their role:Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting, and maintaining records of patient test results.Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient samples.Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations, and maintenance performed.Follow the laboratory's established corrective action policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance.Be capable of identifying problems that may adversely affect test performance or reporting of test results, and either must correct the problems or immediately notify the general supervisor, technical consultant, technical supervisor, clinical consultant, or director; andDocument all corrective actions taken when test systems deviate from the laboratory's established performance specifications.QualificationsEducationBachelor's Degree Clinical Laboratory Sciences required or Bachelor's Degree Medical Technology required or Bachelor's Degree Laboratory Sciences requiredCan this role accept experience in lieu of a degree?NoLicenses and CredentialsMedical Technologist (ASCP) [MLT, MT, MLA, Histologists] - American Society for Clinical Pathology Board of Certification (ASCP-BOC) requiredExperienceLab experience 3-5 years requiredKnowledge, Skills and AbilitiesThe knowledge, both practical and theoretical, of tests and procedures necessary to review findings and advise and direct subordinates in action.Demonstrates advanced level of analytical skills and judgement.Must have understanding of computer technology and its application to analytical procedures and quality control.Must have a comprehensive understanding of laboratory equipment and its operation, maintenance, and repair, and analytic techniques.Must have the ability to work independently, evaluate situations and act appropriately.Ability to multitask in a fast-paced environment.Must have the ability to pay careful attention to detail and to adhere to written protocols, including communication with supervisors when issues are identified.Must be able to perform as a team member.Excellent interpersonal skills.Ability to interact professionally and effectively with numerous staff including physicians, hospital personnel, employees, and patients.Advanced knowledge of federal, state and accreditation requirements.