The Medical Laboratory Scientist II (MLS II), in their role as Testing Personnel as defined by CLIA, may perform waived and non-waived testing. 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. Under general supervision, and after successful completion of orientation, training, and competency assessment on all instruments/methods applicable to their role, the Medical Laboratory Scientist II (MLS II) carries out all policies and performs all tests in accordance with the laboratory's standard operating procedures. 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 II (MLS II), in their role as General Supervisor as defined by CLIA, on occasion, may be delegated the responsibility of the day-to-day supervision or oversight of the laboratory operations and personnel performing testing and reporting results, if the number of years' experience, required by regulatory agencies, is met. Under the general supervision of the Clinical Manager and Clinical Supervisors, the Medical Laboratory Scientist II (MLS II) may assist with assigned workstations including Quality Control (QC) review, instrument maintenance and troubleshooting, training, competency assessment of staff, operations, and inventory management. Reports to: Clinical Manager and Clinical Supervisor.


Responsibilities as outlined by CLIA: General Supervisor - High Complexity Testing On occasion, may be assigned the following responsibilities, if the number of years' experience, required by regulatory agencies, is met. 1. Must be accessible to test personnel at all times testing is performed and provide on-site telephone or electronic consultation to resolve technical problems in accordance with policies and procedures established in the clinical laboratory. 2. Is responsible for providing day-to-day supervision of high-complexity test performance by qualified testing personnel and 3. Must be on-site to provide direct supervision when high complexity testing is performed by an individual qualified before 1/19/1993 (FR 493/1489(b)(5). Referred to Federal Register for exceptions when work can be reviewed within 24 hours by a general supervisor qualified under Fr 493.1461. and 4. Is responsible for monitoring test analyses and specimen examinations to ensure that acceptable levels of analytical performance are maintained. Testing Personnel are responsible for specimen processing, test performance and for reporting test results. 5. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results; 6. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens; 7. Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed; 8. Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance; 9. 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 supervisor, clinical consultant, or director; 10. Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications; and 11. If qualified under §493.1489(b)(5), perform high complexity testing only under the onsite, direct supervision of a general supervisor qualified under §493.1461.


Additional responsibilities may include the following under the direction of the Clinical Manager and Clinical Supervisor: 1. Performs qualitative and quantitative tests and procedures using instruments and/or manual methods on blood, plasma, and other body fluids, according to laboratory policies. Demonstrates the use of two patient identifiers. 2. Prepares samples and reagents for testing according to laboratory policies. 3. Operates all instruments/analyzers per established procedures or instructions in applicable operator's manual. 4. Performs routine maintenance, function checks or calibrations on equipment according to policies and documents. 5. Recognizes instrument malfunctions, documents problems as may be required, performs troubleshooting and repair according to established guidelines. Alerts supervisor or designee as needed. 6. Performs quality control for all reagents and instruments according to policies. Documents quality control results according to laboratory policies. Responsible to document all out of range QC results and corresponding corrective action steps if applicable. 7. Ensures the accuracy, interpretation, and reporting of test results according to laboratory policies. 8. Identifies aberrant patient test results, recognizes factors that affect results, and takes appropriate action; seeks assistance in resolution as needed. Documents all corrective action procedures undertaken in the clinical laboratory. 9. Participates in QA/QI activities as required. 10. Participates in Proficiency Testing program including the handling and analysis of Proficiency Testing samples. 11. Successfully completes orientation, training, and competency for all applicable instruments/methods. Maintains competency. 12. Keeps current in developments in technical instrumentation and analytical techniques in clinical laboratory. Participates in internal and external continuing education. Completes mandatory annual training modules. 13. Participates in training/orientation of new employees or students. Participates in the competency assessment of other staff as required. 14. Participates in the evaluation, validation and/or implementation of new methodologies or instruments as required. 15. May assist leadership with planning, organizing, and prioritizing work duties to accomplish daily tasks and objectives. Supports and assists coworkers as needed to ensure the best possible patient care; able to work independently while functioning as a team member. 16. May provide daily supervision and assistance to technical and non-technical staff. May determine work priority, assumes timely completion of work. Assumes weekend and holiday supervisory responsibilities in the absence of a supervisor. 17. May review daily work of others including patient results, quality control and maintenance records for accuracy and completeness. 18. Documents errors using hospital Safety Reporting System; informs supervisor/manager when safety reports are entered. 19. Adheres to hospital and laboratory policies and procedures including but not limited to laboratory procedures, hospital procedures, accrediting agencies' guidelines, infection control and safety plans. 20. Performs clerical and support services as needed, such as answering the telephone, calling Critical, Stat or Code results to the appropriate department or Licensed Care Provider, monitoring pending logs, and other assigned duties. Ensures that there is proper documentation of calls. 21. Monitors reagent and supplies, orders as needed, or communicates need to the appropriate person to maintain adequate inventory of necessary supplies. 22. Performs any other duties as required, which may include but not limited to general laboratory duties such as processing specimens, logging in specimens,



Qualifications

Education Degree Field of Study Required/Preferred: Bachelor's Degree 1. Minimum: Must possess a Bachelor of Science Degree in Medical Laboratory Science or Chemical, Physical, or biological science from an accredited college or university OR required or 2. Other qualifications as described in the Federal Register, 42 CFR, Subpart M 493.1403 - 1495. Can this role accept experience in lieu of a degree? Refer to Federal Register, 42 CFR, Subpart M 493.1403 - 1495.
Licenses and Certifications Licenses/Certifications: ASCP certification or equivalent (e.g., AMT) Required.


Relevant. Work Experience Details: Years of Experience Required/ Preferred: Clinical Laboratory experience >= 2 years - BS in MLS >= 3 years- BS in non-MLS >=4 years.


Required Work Performance Details: Documented performance (via annual evaluation) that fully meets or exceeds standard expectations Knowledge, Skills and Abilities The comprehensive knowledge, both practical and theoretical, of tests and procedures necessary to review findings and advise and direct subordinates in action. The manual/visual dexterity and skills necessary to operate adjust and make repairs to various types of automated and non-automated laboratory equipment. Must have a comprehensive understanding of laboratory equipment and its operation, maintenance and repair and analytic techniques. Can recognize problems with tests, QC, analyzers, and samples that could impact test results. Demonstrates ability to contribute to the review or development of new procedures. Demonstrates ability to identify and contribute to performance improvement, work re-design or quality/safety projects. Must have the ability to work independently, evaluate situations and act appropriately. Ability to multi-task in a fast-paced environment. Must have the ability to pay careful attention to detail and to adhere to written protocols. Must be able to perform as a team member, provide leadership, guidance, and direction to staff. The supervisory and managerial abilities necessary to direct and coordinate activities of personnel. Ability to oversee staff and make operational decisions. Excellent communication and interpersonal skills. Ability to interact professionally and effectively with numerous staff including physicians, hospital personnel, employees, and patients.



EEO Statement

Brigham and Women's Hospital is an Affirmative Action Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.