Medical Technologist 2, 2nd shift (2:00p -10:30pm)

University of Miami•Miami, FL

17h•Onsite

About The Position

The UHealth Laboratories Department at the University of Miami has an exciting opportunity for a Full Time Medical Technologist in the UTower Hospital. CORE JOB SUMMARY The Medical Technologist 2 (H) performs microbiological, molecular biological and immunological tests on body specimens to provide data for use in treatment and diagnosis of disease. Moreover, the incumbent facilitates quality assurance and instrument maintenance. CORE JOB FUNCTIONS Verifies identification of specimen with physicians’ orders, prepares specimens for testing, and handles all specimens in a safe and careful manner. Analyzes results of testing and interprets abnormal or unusual results. Researches and prepares all pertinent patient data and refers all data and testing results to pathologists for evaluation and sign-out. Calibrates equipment, orders supplies, and maintains inventory of relevant forms and materials. Recognizes test inconsistencies and takes appropriate corrective action while supporting laboratory co-workers in resolution of similar problems. Administers quality-control tests, according to procedure, and maintains appropriate data recording. Assists with orienting and training employees on laboratory techniques and operations. Adheres to University and unit-level policies and procedures and safeguards University assets. This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary. DEPARTMENT ADDENDUM Department Specific Functions 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 specimens. 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 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 supervisor, clinical consultant, or director. Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications. Document all regulatory logs, including but not limited to decontamination log, rejection log, Temperature and humidity log, and correcting report log. Participate in all laboratory compliance activities, including but not limited to Instruments or Method Validation, Linearities, inter/intra precision, Instruments to instruments comparison, QC troubleshooting/review, or any other performance study assigned. Participate in the training or competency of assigned new personnel or students, either undergrad or postgrad. Become competent in assigned core test systems during the initial period of training and become competent in the remaining test systems that the laboratory may need.

Requirements

Bachelor’s degree in relevant field
Current Florida Medical Technologist License
Minimum 2 years of relevant experience
Skill in completing assignments accurately and with attention to detail.
Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
Ability to process and handle confidential information with discretion.
Ability to work evenings, nights, and weekends as necessary.
Commitment to the University’s core values.
Ability to work independently and/or in a collaborative environment.
Demonstrates clear and effective verbal communication.
Exhibits proficient manual dexterity and fine motor skills for handling laboratory instruments and specimens.
Observes all laboratory safety protocols and maintains a clean, organized, and hazard-free work environment.
Demonstrates knowledge of hazardous chemical waste management, including: Proper identification and labeling of hazardous materials. Appropriate use of personal protective equipment (PPE). Understanding of hazardous waste characteristics, volume generation limits, and accumulation time limits. Implementation of spill control and prevention measures. Accurate recordkeeping and adherence to regulatory compliance. Safe handling, storage, and inspection of hazardous waste containers.
Maintains a safety-conscious and responsible attitude in all work practices.

Responsibilities

Verifies identification of specimen with physicians’ orders, prepares specimens for testing, and handles all specimens in a safe and careful manner.
Analyzes results of testing and interprets abnormal or unusual results.
Researches and prepares all pertinent patient data and refers all data and testing results to pathologists for evaluation and sign-out.
Calibrates equipment, orders supplies, and maintains inventory of relevant forms and materials.
Recognizes test inconsistencies and takes appropriate corrective action while supporting laboratory co-workers in resolution of similar problems.
Administers quality-control tests, according to procedure, and maintains appropriate data recording.
Assists with orienting and training employees on laboratory techniques and operations.
Adheres to University and unit-level policies and procedures and safeguards University assets.
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 specimens.
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 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 supervisor, clinical consultant, or director.
Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications.
Document all regulatory logs, including but not limited to decontamination log, rejection log, Temperature and humidity log, and correcting report log.
Participate in all laboratory compliance activities, including but not limited to Instruments or Method Validation, Linearities, inter/intra precision, Instruments to instruments comparison, QC troubleshooting/review, or any other performance study assigned.
Participate in the training or competency of assigned new personnel or students, either undergrad or postgrad.
Become competent in assigned core test systems during the initial period of training and become competent in the remaining test systems that the laboratory may need.