Medical Laboratory Technologist

TridentCare • Middletown, CT

14h • $27 - $32 • Onsite

About The Position

This is a full-time, 2nd shift position (2:00 PM - 10:30 PM, Monday-Friday with rotating weekends) for a Medical Laboratory Technologist. The role involves performing various laboratory tests, ensuring quality control, data entry, specimen processing, and assisting with instrument maintenance and inventory. The position also includes compliance responsibilities and requires strong communication, organizational, and computer skills.

Requirements

• Must have either a Bachelor’s Degree and MT (ASCP), or an Associated Degree with MLT certification or equivalent degree in health science.
• Must have a concept with all phases of the operation of the automated instruments utilized for routine analysis.
• Candidates must have sound computer skills.
• Must qualify under CLIA as a Medical Technologist or Medical Laboratory Technician

Nice To Haves

• One year experience in chemistry/hematology preferred but not required.
• Good planning and organizational skills desirable.

Responsibilities

• Plates Microbiology samples
• Performs testing in the areas of Chemistry, Hematology, Urinalysis and Coagulation.
• Checks the quality control of each test prior to running and reporting patient results.
• Calls worklists on the computer, does editing of results and data enters test results.
• Confirms abnormal results prior to releasing and bring any “rare and improbable” test results to the attention of a supervisor.
• Processes specimens and logs requisitions as needed.
• Reviews daily specimen management reports.
• Assists the Laboratory Supervisor in training new employees.
• Troubleshoots problems (client, instrument, computer) as needed.
• Performs maintenance on the automated Chemistry, Hematology, Coagulation and Urinalysis instrumentation as needed.
• Assists in maintaining an adequate inventory of supplies. Records lot numbers and compliance with state requirements for documentation of lot numbers with quality control and specimen records.
• Records the quality control and maintains the QC records on all assays performed.
• Data enters results into the computer.
• Ensures that QC is within appropriate limits and brings problems to supervisor.
• Reviews worklists and work from automated analyzers to ensure accuracy and timely reporting of patient results.
• Performs differentials and urine sediments as needed.
• Performs other tasks and procedures that are commensurate with education, training and abilities.
• Responsible for all clerical functions associated with specimen integrity, testing, identification and reporting of department testing.
• Follows all safety protocols as outlined in safety manual.
• Identifies and pursues self-improvement needs
• Seeks coaching/mentoring when appropriate
• Performs other duties as assigned.
• Complies with applicable legal requirements, standards, and procedures including, but not limited to, those within the Compliance Process, Code of Conduct, and Corporate Integrity Agreement (CIA).
• Participates in required orientation, Compliance and HIPAA training programs.
• Reports concerns and suspected incidences of non-compliance using the 4-Step Reporting Process
• Cooperates with monitoring and audit functions and investigations.
• Participates, as requested, in process improvement responsibilities.

Benefits

• Two weeks of vacation time
• Health Insurance after 30 days!
• Sick time
• 8 paid holidays
• Medical insurance allowance, giving you the freedom to customize your plan to fit your needs
• Dental insurance
• Vision insurance
• Disability insurance
• Company paid life insurance.
• 401(k)

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree