Clinical Laboratory Scientist Core Lab FT Nights

Clinical Laboratory Scientist Core Lab FT Nights Why a Great Place To Work You’re more than your job. Everyone is. And that’s what makes you great at your job—all the little extras you bring to work every day, the things that make you you. At LCMC Health we value those things about you, because we know that all those little extras add up to extraordinary. And we’ve built a culture that supports and celebrates the extraordinary. You’ll see it when you come to work here, in the spirit of our places and the faces of our people. And every patient we heal, every family we comfort, every life we improve is the outcome of countless little extras adding up to an extraordinary result. Join LCMC Health, and you’ll find that our everyday makes it easy to live your extraordinary. ThisEvaluate job description is intended to describe the general nature and level of work performed by employees assigned to this department. This is not an exhaustive list of all duties and responsibilities, and LCMC Health reserves the right to amend and change responsibilities to meet organizational needs as necessary. General Duties Ensures specimens received by the laboratory are acceptable for testing by applying the appropriate criteria. Changes or prepares reagents, controls as necessary and records such in log. Labels, accessions and distributes specimens so that integrity of patient identification is maintained throughout processing. Inoculates specimens from all areas of the body on appropriate media. Initiates orders for blood and/or blood components from the appropriate blood supplier. Follows hospital/laboratory safety and infection control policies and reports variances to section supervisors as they occur. Operates both primary and secondary instrumentation proficiently. Determines appropriateness of manual methods, micro-methods, back-up procedures and initiates such procedures. Through use of the computer system, compares patient results to previous results during the same encounter and investigates discrepancies. Reports test results within established departmental turn‑around times after verifying documentation is complete and accurate. Prepares and interprets gram stains and other wet and dry preparations for bacteriology and parasitology. Performs all routine procedures including, but not limited to, ABORH typing and retesting, antibody detection and identification, compatibility testing and serology procedures. Prepares blood components while maintaining aseptic technique and proper storage. Evaluates serological reactivity to assist with antibody identificationspent Nlogplicante and cross‑match incompatibilities. Follows universal precautions at all times when dealing with blood or body fluids. Disinfects counter tops at the end of the shift with appropriate cleaner. Operates, calibrates, conducts performance checks and maintains any clinical laboratory instrument or equipment after orientation. Troubleshoots basic instrument malfunctions and documents in the appropriate action log. Determines when an instrument’s service representative should be contacted for assistance. Analyzes quality control material for each procedure, records values according to section policy and reports to technical Supervisor when results are outside established limits. Performs comparison studies of precision, accuracy and linearity on new or existing procedures and reports results by established deadlines. Performs and accurately records proficiency surveys, properly routes form and copies within the specified time frame. Performs all aspects of reagent quality control as specified in the quality control manuals. Assists in the clinical orientation of new or less skilled laboratory personnel nua as requested by the section supervisor. Assures proper packaging and disposal of waste chemicals. Maintains proper documentation (log) of generated waste. Performs order or result entry (manual or computerized) and reviews information for accuracy before verification. Documents Critical Call Value notification, duplicate checking, date and time of performance, technologist initials and expected age‑related “normal” values on all down‑time reports as appropriate. Checks instruments and benches assigned for appropriate reagent and supply levels and replenishes when necessary. Notifies appropriate person of low inventory items or of any out‑of‑date reagents contaminated or otherwise unacceptable. Records receipt of supplies and reagents, properly initialing and dating the inventory items at receipt, time put into use and expiration. Ensures adequate inventory levels are available for incoming shifts. Receives Diário tissue specimens from surgery, autopsy and the nursing floors. Performs proper processing and preservation of tissue specimens. Complies with proper specimen storage and preservation of all other non‑tissue specimens for non‑core laboratory. Prepares necessary reagents and collection supplies for assisting with bone marrow aspirations according to physician orders. Assists physicians in the procurement of bone marrow specimens in accordance with departmental and Hospital policies. Performs special stains and follows protocols as appropriate. Minimum Qualifications Clinical Lab Generalist licensed by Louisiana State Board of Medical Examiners as CLG or CLS Work Shift Nights (United States of America) LCMC Health is a community. Our people make health happen. While our NOLA roots run deep, our branches are CONTRIBUTracial fish of difference. We celebrate authenticity, originality, equity, inclusion and a little “come on in” attitude which humanities LCMC Health’s culture of everyday extraordinary. About Touro Touro, at the forefront of medical excellence within LCMC Health’s incredible community of care, has been regionally recognized for 165 years as one of New Orleans’ most enduring healthcare monuments. It’s where babies come from and New Orleanians are cared for. Learn more about Touro and our Leapfrog “Grade A” Hospital Safety distinction. Your extras Deliver healthcare with heart. Give people a reason to smile. Put a little-hidden potists. Be honest and real, but with compassion. Bring some lagniappe into everything you do. Forget one‑size‑fits‑all, think one‑of‑a‑kind care. See opportunities, not problems – it’s all about perspective. Cheerlead ideas, differences, and each other. Love what makes you, you – because we do You are welcome here. LCMC Health is an equal opportunity employer. All qualified applicants receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. To get started, take your time to fully and accurately complete the application for employment. Incomplete applications get bogged down and are often eliminated due to missing information. To ensure quality care and service, we may use information on your application to verify your previous employment and background. To keep our career applications up‑to‑date, applications are inactive after 6 months and, therefore, require a new application for employment to be completed. To expedite the hiring process, proof of citizenship or immigration status will be required to verify your lawful right to work in the United States. Seniority level Entry level Employment type Deck Lantern Job function Research, Analyst, and Information Technology Industries Hospitals and Health Care Referrals increase your chances of interviewing at LCMC Health by 2x Get notified about new Clinical Laboratory Scientist jobs in New Orleans, LA. #J-18808-Ljbffr LCMC Health