Lead CLS (T-F, 12-10:30 PM)

Lead CLS (T-F, 12-10:30 PM) We’re growing fast. There are many opportunities for learning and career development at Octapharma Plasma. Because you’re someone who loves to learn, enjoys people, and has a real heart to help, you may join us as a Lead CLS (T-F, 12-10:30 PM). Responsibilities Performs a full range of laboratory tests, from the most routine to the most complex, with no supervision. Responsible for specimen processing, test performance and reporting test results. Performs only those high complexity tests that are authorized by the CLIA laboratory director and require a degree of skill commensurate with the individual's education, training or experience, and technical abilities. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of test results. Ability to manage individual daily workflow independently. Identify problems that may adversely affect test performance or reporting of test results and resolve the problem or bring it to the immediate attention of supervisor, manager, or director. Proficient on at least two (2) or more testing platforms; perform advanced troubleshooting on two (2) or more testing platforms. Perform FDA, CLIA, and other required tests on blood and blood products according to Octapharma Plasma approved SOPs or special protocols. May be cross-trained to perform viral marker testing, sickle cell screen, ABO/Rh/antibody detection, antibody identification and red cell phenotyping, sterility cultures, and Anti-D Titers. Operate and interact with a range of complex precision instruments and highly automated/electronic equipment. Perform glycerolyzation and deglycerolyzation procedures to prepare immunogen cell units for storage or distribution. Maintain complete and accurate records of all events, tasks and testing related to product testing and eventual release or distribution. Perform and document laboratory testing and instrument quality control, proficiency testing, preventive maintenance, troubleshooting, calibration and validation; maintain records demonstrating proficiency testing samples are tested like donor samples. Perform and document laboratory testing related to Comparability Studies between analyzers and/or methods; participate in Reagent Management (qualification, inventory oversight, lot management). Support instrument maintenance and service (removing/returning instrument from service; arrange for Technical Service as needed) and handle complex issues. Qualified to act as a General Supervisor as defined by CLIA; act as a technical advisor for other testing personnel. Participate in Laboratory Deviation Management as a Deviation Initiator and Investigator; qualify to act as a Designated Trainer for training and competency assessment. Provide on-call coverage per rotational schedule with cross-trained team members; follow approved SOPs when test systems are not within acceptable performance levels. Qualifications Ability to uphold and demonstrate OPI’s Values. Bachelor of Arts/Bachelor of Science in a laboratory science or Medical/Clinical Laboratory Science from an accredited institution. Two (2) years’ experience performing clinical laboratory tests, required. Minimum of one (1) year performing Charlotte Testing clinical laboratory scientist essential job functions required. Must qualify as a general supervisor in accordance with CLIA Regulations 493.1423 Standard; Testing Personnel Qualifications. ASCP certification or eligibility preferred. New York and California State testing requirements preferred. Ability to work diverse shifts and overtime hours, as required; ability to work in a variety of test areas after appropriate training. Self-motivated with the ability to work with minimal supervision while being flexible to changing priorities. Excellent verbal, written and interpersonal skills; ability to assist less experienced staff. Proficient with computer software in an office and laboratory environment; ability to learn applicable software for sample management, QC test result management, and drafting laboratory/QA procedures. Ability to read, understand, write, and follow SOPs/validation protocols and document accordingly; excellent organizational skills and attention to detail. Organizes time and priorities to achieve business results in a timely manner. Benefits Formal training Medical, dental, and vision insurance; health savings account (HSA) and flexible spending account (FSA) Tuition reimbursement; employee assistance program (EAP) Wellness program; 401(k) retirement plan Paid time off; company paid holidays; personal time Additional information Pay transparency: Octapharma Plasma, Inc. is growing with donation centers across the U.S. We rely on teamwork, compassion, and expertise to make a meaningful difference. Learn more online and apply at octapharmaplasma.com. #J-18808-Ljbffr Octapharma Plasma, Inc.