How to Maximize your opportunity to do rewarding work, your future leadership potential, and your career growth? Join an industry leader. [Become one, too!]   We are seeking a second shift Clinical Lab Scientist to assist in growing our new, state of the art laboratory. This lab is slated to test over 4 million samples annually. Reporting into the Laboratory Operations Supervisor, this position will perform routine and specialty laboratory tests and prepare immunogen cells.    Lead Clinical Lab Scientist (Blood Bank)   This Is What You’ll Do: 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. Ability to 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 the following: Viral marker testing Syphilis screen Sickle cell screen Total protein Protein electrophoresis ABO, Rh, antibody detection, antibody identification and red cell phenotyping Sterility cultures Anti-D Titers Nucleic Acid Testing (NAT) Operate and interact with an array of complex precision instruments and a variety of highly automated and 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 as required. Maintain records that demonstrate proficiency testing samples are tested in the same manner as donor samples. Perform and document laboratory testing associated with Comparability Studies between Analyzers and/or Methods. Participate in Reagent Management including: reagent qualification, inventory oversight and lot management. Supports instrument maintenance and service by: Removing instrument from service Returning instrument from service Arrange for Technical Service, as needed Handles and coordinates complex issues Qualify to act as a General Supervisor as defined by CLIA. Evaluate and identify potential improvements for testing, production, and validation protocols. Write and revise standard operating procedures and forms as needed. Act as technical advisor for other testing personnel. Participate in Laboratory Deviation Management as a Deviation Initiator and Investigator. Qualify to act as a Designated Trainer: process, evaluate and document initial training and competency assessment of other testing personnel. Provide on call coverage per rotational schedule along with other cross trained individuals as needed. Follow Octapharma Plasma approved SOPs whenever test systems are not within the laboratory’s established acceptable levels of performance. Provide supervision in supervisor’s absence over the technical and operational staff in the laboratory area. Offer subject matter expertise in SOP development/revisions and project initiatives. Process, evaluate and document initial training and competency assessment of testing and processing personnel. Collaborates with supervisor to improve operational efficiency; develops and implements recommendations to improve operations and optimize customer service. Participates in hiring process: interview applicants and final selection. Actively participates in staff coaching and development. Manage and direct daily laboratory workflow to optimize productivity. Participates in daily sample reconciliation and evaluation of pending reports. Develops and collaborates with supervisor daily scheduling of tasks and staff responsibilities. Provide Quality Assurance support to OPI Laboratory Operations by: Ensuring corrective and preventive actions are followed, developed, and implemented in accordance with the Error Management System. Performing the Quality review of testing and instrument quality control, preventive maintenance, and calibration records, as required. Complete other duties as assigned by supervisors, managers, or director. This Is Who You Are: A natural leader who displays strong character and integrity An excellent communicator, interviewer, and presenter A person committed to excellent customer service all day, every day Outgoing, personable, energetic, and enthusiastic Excited to teach, learn, and advance with a growing organization Self-motivated and willing to assume the initiative Attentive to every detail Capable of thriving with little supervision This Is What It Takes: Ability to uphold and demonstrate OPI’s Values. Bachelor of Arts/Bachelor of Science degree 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 different test areas as required after appropriate training. Self-motivated with the ability to work with minimal supervision while able to take direction. Able to be flexible to changing priorities. Excellent verbal, written and interpersonal skills, including the ability to assist less experienced staff. Proficient with computer software in an office and laboratory environment. Has the knowledge of or ability to learn applicable software used in the course of the job: sample management, sample, and QC test result management, drafting laboratory or QA procedures and other tasks as required. Ability to read, understand, write, and follow SOPs, validation protocols, etc. and to complete documentation in a clear, accurate manner. Excellent organizational skills, provides direction to others, and strong attention to detail. Organizes time and priorities to achieve business results in a timely manner. Understands the importance of mentoring and coaching employees. Shows enthusiasm for helping Do Satisfying Work. Earn Real Rewards and Benefits.   We’re widely known and respected for our benefits and for leadership that is supportive and hands-on. Formal training Outstanding plans for medical, dental, and vision insurance Health savings account (HSA) Employee assistance program (EAP) Wellness program 401 (k) retirement plan Paid time off Company-paid holidays Personal time More About Octapharma Plasma, Inc.   With donation centers and team members throughout the U.S., Octapharma Plasma, Inc. collects plasma to create life-saving medicines for patients worldwide. We are growing at an impressive pace, and so is the positive impact of our work. Our community relies on teamwork, compassion, and expertise to get things done the right way, while making a meaningful difference in the lives we touch.   Interested? Learn more online and apply now at:   octapharmahiring.com
And if you know someone else who’d be a great fit at Octapharma Plasma, Inc., please forward this posting along.   INNER SATISFACTION. OUTSTANDING IMPACT.