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Medical Technologist III (5K Sign on exclusions apply + Relocation)

Laboratory Corporation of America Holdings (Covance)

Indianapolis, Indiana, United States

<h2>Job Overview:</h2><p style="margin: 3.85pt 2.15pt 12.0pt 0in;"><span style="font-size: 12pt; font-family: Verdana, sans-serif; color: black;">Are you interested in making a real scientific impact through your everyday work? Would you enjoy working in a team-focused environment as you explore unique career opportunities?</span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: Verdana, sans-serif; color: black;">If you are looking for a company where you can gain exposure to a wide variety of science and explore a multitude of career paths across the drug development spectrum, consider working at Covance as a Medical Technologist III. This position is located in our Indianapolis, Indiana Central Laboratory. </span></p><p style="margin-bottom: .0001pt;"> </p><p style="margin-bottom: .0001pt;"><strong><span style="font-size: 12pt; font-family: Verdana, sans-serif; color: black;">Our benefits packages offer 24 PTO days (prorated based on start date), 7 paid holidays, shift differentials, 401K plan, paid relocation, and Tuition Reimbursement. </span></strong></p><p style="margin-bottom: 0.0001pt; text-align: center;"> </p><p style="margin-bottom: 0.0001pt; text-align: center;"><span style="color: #008000; font-size: 18pt;"><strong><span style="font-family: Verdana, sans-serif;"> Medical Technologist III (1st shift) </span></strong></span></p><p style="margin: 3.85pt 2.15pt 12pt 0in; text-align: center;"><span style="color: #008000; font-size: 18pt;"><em><span style="font-family: Arial, sans-serif;">Play a pivotal role in the drug development process and grow your career</span></em></span></p><p style="margin: 3.85pt 2.15pt 12pt 0in; text-align: center;"><span style="color: #008000; font-size: 18pt;"><em><span style="font-family: Arial, sans-serif;">This position is located in Indianapolis, IN </span></em></span></p><p style="margin-bottom: 0.0001pt; text-align: center;"><strong><span style="font-size: 12pt; font-family: Verdana, sans-serif; color: black;">(5K Sign on exclusions apply + Relocation)</span></strong></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">The Technologist III will perform duties of Technologist I, or II, and may perform duties of Sr Tech in addition to the following additional duties:</span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Essential Functions</span></p><dir><dir><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">♦ Instruments/Equipment: Demonstrates thorough working knowledge of instruments/equipment in the department. Able to provide troubleshooting guidance to staff to resolve complex instrument and equipment problems. Works with the vendor where needed to resolve instrument/ equipment related problems and summarize results of investigations.</span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"> </span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">♦ Training: Coordinates the timely development and completion of training materials and checklists.</span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">o Seeks and promotes expertise in department and across sites to ensure consistent approach to training.</span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"> </span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">♦ SOP: Initiates revisions to SOPs or writes new SOPs to reflect current processes that ensure compliance. Coordinates with other departments and other sites to ensure timely completion of SOP. Resolves obstacles, where needed.</span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"> </span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">♦ Instrument/Equipment/Assay Validation: Responsible for coordinating with other resources to ensure timely completion and implementation of new assay validations.</span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">o May be asked to research, develop, validate and maintain procedures in area of responsibility and make recommendations on modification/improvement of procedures to management.</span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"> </span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">♦ Process Improvement: Able to analyze existing processes and create new approaches or ideas to improve. Works with internal/external department to ensure successful implementation of changes /improvements.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">o Demonstrates extensive knowledge of all department functions, and may serve as subject matter expert for department on company wide initiatives (i.e., Six Sigma).</span></p></dir></dir><dir><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">♦ Supports client audit process and responding to inquiries.</span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">♦ Serves as an expert in all facets of trained workstations in area of responsibility. Responds to problems or questions of department staff.</span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"> </span></p></dir><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Non-Essential Functions</span></p><dir><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">♦ Only individuals that are verified to qualify as supervisory personnel under regulations/standards applicable to the facility (e.g., New York State, CLIA, CAP) may perform periodic review and approval of quality control program records (e.g. quality control data, instrument logs, reagent logs). The SOPs applicable to the department should be consulted to determine records that can be reviewed and approved.</span></p></dir><h2>Education/Qualifications:</h2><p style="margin: 0px;">II. Experience:</p><p style="margin: 0px;">III. Education/Qualifications/Certifications and Licenses</p><p style="margin: 0px;"><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">U.</span><strong><span style="font-size: medium;">S. Requirements </span></strong></p><p style="margin: 0px;">Individual must qualify as testing personnel under the following CLIA 1988 and New York State Department of Health requirements:</p><p style="margin: 0px;"><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">• </span><em><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">Bachelor’s degree in Medical Technology or Clinical Laboratory Science or other life science with completion of at least a 12-month training program in Medical Technology. </span></em></p><p style="margin: 0px;">OR</p><p style="margin: 0px;">• <em>Bachelor’s degree in a chemical, physical or biological science from an accredited college or university and one year training and/or experience in the specialty in which testing is to be performed. Such training must be equivalent to that received in a school of Medical Technology. </em></p><p style="margin: 0px;">OR</p><p style="margin: 0px;"><span style="font-family: Arial,Arial; font-size: medium;">• </span><em><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">90 semester hours from an accredited institution that include the following: </span></em></p><p style="margin: 0px;">Revised: 11 Dec 2020 Page 6 of 7</p><p style="margin: 0px;">1) 16 semester hours of biology courses, which are pertinent to the medical sciences</p><p style="margin: 0px;">2) 16 semester hours of chemistry (at least 6 semester hours of Inorganic Chemistry)</p><p style="margin: 0px;">3) 3 semester hours of math</p><p style="margin: 0px;"><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">• <em>Completed an accredited clinical laboratory training program, or one year documented laboratory training or experience in the specialty that testing is to be performed. </em></span></p><p style="margin: 0px;">OR</p><p style="margin: 0px;"><span style="font-family: Arial,Arial; font-size: medium;">• </span><em><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">Associate’s degree in medical laboratory technology </span></em></p><p style="margin: 0px;">NOTE: Technologist IIIs who perform supervisory function must qualify as NYS Supervisor under Title 10 NYCRR Part 58-1.3, which includes, but is not limited to the following:</p><p style="margin: 0px;"><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">The supervisor is qualified as a medical technologist pursuant to the provisions of section 58-1.5(b) and has had at least six years of pertinent clinical laboratory experience subsequent to qualifying of which at least two years have been spent working in a clinical laboratory having a director at the doctoral level. The clinical laboratory or blood bank shall be part of a hospital, university, health department, medical research institution or other institution which provides equivalent training</span><span style="font-family: Arial,Arial; font-size: medium;">. </span></p><p style="margin: 0px;">European Requirements</p><p style="margin: 0px;"><span style="font-size: medium;">• </span><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">Medical Technologist (CFC holder) </span></p><p style="margin: 0px;">OR</p><p style="margin: 0px;"><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">• </span><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">Pharmaceutical Biology Technologist (CFC holder) </span></p><p style="margin: 0px;">OR</p><p style="margin: 0px;"><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">• </span><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">Medical Technologist (Swiss State School of Medical Technologist Degree holder) </span></p><p style="margin: 0px;">OR</p><p style="margin: 0px;"><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">• </span><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">Medical Technologist (BTS, DUT, IUT Degree holder) </span></p><p style="margin: 0px;">OR</p><p style="margin: 0px;"><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">• </span><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">Foreign Medical Technologist Degree holder with equivalency statement from Swiss Red Cross </span></p><p style="margin: 0px;">Singapore Requirements</p><p style="margin: 0px;"><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">Bachelor’s degree in a bio-medical, physical or biological science from an accredited college or university </span><strong><span style="font-size: medium;">and </span></strong><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">one year training and/or experience in the specialty in which testing is to be performed.</span></p><p style="margin: 0px;">China Requirements</p><p style="margin: 0px;">Required:</p><p style="margin: 0px;"><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">• </span><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">Bachelor's degree in Medical Technology or completion of at least a 12-month training program in Medical Technology. </span></p><p style="margin: 0px;">OR</p><p style="margin: 0px;"><span style="font-family: Arial,Arial; font-size: medium;">• </span><span style="font-family: Times New Roman,Times New Roman; font-size: medium;">Bachelor's degree in a chemical, physical or biological science from an accredited college or university and one year training and/or experience in the specialty in which testing is to be performed. Such training must be equivalent to that received in a school of Medical Technology. </span></p><p style="margin: 0px;">Japan Requirements</p><p style="margin: 0px;">Required:</p><p style="margin: 0px;">• Bachelor’s degree in biological, chemical, physical, agricultural or pharmaceutical sciences from an accredited college or university.</p><p style="margin: 0px;">OR</p><p style="margin: 0px;">• Licensed clinical laboratory technician or licensed health laboratory technician.</p><p style="margin: 0px;"> </p><h2>Experience:</h2><p style="margin: 0px;">Minimum Required:</p><p style="margin: 0px;">Individual must have 3 or more years of Covance Laboratory experience performing clinical laboratory testing or experience in performing clinical laboratory testing judged as equivalent.</p>

Job posted: 2021-04-28

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