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    "requisitionDescription": "<div><p data-pasted=\"true\"><strong>Position Summary&nbsp;</strong></p><p style=\"margin-left:0in;\">Responsible for performing processing/manufacturing activities of Human Transplant Tissues and devices in an FDA regulated GMP facility.</p><p style=\"margin-left:0in;\"><strong>&nbsp;</strong></p><p><strong>Essential Duties &amp; Responsibilities&nbsp;</strong></p><div style=\"margin-left:0in;\"><ul style=\"list-style-type: disc;margin-left: 0in;\"><li style=\"margin-left:0in;\">Prepare processing solutions and storage media.</li><li style=\"margin-left:0in;\">Thaw and process frozen placental tissues into finished products.</li><li style=\"margin-left:0in;\">Perform production control on 100% of units manufactured, packaged and labeled.</li><li style=\"margin-left:0in;\">Initiate processing area set up and change over as needed.</li><li style=\"margin-left:0in;\">Conduct line clearance, equipment cleaning and facility cleaning as needed.</li><li style=\"margin-left:0in;\">Perform final product label creation, verification and labeling.</li><li style=\"margin-left:0in;\">Store final product in designated quarantine areas.</li><li style=\"margin-left:0in;\">Complete documentation (e.g. batch records, cleaning logs, etc.) for review.</li><li style=\"margin-left:0in;\">Maintain aseptic and/or neat work environments.</li><li style=\"margin-left:0in;\">Prepare disinfectant for equipment and Facility cleaning as necessary.</li><li style=\"margin-left:0in;\">Complete requisitions for quality control samples and submit to the designated lab for bio-burden testing.</li><li style=\"margin-left:0in;\">Provide information as needed to assist with investigations.</li><li style=\"margin-left:0in;\">Document/report equipment and facility problems and any potential deviation during processing.&nbsp;</li></ul></div><p><strong>&nbsp;</strong></p><p><strong>Skills &amp; Abilities</strong></p><p>Essential Duty Definition:</p><div style=\"margin-left:0in;\"><ul style=\"list-style-type: disc;margin-left: 0in;\"><li style=\"margin-left:0in;\">Excellent communication skills; fluent (oral/written) English.</li><li style=\"margin-left:0in;\">Ability to multi-task, setting priorities effectively to produce quality work in a fast-paced professional environment</li><li style=\"margin-left:0in;\">Communicates effectively and appropriately. Uses good judgment as to what to communicate to whom as well as the best way to get that accomplished. Speaks in a clear and credible manner, selecting the right tone for the situation and audience. Listens to others and allows them to make their point.</li><li style=\"margin-left:0in;\">Proficient in Microsoft software applications: Excel, Word, PowerPoint and Outlook.</li><li style=\"margin-left:0in;\">Familiarity with American Association of Tissue Banks, Good Manufacturing Practices (GMP), and Hazard Analysis a plus.</li></ul></div><p><strong>&nbsp;</strong></p><p><strong>Position Expertise/Qualifications&nbsp;</strong></p><div style=\"margin-left:0in;\"><ul style=\"list-style-type: disc;margin-left: 0in;\"><li style=\"margin-left:0in;\">High School Diploma, required</li><li style=\"margin-left:0in;\">Associate&rsquo;s Degree in Biotechnology, Life Sciences, or Surgical Technology, preferred.</li><li style=\"margin-left:0in;\">6 months experience in<ul style=\"list-style-type: circle;\"><li>Biotech, laboratory or other science, required</li><li>Manufacturing in a GMP environment, required</li></ul></li></ul></div><p><strong>&nbsp;</strong></p><p><strong>Physical Requirements</strong></p><div style=\"margin-left:0in;\"><ul style=\"list-style-type: disc;margin-left: 0in;\"><li style=\"margin-left:0in;\">Sedentary work that generally requires sitting and/or standing</li></ul></div></div>\n",
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