<?xml version="1.0" encoding="UTF-8"?><rss version="2.0" xmlns:media="http://search.yahoo.com/mrss/"><channel><title>VitaCyte LLC Jobs</title><link>https://vitacyte-llc.prismhr-hire.com</link><description>Open positions at VitaCyte LLC</description><item><title>Quality Control Associate Scientist</title><link>https://vitacyte-llc.prismhr-hire.com/job/1066720/quality-control-associate-scientist</link><description>Job Purpose The job is primarily focused on biochemical analysis and assay of enzyme activities of products sold by an Indianapolis based biotechnology company where customers use these products to…</description><category/><location>Indianapolis, IN</location><media:description type="html"><![CDATA[<p>Job Purpose The job is primarily focused on biochemical analysis and assay of enzyme activities of products sold by an Indianapolis based biotechnology company where customers use these products to recover cells from tissue or after cell culture for research, development, or clinical applications.</p><p>Education/experience  </p><ul><li>The appropriate candidate will have an Associates’ or Bachelors’ degree in a relevant field (e.g., chemistry, biochemistry, biotechnology, or biology) from an accredited institution.  </li><li>Prefer at least one year of experience working in a laboratory setting or a minimum of three months experience in a directly related internship training position.</li></ul><p>Duties:  </p><ul><li>Preparation of biological buffers used in quality control (QC) testing  </li><li><span class="normaltextrun">Execute established kinetic and endpoint quality control enzymatic assays for quality control release of in-process or final products.</span><span class="normaltextrun"></span>  </li><li><span class="normaltextrun">Perform all QC testing with strict adherence to established procedures and policies to ensure traceability and protect the integrity of the products</span><span class="normaltextrun"></span>  </li><li><span class="eop">Properly document all QC activities in accordance with Good Documentation Practice (GDP).</span>  </li><li><span class="normaltextrun">Maintain appropriate laboratory hygiene to minimize accidents and compromising product integrity</span><span class="eop"></span>  </li><li><span class="normaltextrun">Properly maintain, calibrate, qualify and clean equipment and instruments used in the QC lab.</span><span class="eop"></span>  </li><li>Support maintenance of ISO 9001 certification, ensuring the standards are followed.</li></ul><p>Skills/Knowledge/Abilities:</p><ul><li><span class="normaltextrun">Rigorously disciplined adherence to established procedures and protocols</span><span class="eop">&nbsp;</span>  </li><li><span class="normaltextrun">Strong interpersonal skills with a strong willingness to work with others in a team setting to accomplish organizational goals</span>  </li><li><span class="normaltextrun">Detail oriented and meticulously attentive to proper handling and interpretation of raw data to obtain statistically sound results and draw sound and unbiased scientific conclusions</span><span class="eop">&nbsp;</span>  </li><li><span class="normaltextrun">&gt;span class="eop"&gt;&nbsp;</span>  </li><li><span class="normaltextrun">Proficiency with Microsoft Excel, Word and Outlook</span>  </li><li>Average physical strength is required.   </li></ul><p>Full time, permanent position including a comprehensive benefit package that includes participation in an employer matched 401K plan.</p><ul><li>Salary is commensurate with experience.&nbsp;</li></ul>]]></media:description></item></channel></rss>