QA Documentation Specialist

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    "description_html": "<p><br></p><p><strong>VISA SPONSORSHIP NOT AVAILABLE</strong></p><p><br></p><p>Kashiv BioSciences is a fully integrated biosciences company with an expanded and dynamic platform for growth including advanced drug delivery technologies, biosimilars, prodrugs, and a large development pipeline. We are looking for a Documentation Specialist to join our Piscataway NJ Quality Management team.&nbsp;</p><p>This is an exciting opportunity to work closely with Management on all aspects of Quality related to our pharmaceutical manufacturing site. Will work as a member of the Quality team to ensure GMP documents &amp; quality standards.</p><p>&nbsp;</p><p><strong>ESSENTIAL RESPONSIBILITIES</strong></p><ul><li>Perform Issuance, Archival and maintain of all GMP documents like SOP, Batch Record, Forms. &nbsp;</li><li>Maintain OOS, Deviation, &nbsp;CCF, CAPA log</li><li>Review Cross Functional departments SOP</li><li>Perform batch related sampling</li><li>Assist in batch record review&nbsp;</li><li>To train cross functional team on GDP and cGMP</li><li>To perform additional work assigned by supervisor as and when required</li></ul>",
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