Job Type. Full-time. Description. Position Summary. Specialist III QA is a regular employee in a full-time exempt position at Kashiv Biosciences. The responsibility for document management lies with this role, including issuance and retrieval of logbooks, laboratory notebooks, issuance of protocol and report numbers, and management of documentation. The employee will support the activities of the QA department in review of QC data and reports, an...
Prior experience working in Supplier Quality. Excellent technical writing skills. Prior experience initiating/writing, evaluating and completing Corrective and Preventive Actions (CAPA). Work experience in an FDA-regulated environment. Familiarity with CFR 820, ISO 9001:2015, and ISO 13485:2016. . Strong background in Data Analytics. . Strong experience in PowerBI (Dashboard creation, data visualization). Preferred Experience. Certified Lead (Ext...
Prior experience working in Supplier Quality. Excellent technical writing skills. Prior experience initiating/writing, evaluating and completing Corrective and Preventive Actions (CAPA). Work experience in an FDA-regulated environment. Familiarity with CFR 820, ISO 9001:2015, and ISO 13485:2016. . Strong background in Data Analytics. . Strong experience in PowerBI (Dashboard creation, data visualization). Preferred Experience. Certified Lead (Ext...
