Quality Analyst - 3rd shift

Role: Quality Analyst responsible for performing QC inspections of medical devices and tissue products, ensuring compliance with FDA, ISO, and GMP standards. Responsibilities include reviewing batch records, managing CAPA and NCR records, conducting incoming, in-process, and finished product inspections, and supporting regulatory audits. Requirements: Bachelor's in Life Science or related field preferred; 0-2 years industry experience in medical device, tissue, or pharmaceutical manufacturing; familiarity with ANSI/ASQ Z1.4-2003 and Quality System elements; ability to work 3rd shift (11pm-7:30am). HighValue: Medical Devices, Human Tissue Products, FDA-regulated environment, GMP, QC inspections, batch documentation, CAPA/NCR management, regulatory audits. WorkSetup: Vandalia, OH; 3rd shift; shift differential pay; salary range $56,730–$70,900; comprehensive benefits.