Quality Auditor Associate

Responsible for testing and analyzing incoming materials, intermediates, finished products, swab samples and other samples of a moderate scope and complexity of activity. Work Schedule: 1st shift early (6 a.m. - 2:30 p.m. M-F) and 3rd shift (10 p.m. - 6:30 a.m. M-F, Onsite) Job Responsibilities: Perform sampling and delivery of intermediate and finished products. Assist with retain sample management. Conduct monthly GMP and batch-specific room audits. Perform in process record review of commercial manufacturing batch records. Review completed swab data and performed subsequent room/equipment release. Ensures compliance with all Company policies and procedures, including safety rules and regulations. Performs related duties as assigned. Skills: Requires a minimum of one year experience in a regulated environment such as pharmaceutical, medical device, nutraceutical, or food processing industries. Requires basic understanding of Good Manufacturing Practice (cGMP) and the application to a production environment. Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), EDMS and ERP systems. Education/Experience: Associate's degree or higher (or equivalent) achieved or in process preferred.