QA Specialist III - (Richmond, VA)

QA Specialist III FAREVA is currently seeking an experienced QA Specialist III to join our team in Richmond, VA. Job details: This position will perform cGMP audit activities and supplier management activities for Fareva. Audit activities includes facilitating 3rd party audits, including customer audits and FDA or other BOH inspections. Audit activities also includes conducting Internal and External audits; which involves, audit planning, audit reporting and tracking CAPA completion for audit observations. Supplier Management activities includes ensuring suppliers are appropriately qualified; which involves ensuring supplier audits are completed, supplier assessments are appropriately completed, Quality Agreements are written and established and Supplier Qualification documents are appropriately completed or updated. Ultimately, this position will help ensure drugs and cosmetics are manufactured and packaged in compliance with the applicable regulations and in compliance with cGMPs.