Summary from listing
The Quality Control Associate performs receiving, start-up, in-process, and final inspections; analytical testing; batch-production-record reviews; nonconformance, deviation, and quality-documentation preparation; expiration and retest database maintenance; and troubleshooting of production and inspection issues. The role is fully on-site, requires less than three years of experience, and follows a rotating Saturday–Tuesday shift from 5:45 PM to 6:00 AM. A high school education is required, while FDA and ISO quality-system knowledge, Microsoft Office, QMS systems, and GMP experience are preferred.
