Bilingual QA Inspector - Night Shift (English/Spanish)

More Results Bilingual QA Inspector - Night Shift (English/Spanish) Employer 5TH HQ Location Fort Lauderdale, Florida, US Salary Competitive Closing date Jun 3, 2026 View more categories View less categories Sector Consultancy/Private Sector Field Conservation science Discipline Biology Salary Type Salary Employment Type Full time Apply on website Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Job DescriptionJob Description Position Summary We are seeking a detail-oriented QA Inspector to join our team on the night shift. This role is responsible for performing in-process inspections, ensuring compliance with cGMP standards, and maintaining accurate documentation in accordance with internal procedures and regulatory requirements. Schedule: Monday - Friday | 9:30 PM - 5:15 AM Pay Rate: $20.37 -$22 per hour Essential Functions & Responsibilities Perform inspection of in-process and finished products, ensuring proper documentation. Ensure compliance with cGMP regulations at all times on the production floor. Conduct QA tasks including sampling, inspections, and testing to verify compliance with: Internal SOPs, Company policies, Safety initiatives, FDA and DEA regulations Inspect and approve rooms, production lines, and equipment prior to use. Approve components for in-process operations. Monitor manufacturing and packaging areas for compliance with SOPs and regulatory standards. Document all work in batch records, logs, and forms accurately and thoroughly. Sample in-process materials and finished products; distribute samples as required. Review documentation for accuracy and compliance with cGMP and Good Documentation Practices. Inform management of deviations, problems, or failures. Apply disposition status to components and in-process materials. Issue QA Alerts when questionable materials or products are identified. Perform other duties as assigned by the supervisor. Qualifications Associate degree or equivalent work experience. 1-3 years of experience in Quality Control within a manufacturing environment. Bilingual (English/Spanish) required. Knowledge of cGMP regulations and FDA guidelines. Detail-oriented with strong documentation skills. Basic computer and math skills. Share this job Facebook Twitter LinkedIn Apply on website Send job Apply on website Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert