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Bilingual QA Inspector Night Shift EnglishSpanish

Job in Fort Lauderdale, Broward County, Florida, 33336, USA
Listing for: 5TH HQ
Full Time position
Listed on 2026-07-01
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 19.45 - 21 USD Hourly USD 19.45 21.00 HOUR
Job Description & How to Apply Below

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 | 10:00 PM – 5:45 AM
Pay Rate: $19.45 –$21 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.
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