Bilingual QA Inspector (cGMP) – Davie, FL, 1st Shift

5TH HQ

Fort Lauderdale (FL)

On-site

USD 51,577,344 - 68,769,792

Full time

14 days+
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Job summary

5TH HQ is seeking a bilingual QA Inspector in Davie, FL to join a cGMP manufacturing environment. The role emphasizes attention to detail, documentation accuracy, and regulatory compliance, with a shift schedule from early morning to early afternoon.

The position is full-time with temp-to-hire potential. The ideal candidate has 1–3 years QA/QC experience, familiarity with GDP, cGMP, and FDA regulations, and the ability to operate pallet jacks.

Qualifications

  • Associate degree or equivalent work experience.
  • 1–3 years of QA/QC in a manufacturing environment.
  • Previous warehouse experience preferred.
  • Bilingual English/Spanish required.
  • Knowledge of cGMP regulations and FDA guidelines.
  • Detail-oriented with strong documentation skills.
  • Basic computer and math skills.

Responsibilities

  • Inspect in-process products and complete documentation.
  • Ensure cGMP compliance on the production floor.
  • Perform QA tasks, sampling, inspections, and testing per SOPs and FDA/DEA regs.
  • Document work activities in batch records and logs.
  • Inform management of deviations from standards.
  • Inspect rooms, lines, and equipment prior to use.
  • Review records for GDP and cGMP compliance.
  • Apply disposition status to components and materials.
  • Issue QA alerts when issues are identified.
  • Perform other duties as assigned by supervisor.

Skills

Bilingual English/Spanish
Detail oriented
Quality Assurance
cGMP knowledge
Documentation
Data entry
Math skills

Education

Associate degree

Tools

Pallet jack

Job description

5TH HQ is seeking a bilingual QA Inspector in Davie, FL to join a cGMP manufacturing environment. The role emphasizes attention to detail, documentation accuracy, and regulatory compliance, with a shift schedule from early morning to early afternoon.

The position is full-time with temp-to-hire potential. The ideal candidate has 1–3 years QA/QC experience, familiarity with GDP, cGMP, and FDA regulations, and the ability to operate pallet jacks.

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