LSI Staffing
Las Vegas, Nevada
Temp to Hire Dec 23, 2025
Quality Control Inspector Location:
South Las Vegas, NV Shift:
6:00 am to 2:30 pm Payrate:
$18.00
We are seeking a detail-oriented
Quality Control Inspector
to maintain excellence across our production lines in South Las Vegas. You will be responsible for approving products to specification—including labeling, filling and packaging—within a strictly regulated
FDA/cGMP
environment.
Primary Responsibilities
Inspections:
Perform First Article, in‑process and finished product inspections (visual and measurement tests).
Documentation:
Record all quality results in Device History Records (DHR) using
Good Documentation Practices (GDP) .
Testing:
Conduct bulk formulation checks and prepare production test samples using the
Neogen System .
Disposition:
Accept or reject in‑process items; segregate defects for rework or disposal.
Compliance:
Ensure all work meets
FDA (QSR/cGMP)
safety and quality standards.
Qualifications
Experience:
1+ years in a QC role (preferred).
Education:
High School Diploma or equivalent.
Skills:
Basic math, computer literacy, and strong attention to detail.
Compliance:
Knowledge of cGMP or regulated manufacturing is a plus.
Physical:
Ability to stand/walk for long periods and work the 8:00 AM – 4:30 PM shift (with overtime as required).
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Quality Control Inspector Location:
South Las Vegas, NV Shift:
6:00 am to 2:30 pm Payrate:
$18.00
We are seeking a detail-oriented
Quality Control Inspector
to maintain excellence across our production lines in South Las Vegas. You will be responsible for approving products to specification—including labeling, filling and packaging—within a strictly regulated
FDA/cGMP
environment.
Primary Responsibilities
Inspections:
Perform First Article, in‑process and finished product inspections (visual and measurement tests).
Documentation:
Record all quality results in Device History Records (DHR) using
Good Documentation Practices (GDP) .
Testing:
Conduct bulk formulation checks and prepare production test samples using the
Neogen System .
Disposition:
Accept or reject in‑process items; segregate defects for rework or disposal.
Compliance:
Ensure all work meets
FDA (QSR/cGMP)
safety and quality standards.
Qualifications
Experience:
1+ years in a QC role (preferred).
Education:
High School Diploma or equivalent.
Skills:
Basic math, computer literacy, and strong attention to detail.
Compliance:
Knowledge of cGMP or regulated manufacturing is a plus.
Physical:
Ability to stand/walk for long periods and work the 8:00 AM – 4:30 PM shift (with overtime as required).
#J-18808-Ljbffr