Label Room QA Inspector I (Entry-Level)

PAI Pharma; Greenville (SC); On-site; USD 35,000 - 50,000; Full time

Job summary

PAI Pharma in Greenville, SC is seeking a Plant Quality Label Room Inspector I to inspect incoming labeling components and manage labeling operations and inventory.

You will stage items, count materials under an AQL plan, document results, and maintain clean, organized work areas while complying with cGMP and FDA regulations.

This full-time role requires basic computer skills, physical stamina, and the ability to work overtime as needed.

Qualifications

• High School Diploma or GED; 1+ years QA experience in a manufacturing environment preferred.
• Ability to work first shift and overtime as required.
• Ability to perform physical tasks of sampling and inspecting.
• Must be organized, reliable and detail oriented.
• Ability to multi-task and prioritize effectively.
• Must be able to lift and carry 30 lbs.

Responsibilities

• Sample and inspect incoming labeling components using an electronic inspection system; document results.
• Stage labeling items per the packaging schedule for all buildings.
• Count labeling materials per an AQL Sampling Plan and enter counts in spreadsheets.
• Dispose components per specifications and perform related computer transactions.
• Maintain clean, orderly work areas and ensure proper labeling and storage.
• Perform inventory reconciliations and report discrepancies to Manager.
• Develop knowledge of cGMPs, SOPs, and FDA regulations.
• Perform other related duties as required.

Skills

QA experience

Detail-oriented

Multi-tasking

Organized

Attention to safety

Education

High School Diploma or GED

Tools

MS Word

MS Excel

Barcode scanner

Scale/Balance

Fork lift

Job description

PAI Pharma in Greenville, SC is seeking a Plant Quality Label Room Inspector I to inspect incoming labeling components and manage labeling operations and inventory.

You will stage items, count materials under an AQL plan, document results, and maintain clean, organized work areas while complying with cGMP and FDA regulations.

This full-time role requires basic computer skills, physical stamina, and the ability to work overtime as needed.