Label Room QA Inspector – Pharma Packaging & Compliance

PL Developments Careers

Piedmont (SC)

On-site

USD 42,000 - 63,000

Full time

8 days ago
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Benefits offered by this job

Medical and Dental Benefits
401K with employer match
Paid Time Off and Paid Holidays
Opportunities to Flourish Within the

Job summary

PL Developments is seeking a QA Label Room Inspector to ensure labeling and packaging materials meet quality standards before use in production. This on-site role requires collaboration with production and QA teams to verify accuracy, maintain compliance, and document findings.

The position emphasizes attention to detail, familiarity with GMP and FDA regulations, and ability to work in a regulated manufacturing environment. Monday–Friday schedule and full-time status are included.

Qualifications

  • High school diploma or equivalent (associate degree preferred).
  • Experience in QA, labeling, or packaging in regulated industries.
  • Strong attention to detail and error detection.
  • Familiar with GMP and FDA regulations.

Responsibilities

  • Inspect and unpack incoming labels and packaging for regulatory compliance.
  • Verify label data: product name, lot number, revision, and other required fields.
  • Print, verify, approve and issue master shipper labels as needed per schedule.
  • Maintain detailed inspection records and NCRs; document deviations.
  • Collaborate with production and QA to address labeling issues and corrective actions.

Skills

Attention to detail
Communication skills
English proficiency
Independent worker
Microsoft Office

Education

High school diploma or equivalent

Tools

Oracle
Agile

Job description

PL Developments is seeking a QA Label Room Inspector to ensure labeling and packaging materials meet quality standards before use in production. This on-site role requires collaboration with production and QA teams to verify accuracy, maintain compliance, and document findings.

The position emphasizes attention to detail, familiarity with GMP and FDA regulations, and ability to work in a regulated manufacturing environment. Monday–Friday schedule and full-time status are included.

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