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Packaging Associate II - 3rd Shift

Job in Macungie, Lehigh County, Pennsylvania, 18062, USA
Listing for: System One Holdings, LLC
Full Time position
Listed on 2026-07-01
Job specializations:
  • Manufacturing / Production
    Regulatory Compliance Specialist, Production QC/QA, Quality Engineering
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Production QC/QA, Quality Engineering
Salary/Wage Range or Industry Benchmark: 19 USD Hourly USD 19.00 HOUR
Job Description & How to Apply Below
Location: Macungie

Packaging Associate II - 3rd Shift

Location:

Macungie, PA 18062 Type:
Contract To Hire Compensation: $19.00/hour + $2 shift differential

Hours:

11:00PM-7:00AM, Sunday-Thursday

Overview Established and growing pharmaceutical manufacturing company is seeking to add quality minded packaging associates to their growing team.

Responsibilities

  • Ensure adherence to and enforce GMP compliance during packaging operations.
  • Perform visual, functional, destructive, and count quality inspections of units during packaging, verifying component attributes and documenting results.
  • Review and verify documentation, including batch records and component attributes, supporting compliance with regulatory requirements and customer specifications.
  • Read and understand process steps within packaging records to ensure process adherence and quality during the packaging process.
  • Assist with overall production efficiency in the assigned area, supporting team efforts to meet production goals.
  • Inspect units for quality as they are packaged, supporting quality assurance and regulatory compliance.
  • Verify the accuracy and completeness of packaging documentation, ensuring all information aligns with AQL requirements and proper support documentation is maintained.

Requirements

  • High School diploma or equivalent
  • Experience with/knowledge of GMP quality or manufacturing in a regulated environment, including visual inspections and documentation verification
  • Knowledge of cGMP (21

    CFR 210, 211, 820) and/or DEA regulations for controlled substances
  • Ability to pass a GMP assessment during orientation at the Allentown site
Position Requirements
10+ Years work experience
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