ILP Production Technician III: Visual Inspection & Packaging

QuVa - Advancing Healthcare Possibilities

Bloomsbury (NJ)

On-site

USD 28,000 - 39,000

Full time

6 days ago
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Job summary

QuVa - Advancing Healthcare Possibilities is seeking a Production Technician III – ILP to support visual inspection, labeling and packaging in a GMP-compliant facility in the United States. The role requires experience in pharmaceutical manufacturing and adherence to cGMPs and ISO standards.

The candidate will perform material prep, equipment calibration checks, and documentation, while ensuring safety and regulatory compliance.

Qualifications

  • High school Diploma or GED from recognized institution or organization required.
  • Minimum of 2 years reliable and sustained performance as a Production Technician II – ILP or pharmaceutical manufacturing experience.
  • Legally authorized to work in the job posting country.
  • Color perception exam required and must pass.
  • Vision exam required and must have 20/20 vision with or without correction.

Responsibilities

  • Support ILP operation, including visual inspection, labeling, and packaging.
  • Prepare inspection and packaging room materials and supplies.
  • Safely transport product and materials per SOP and EH&S requirements.
  • Conduct labeling and processing of production materials as required.
  • Investigate and resolve reconciliation issues to progress batches toward closure.
  • Daily/bi-weekly/monthly cleaning and preventive maintenance documentation.
  • Complete line and room clearances per procedures.
  • Document activities per GDPs; comply with cGMPs and ISO standards.
  • Maintain daily supply list and coordinate with receiving.

Skills

Communication skills
Mechanical aptitude
Attention to detail
Flexibility
Safety mindset

Education

High school diploma or GED

Tools

PacMac equipment
Labelers

Job description

QuVa - Advancing Healthcare Possibilities is seeking a Production Technician III – ILP to support visual inspection, labeling and packaging in a GMP-compliant facility in the United States. The role requires experience in pharmaceutical manufacturing and adherence to cGMPs and ISO standards.

The candidate will perform material prep, equipment calibration checks, and documentation, while ensuring safety and regulatory compliance.

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