QA Inspector II - 2nd Shift, GMP Packaging

Regulatory Jobs

Piscataway Township (NJ)

On-site

USD 29,000 - 37,000

Full time

6 days ago
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Job summary

Amneal in New Jersey is seeking a QA Inspector I to support sampling, testing and inspection of incoming materials, packaging components and returns. The role requires 2+ years in QA or related fields, strong math skills, and meticulous record-keeping.

2nd shift, 3pm–11:30pm, with opportunities for growth in a GMP environment. Responsibilities include preparing samples for QC, inspecting packaging components with precision, documenting results, and ensuring compliance across manufacturing steps.

Qualifications

  • High School diploma or GED required.
  • 2+ years of QA or related field experience.
  • Good basic math knowledge and attention to detail.
  • Records observations for improving processes.

Responsibilities

  • Perform inspection, sampling and testing of incoming raw materials, packaging components and returned goods following detailed procedures.
  • Prepare samples for chemical and microbiological analysis and deliver to the QC lab.
  • Inspect packaging components using measuring devices to ensure conformance to specifications; maintain records of activities.
  • Assign and verify expiry and retest dates for GMP materials from COA sources; maintain logs.
  • Labeling components and packaging inspections; prepare reports; support batch record reconciliation and deviations.
  • Disposal of rejected material per SOP and conduct environmental monitoring as required.

Skills

Math
Attention to detail

Education

High School or GED

Job description

Amneal in New Jersey is seeking a QA Inspector I to support sampling, testing and inspection of incoming materials, packaging components and returns. The role requires 2+ years in QA or related fields, strong math skills, and meticulous record-keeping.

2nd shift, 3pm–11:30pm, with opportunities for growth in a GMP environment. Responsibilities include preparing samples for QC, inspecting packaging components with precision, documenting results, and ensuring compliance across manufacturing steps.

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