Quality Inspector I — GMP & QA Specialist

Integra-Lifesciences

Añasco (PR)

On-site

USD 22,000 - 28,000

Full time

14 days+
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
Life insurance
Disability insurance
401(k) savings plan

Job summary

Integra LifeSciences is seeking a Quality Inspector I to visually inspect labels, pouches, and products, recording data and making accept/reject decisions to ensure conformance with specifications.

The role is 2nd shift, Monday to Friday, with opportunities to train fellow QA Inspectors, support GMP practices, and assist in maintaining calibration and documentation in a cleanroom environment.

Qualifications

  • High School diploma or equivalent.
  • One year experience in a similar FDA-regulated manufacturing environment preferred.
  • Driver's license on heavy vehicles highly preferred.

Responsibilities

  • Inspect dimensions, cavity measures, pressure, and other specifications using gauges and testing equipment; record inspection data.
  • Verify and release or reject lots based on inspection criteria and procedures.
  • Fill quality control records and maintain documentation.
  • Assist in training of new QA Inspectors and reinforce GMP standards.
  • Perform both destructive and non-destructive testing as required.
  • Maintain calibrated equipment and clean, organized work areas.
  • Follow Clean Room Rules and Gowning Practices.

Skills

Quality inspection
Measuring instruments
Reading drawings
Statistical process control
English literacy
Standing for long periods
Forklift operation

Education

High School diploma or equivalent

Tools

Forklift operation
Testing instruments

Job description

Integra LifeSciences is seeking a Quality Inspector I to visually inspect labels, pouches, and products, recording data and making accept/reject decisions to ensure conformance with specifications.

The role is 2nd shift, Monday to Friday, with opportunities to train fellow QA Inspectors, support GMP practices, and assist in maintaining calibration and documentation in a cleanroom environment.

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