Second-Shift Quality Inspector I: Precision & GMP

Integra LifeSciences Corporation; United States; Hybrid; USD 14,000 - 19,000; Full time

Job summary

Integra LifeSciences Corporation is seeking a Quality Inspector I to visually inspect labels, pids, and pouches, approving packing operations and other processes. You will collect samples, inspect against specs, and document results to support release decisions.

This 2nd shift role (Mon-Fri, 1:30pm–10:00pm) requires attention to detail, reading specifications, and proficiency with inspection tools. Prior FDA-regulated experience is preferred.

Qualifications

• High School diploma or equivalent.
• One year of experience in a similar role in an FDA-regulated environment preferred.
• Knowledge of basic math concepts, graph interpretation and inspection methods.
• Knowledge of statistical process control techniques.
• Ability to read and interpret drawings and written procedures in English.

Responsibilities

• Inspect labels, pids and pouches visually to approve packing operations.
• Record inspection data and make accept/reject decisions based on specifications.
• Fill quality control records and assist in training new QA Inspectors.
• Maintain calibration and documentation; ensure GMP/Quality Manual reinforcement.

Skills

Quality inspection

FDA environment

Math basics

Statistical process control

Reading drawings

Testing instruments

English reading/writing

Stand for long periods

High School diploma

Heavy vehicle license

Education

High School diploma or equivalent

Tools

Measuring gauges

Optical comparator

Micrometer

Calipers

Go-no-go gauges

Pin gauges

Microscope

Air pressure gauges

Job description

Integra LifeSciences Corporation is seeking a Quality Inspector I to visually inspect labels, pids, and pouches, approving packing operations and other processes. You will collect samples, inspect against specs, and document results to support release decisions.

This 2nd shift role (Mon-Fri, 1:30pm–10:00pm) requires attention to detail, reading specifications, and proficiency with inspection tools. Prior FDA-regulated experience is preferred.