Quality Inspector I - Precision QA (Medical Devices)

Integra LifeSciences Corporation; Northern (KY); Hybrid; USD 14,000 - 19,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Life insurance

Disability Insurance

401(k)

Job summary

Integra LifeSciences is seeking a Quality Inspector I in Kentucky to visually inspect labels, pouches and products during packing operations. The role involves sample collection, adherence to specifications, and making accept/reject decisions on process quality. It is a 2nd shift, Monday–Friday, 1:30pm–10pm.

Responsibilities include verifying dimensions with gauges, following QC procedures, and maintaining records. Training new inspectors and ensuring GMP compliance are part of the duties.

Qualifications

• High School graduate or equivalent.
• 1 year experience in FDA-regulated manufacturing preferred.
• Ability to read drawings and written procedures in English.
• Ability to use testing instruments and manual equipment.
• Must stand for long periods.

Responsibilities

• Inspect product dimensions, cavity measures, pressure and specifications with gauges and testing equipment.
• Follow inspection criteria to release or reject lots.
• Fill quality control records and maintain documentation.
• Assist in training of new QA inspectors.
• Ensure calibration of equipment and proper documentation.

Skills

Math concepts

Statistical process control

Reading drawings

Manual inspection

Standing long periods

Education

High School diploma

Tools

Optical comparator

Micrometer

Calipers

Go/no-go gauges

Job description

Integra LifeSciences is seeking a Quality Inspector I in Kentucky to visually inspect labels, pouches and products during packing operations. The role involves sample collection, adherence to specifications, and making accept/reject decisions on process quality. It is a 2nd shift, Monday–Friday, 1:30pm–10pm.

Responsibilities include verifying dimensions with gauges, following QC procedures, and maintaining records. Training new inspectors and ensuring GMP compliance are part of the duties.