Quality Inspector I - 2nd Shift (GMP)

Integra LifeSciences; Añasco (PR); On-site; USD 11,000 - 18,000; Full time

Job summary

Integra LifeSciences is seeking a Quality Inspector I to visually inspect labels, pids, and pouches, and to record data to ensure packing operations meet specifications. The role supports GMP compliance and quality control across production areas.

The position is a 2nd shift (1:30pm–10:00pm) with responsibilities including data recording, adherence to SOPs, and potential cross-workstation assignments, ensuring product quality and compliance.

Qualifications

• High School graduate or equivalent.
• One (1) year experience in a similar position in an FDA regulated manufacturing environment preferred.
• Driver's license on heavy vehicles highly preferred.
• Knowledge of basic math concepts, graph interpretation, and use of procedure, and inspection methods.
• Knowledge of statistical process control techniques.
• Ability to read, understand drawings and written documents in English.

Responsibilities

• Inspect labels, pid's and pouches visually to approve packing operations.
• Record inspection data and make accept/reject decisions based on specifications.
• Fill quality control records and maintain documentation.
• Assist in training of new QA Inspectors.
• Follow GMP/Quality Manual and conduct spot audits in manufacturing areas.
• Set up and perform destructive and non-destructive tests on materials or products.

Skills

Quality inspection

GMP compliance

Reading drawings

Math skills

Education

High School diploma

Tools

Optical comparator

Micrometer

Calipers

Go-no-go gauges

Microscope

Air pressure gauges

Job description

Integra LifeSciences is seeking a Quality Inspector I to visually inspect labels, pids, and pouches, and to record data to ensure packing operations meet specifications. The role supports GMP compliance and quality control across production areas.

The position is a 2nd shift (1:30pm–10:00pm) with responsibilities including data recording, adherence to SOPs, and potential cross-workstation assignments, ensuring product quality and compliance.