GMP Production Technician - 3rd Shift

BioSpace; North Chicago (IL); On-site; USD 28,000 - 33,000; Full time

Job summary

AbbVie is seeking a Production Technician I in North Chicago to execute manufacturing processes across formulation, encapsulation, and packaging with supervision. You will set up, run, and troubleshoot equipment, while ensuring GMP and safety standards are met.

The role requires 2-3 years of cGMP manufacturing experience, a strong technical aptitude, and the ability to train others. You will contribute to achieving target OEE and maintain quality documentation in a fast-paced environment.

Qualifications

• High school diploma or GED required.
• Technical certificate or degree preferred.
• 2-3 years cGMP manufacturing experience preferred.
• Strong technical aptitude; ability to troubleshoot.
• Basic computer skills and ability to learn new programs.
• Familiarity with POMs, SAP and MAXIMO.
• Ability to stand 8-12 hours and lift up to 25 pounds.

Responsibilities

• Set up and operate manufacturing equipment across formulation, encapsulation, and packaging.
• Monitor line performance and resolve issues to meet targets (OEE).
• Perform in-process quality checks; maintain ALCOA and GMP compliance.
• Train colleagues on equipment and processes; share knowledge.
• Follow safety and environmental policies; keep audit-ready production areas.

Skills

GMP compliance

Troubleshooting

Equipment operation

Team collaboration

Education

High school diploma or GED

Technical certificate or degree

Tools

SAP

MAXIMO

HMI controls

Vision inspection systems

Product serialization systems

POMs

Job description

AbbVie is seeking a Production Technician I in North Chicago to execute manufacturing processes across formulation, encapsulation, and packaging with supervision. You will set up, run, and troubleshoot equipment, while ensuring GMP and safety standards are met.

The role requires 2-3 years of cGMP manufacturing experience, a strong technical aptitude, and the ability to train others. You will contribute to achieving target OEE and maintain quality documentation in a fast-paced environment.