Pilot Plant Technician II — Pharma Manufacturing

AbbVie Inc.

Chicago (IL)

On-site

USD 60,000 - 85,000

Full time

12 days ago

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Benefits offered by this job

Paid time off
Medical insurance
401(k)

Job summary

AbbVie Inc. seeks an experienced Manufacturing Operator/Technician to support pharmaceutical production at our Chicago-area facilities.

You will follow GMP policies, document data, and monitor equipment to ensure clean, compliant operations. The role requires at least 5 years in manufacturing within pharma, strong troubleshooting and validation experience, and the ability to work independently while communicating deviations clearly.

Qualifications

  • Minimum of 5 years of manufacturing experience in pharmaceutical or similar environments.
  • Experience with validation, troubleshooting, and document management is required.
  • Strong technical background and ability to read and follow procedures.
  • Ability to explain deviations in writing clearly and accurately.
  • Basic math skills and problem solving; work independently.
  • Proven track record in completing technician tasks after training.

Responsibilities

  • Learn and follow department policies and SOPs; document data per GMP.
  • Note quality issues and address with appropriate personnel.
  • Review procedures and batch records; suggest improvements.
  • Inspect equipment and sign off status reports at end of process.
  • Assist engineering and validation groups to implement new equipment.
  • Coordinate with warehouse for proper staging and supplies.

Skills

Manufacturing experience
Validation
Technical troubleshooting
Documentation
Independent work

Education

High school diploma
Bachelor’s or Associate’s degree in scientific field desirable

Job description

AbbVie Inc. seeks an experienced Manufacturing Operator/Technician to support pharmaceutical production at our Chicago-area facilities.

You will follow GMP policies, document data, and monitor equipment to ensure clean, compliant operations. The role requires at least 5 years in manufacturing within pharma, strong troubleshooting and validation experience, and the ability to work independently while communicating deviations clearly.

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