Pharma Production Technician I (3rd Shift)

AbbVie

Tempe (AZ)

On-site

USD 26,000 - 46,000

Full time

2 days ago
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Job summary

AbbVie Inc. in Tempe is seeking a Production Technician I to execute manufacturing processes in formulation, encapsulation, and packaging on a 3rd shift (Thu-Sat, with every other Wed). The role emphasizes GMP compliance, OEE targets, and timely resolution of equipment issues.

Responsibilities include line work, multi-unit operation, setup and troubleshooting of equipment, and training of colleagues. Prior cGMP manufacturing experience is preferred; basic computer skills and diligence to quality

Qualifications

  • High school diploma or GED required; technical certificate or degree preferred.
  • Strong technical aptitude and ability to troubleshoot and communicate issues to operations teams.
  • Basic computer skills and willingness to learn new programs.
  • Understanding of HMI controls, vision inspection systems, and product serialization systems.
  • Experience with SAP, MAXIMO, and POMs is a plus.

Responsibilities

  • Set up equipment for routine processes and operate line on assigned shift.
  • Monitor the manufacturing process and communicate issues to appropriate resources.
  • Perform setup, running, cleaning, and cleaning steps per batch records.
  • Conduct in-process quality checks and basic repairs.
  • Train colleagues on equipment and processes as needed.
  • Adhere to GMP, ALCOA, and safety guidelines.

Skills

Technical aptitude
Troubleshooting
Communication
HMI controls
Product serialization

Education

High school diploma or GED
Technical certificate or degree

Tools

SAP
MAXIMO
POMs

Job description

AbbVie Inc. in Tempe is seeking a Production Technician I to execute manufacturing processes in formulation, encapsulation, and packaging on a 3rd shift (Thu-Sat, with every other Wed). The role emphasizes GMP compliance, OEE targets, and timely resolution of equipment issues.

Responsibilities include line work, multi-unit operation, setup and troubleshooting of equipment, and training of colleagues. Prior cGMP manufacturing experience is preferred; basic computer skills and diligence to quality

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