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Production Technician l

AbbVie Inc

North Chicago (IL)

On-site

USD 40,000 - 70,000

Full time

3 days ago
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Job summary

An established industry player is seeking a Production Technician I to join their dynamic team. This role involves executing critical manufacturing processes while adhering to strict GMP guidelines. You will be responsible for equipment setup, operation, and quality checks, ensuring compliance with safety and quality standards. Ideal candidates will possess a strong technical aptitude and effective communication skills, with a preference for those who have experience in cGMP environments. Join a company that values teamwork and quality, and make a significant impact on the production of innovative medicines.

Qualifications

  • 2-3 years of cGMP manufacturing experience preferred.
  • Understanding of quality standards and compliance.

Responsibilities

  • Execute manufacturing processes in formulation and packaging.
  • Perform minor troubleshooting and repairs on equipment.

Skills

Troubleshooting Skills
Communication Skills
Technical Aptitude

Education

High School Diploma or GED
Technical Certificate or Degree

Tools

HMI Controls
SAP
MAXIMO

Job description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and TikTok.

Job Description
Purpose

Describe the primary goals, objectives, functions, or outputs of this position.

The Production Technician I executes manufacturing processes in formulation, encapsulation, primary and secondary packaging with oversight by supervision. Sets up equipment for routine processes. Identifies and resolves performance-related equipment issues in a timely and efficient manner while adhering to GMP guidelines and procedures to meet or exceed target OEE. Executes assigned jobs and maintains operating conditions within the desired range. Communicates all operational events and issues with appropriate individuals. Identifies opportunities for improvement throughout operations and assists in implementing changes both in physical operations and written documents. Demonstrates AbbVie behaviors.

Responsibilities

List up to 10 main responsibilities for the job, including accountability and scope:

  • Proficient in team member responsibilities or equivalent. Knowledgeable of basic jobs in assigned area and GMP policies. Demonstrates compliance with local and industry quality and safety standards.
  • Work directly on the line, executing scheduling priorities, daily assignments, and production expectations. Operate multiple unit operations proficiently. Monitor manufacturing processes and communicate issues promptly.
  • Responsible for equipment setup, operation, cleaning, and clearing according to batch records.
  • Perform minor troubleshooting and repairs on equipment and processes. Conduct in-process quality checks accurately.
  • Train colleagues on equipment and processes as a qualified trainer.
  • Demonstrate AbbVie behaviors: good attendance, teamwork, respectful communication, positive attitude.
  • Follow all EHS procedures and participate in safety initiatives.
  • Complete batch record steps following ALCOA and GMP standards. Maintain audit-ready production areas and comply with regulations and policies.
Qualifications

List required and preferred qualifications (up to 10):

  • High school diploma or GED required; technical certificate or degree preferred. 2-3 years of cGMP manufacturing experience preferred.
  • Strong technical aptitude with troubleshooting skills and ability to communicate issues effectively.
  • Basic computer skills and ability to learn new applications.
  • Understanding of quality standards and compliance.
  • Knowledge of HMI controls, vision inspection, and serialization systems.
  • Experience with systems like POMs, SAP, MAXIMO is preferred.
  • Ability to stand for 8-12 hours and lift up to 25 pounds.
Additional Information

Details about compensation, benefits, and legal notices are included, emphasizing that pay ranges are estimates and vary by location, and that AbbVie is an equal opportunity employer.

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