AbbVie logo

Production Specialist l (M-F) 2:30pm to 11:00pm

AbbVie
Full-time
On-site
North Chicago, IL
$15.50 - $28.80 USD yearly
Operations

Want to see how your resume matches up to this job? A free trial of our JobsAI will help! With over 2,000 biopharma executives loving it, we think you will too! Try it now — JobsAI.

Role Summary

Production Specialist I (M-F) 2:30pm to 11:00pm.

Responsibilities

  • Adhere to Environmental, Health and Safety procedures and guidelines, and facilitate a proactive safety culture. Use Abbvie approved tools for the job to minimize the introduction of extraneous matter into the packaging process.
  • Perform all housekeeping cleans on the finishing lines. Able to complete line clearances for lot and list changes and perform blowing of the finishing line/equipment on 1-2 value stream(s).
  • Assist in setup of automated equipment in primary or secondary packaging area within 1-2 value stream(s).
  • Servicing and operating automated and semi-automated manufacturing equipment to produce finished product on value stream(s) with the ability to complete assigned tasks with minimal supervision.
  • Perform Quality impactful tasks throughout the production run, including but not limited to challenges, parameters, pulling samples, in-process checks and bulk/commodity accountability.
  • Sustain 6S of parts and tooling across the production floor.
  • Escalate higher level safety, quality, technical and operating issues in a timely manner to the appropriate groups.
  • Communicate and drive improvement opportunities through cross functional teams. Works closely with the production schedule and understands line priorities while working with minimal/limited supervision.
  • Troubleshoots minor equipment related issues and performs minor adjustments to improve equipment efficiencies.

Qualifications

  • High school diploma or GED required.
  • Technical experience and troubleshooting aptitude preferred. Technical certificate or degree preferred.
  • Demonstrated focus and understanding of the importance of maintaining the highest level of quality and ensuring compliance to site level policies and procedures.
  • Ability to communicate issues to appropriate engineering and mechanical team required.
  • Basic computer skills and ability to learn new programs and applications required.
  • Understanding and experience with systems such as POMs, and SAP preferred.
  • Knowledge of related cGMP requirements and procedures is preferred.
  • Requires standing up to 8-12hrs per day and lifting up to 25 pounds.
  • Work 40 to 48 hours per week and may work as many as 60 hours depending on manufacturing demands.
Apply now
Share this job