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Production Technician I, Clinical Supply Packaging

Employer
AbbVie
Location
Lake County, IL, United States
Start date
Sep 19, 2020

Job Details

About AbbVie
AbbVie's mission is to discover and deliver innovative medicines 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, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .

The Production Technician I will work in a high performing and fast-paced pharmaceutical packaging operation in order to meet our production requirements while maintaining the utmost focus on safety and quality. He or she will support setup, changeover, and packaging of pharmaceutical products. He or she will be expected to contribute to and build a team environment by working together with his or her peers daily on a packaging line. He or she will be responsible for creating a quality-focused environment by motivating/influencing others and always driving for excellence within his or her team.
  • 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 packaging line/equipment on 1-2 value stream(s).
  • Setup and troubleshoot automated equipment in primary and secondary packaging area within 1 value stream. Performs vision system tasks at the mechanic level. Responsible for proper handling and disposition of commodities used during setup and troubleshooting to minimize MUV.
  • Servicing and operating automated and semi-automated manufacturing equipment to produce finished product on 1-2 value stream with the ability to complete assigned tasks with minimal supervision.
  • Perform and document Quality impactful tasks throughout the production run, including but not limited to challenges, parameters, pulling samples, in-process checks and bulk/commodity accountability.
  • Identify and assist in implementation of continuous 6S of parts and tooling across the production floor.
  • Escalate safety, quality, technical and operating concerns and ideas 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. Communicates issues and shares learning experiences through maintenance communications.
  • Initiates work orders in the CMMS (Maximo) for repairs/improvements to be planned and scheduled.
  • Fully capable in troubleshooting and resolving equipment related setup and runtime issues. Ability to escalate and communicate to Engineering or Maintenance appropriately if further troubleshooting and repairs are required.

Qualifications
  • High school diploma or equivalent experience. Technical certificate or degree preferred. Technical experience and troubleshooting aptitude preferred. Proficient at Production Specialist I or equivalent work experience.
  • Ability to communicate issues to appropriate operations, engineering and mechanical team required.
  • A demonstrated focus and understanding of the importance of maintaining the highest level of quality and ensuring compliance to site level policies and procedures.
  • Understanding of HMI controls, vision inspection systems, and product serialization systems in order to troubleshoot and resolve inefficiencies in a timely manner.
  • Basic computer skills and ability to learn new programs and applications required.
  • Understanding and experience with systems such as POMs, SAP, and MAXIMO preferred.
  • 3-4 years of knowledge of related cGMP requirements and procedures is preferred.
  • Requires standing up to 8-12hs per day and lifting up to 25 pounds.
  • Work 40 to 48 hours per week and may work overtime hours depending on manufacturing demands.

Significant Work Activities
Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel
No
Job Type
Experienced
Schedule
Full-time
Job Level Code
IC
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

Company

AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, and YouTube.

Stock Symbol: ABBV

Stock Exchange: NYSE

Company info
Website
Phone
1-800-255-5162
Location
1 North Waukegan Road
North Chicago
Illinois
60064
US

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