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AbbVie
Westport, Missouri, United States
(on-site)
Job Type
Full-Time
Job Function
Other
Inspection Operator
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Inspection Operator
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Description
ICompany DescriptionAbbVie'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 Tik Tok.
Job Description
If you want to be a difference maker our people are waiting. See the difference you can make at AbbVie.
We are now recruiting Inspection Operators to join our diverse team in Westport, on a 9 month contract.
As our newest operator, you will ensure the highest quality and safety compliance standards while gaining exposure to new and advanced technology in various areas of coding and packaging. You will be responsible for inspection of the product and operate high-speed equipment for the manual and/or automated inspection, coding and labelling. This role would suit career changers or anyone wishing to gain valuable experience within the pharmaceutical industry.
There are positions available on the evening shift (4:30pm-12am), night shift (12am-8am) or weekend shift (12 hours Fri-Sun, weekly rotation between days and nights). Flexibility is required.
Is this a team you want to be part of? Then read on...
Key Activities:
- Adhere to AbbVie's Safety, Environmental, and Quality policies, operating safely and following plant and departmental procedures.
- Perform assigned duties in accordance with SOPs and current Good Manufacturing Practices (cGMPs).
- Complete batch ID coding in accordance with SOP's.
- Complete final visual inspection of commercial biologics products
- Conduct in-process quality control checks in accordance with SOP's.
- Support line maintenance, including rework activities.
- Keep workstations clean, organized, and well-maintained.
- Stay up to date on job procedures through online learning system and on-the-job training.
- Complete and maintain all required cGMP and safety training.
- Engage proactively with departmental safety, quality, and 6S incentives.
Qualifications
Education, Competencies and Experience
- Leaving cert or equivalent qualification required
- Excellent attention to detail
- Knowledge of computer systems desirable but not essential
- Ability to work in a fast-paced environment, demonstrating flexibility, adaptability, and strong work ethics.
- Excellent interpersonal, communication, and written skills for effective teamwork within the department.
Be part of a company that values integrity, teamwork, and personal growth. Apply now to join our mission-driven team!
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.htmlI
Job ID: 81204676
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