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Location
In office (Westport)
Seniority
Junior
Visa
Irish employment permits in the past two years
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 11, 2026. First seen by Alion on Nov 10, 2026. AbbVie scores B on the Alion truth index.

Overview
Company
Impact
Profile match
AbbVie is an American biopharmaceutical company created in 2013 when Abbott Laboratories separated its research-based drug business into a standalone listed company. It was built around the immunology drug Humira, once the highest selling medicine in the world, and has since replaced that revenue with the successor immunology drugs Skyrizi and Rinvoq, an oncology portfolio led by Imbruvica and Venclexta, neuroscience products including Botox Therapeutic and Vraylar, and the aesthetics business acquired with Allergan. Headquartered in North Chicago and listed on the New York Stock Exchange, it is one of the largest pharmaceutical companies by revenue.

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

IQA technicians are responsible for all the activities detailed in IQA procedures. Below is a list of typical activities that all IQA technicians are responsible for; this list is not exhaustive, and it is expected that the technicians are progressive with the company and as new systems come in and are replaced with others, this list will change. In all cases, adequate training will take place before the IQA technician is requested to carry out the activity.

Key /Accountabilities

  • Release of Production and Packaging components across all BU's

  • Issue components to Packaging / Production

  • Complete In -process checks in the BU's.

  • Visual Inspection/ PA testing of Finished Product

  • Complete complaints investigation for complaints department on GTW

  • Participate in QA and EHS Gemba’s

  • Paperwork review, logbook review

  • Audit preparation and participation

  • Proven track record in a quality discipline in the Pharma/Medical Device environment.

  • Third level Science qualification advantageous but not critical.

  • Keen attention to detail and ability to multitask.

  • Good communication skills and team player.

  • Ability to use sound judgment to make effective decisions within appropriate timeframes.

  • Proven to be self-directed, self-motivated and ability to prioritize competing priorities.

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.html

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