Quality Control Technician
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Westport, MO
- Operations
- On-Site
- Full-time
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.
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Where We Work
Role is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.