Technician, Quality
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Sligo, ie
- 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.
What you do, is what we need. Making a difference begins here. And takes all of us.
Welcome to AbbVie!
We are a global, research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceutical leader. Redefining what is possible is our business and our passion. Our goal is to help patients live healthier lives and we are proud to be a Great Place to Work.
We are looking for a Quality Technician to join our team in Ballytivnan, Sligo. This is a Permanent position. The position reports directly to the Quality lead.
This role is a permanent evening shift position.
What you will do:
- Work as a member of the Quality Team to ensure that Quality goals and objectives are achieved.
- Ensure that all actions comply with current good manufacturing practices.
- Operate within the QC/ IQA and Metrology Areas, as required
- Complete incoming product testing per the relevant approved specifications and procedures.
- Complete in-process and final release product testing per the relevant approved specifications and procedures.
- Ensure Management is kept informed of all Quality Events or potential Quality Events Related to the product or process.
- Ensure all Quality System documentation is thorough, complete, and compliant.
- Audit the quality system with other personnel where required.
- Support Change Management Process including Product and Quality System document review and updates.
- Generate and Providing metrics for inclusion in the management review, monthly reports and overall Quality performance.
- Ensure compliance to training requirements is maintained.
- Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems at the site.
- Generate batch records for as required in support of manufacturing process orders.
- Complete disposition decisions for incoming material
What you will need:
- 2 years’ experience in a medical device/ manufacturing background in a similar role
- 3rd level qualification
- Ability to work on own initiative
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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Pay Range: $
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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.