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About Abbott
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans diagnostics, medical devices, nutritionals, and branded generic medicines. With over 113,000 colleagues, we serve people in more than 160 countries.
In Ireland, Abbott employs around 6,000 people across ten sites, including manufacturing facilities in Clonmel, Cootehill, Donegal, Longford, Kilkenny, and Sligo, along with support operations in Dublin and Galway. Abbott has been operating in Ireland since 1946.
Job Purpose
Responsible for reviewing all Quality Records (QRs), providing leadership and direction for QR initiation and root cause analysis, and ensuring site Quality CAPA Metrics are recorded and reported.
Major Responsibilities
1. Conduct weekly or more frequent CAPA meetings to track timelines and quality of QRs and actions.
2. Lead and support the Corrective and Preventive Action System for all plant personnel.
3. Ensure site Quality CAPA metrics are recorded, verified, and reported monthly.
4. Provide training on CAPA requirements to site SMEs and staff.
5. Review site QRs for compliance with Rubric and policy requirements.
6. Compile CAPA information for management review and area reports.
7. Guide management on handling manufacturing events, containment, and sampling.
8. Complete Global CAPA reviews and support issue escalation post-QR approval.
9. Support the QA CAPA IT System (ABTRAQ), including system development and user support.
10. Collaborate with other CAPA Specialists in global community meetings.
11. Participate in Food Safety Team meetings, internal audits, and walkdowns.
Qualifications
Diploma/Degree in science or engineering with at least three years of manufacturing experience in a regulated quality assurance environment.
Additional Information
Connect with us at Abbott's website or social media platforms for more information.
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