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 the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 113,000 colleagues serve people in more than 160 countries.
Abbott serves the Irish market with a diverse range of healthcare products including diagnostics, medical devices and nutritionals products. In Ireland, Abbott employs over 5,000 people across nine sites. We have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations and shared services in Dublin and Galway. We have been operating in Ireland since 1946.

Abbott Ireland Diagnostic Division Sligo
Abbott Diagnostic's is a global leader of in vitro diagnostics with approximately 70,000 institutional customers in more than 100 countries. Our diagnostic products offer a broad range of innovative instrument systems and tests for hospitals, reference labs, blood banks, physician offices and clinics.
Abbott’s diagnostic products offer customers automation, convenience, cost effectiveness and flexibility. Abbott has helped transform the practice of medical diagnosis from an art to a science, helping to create the modern diagnostics industry through the company's commitment to improving patient care and lowering overall costs. The history of Abbott Diagnostics is filled with examples of first-of-a-kind products and significant technological advancements.

The role of Associate Quality Professional Evening Shift will involve the following:

PURPOSE OF THE JOB:

General

• Budgets own time to carry out assigned duties that support business goals.
• Completes compliant documentation and provides solutions to local problems of low scope and complexity.
• Complete auditing and inspection of the Incoming material records and manufacturing documents
• Supports project work and acts as community member.

Quality System Compliance

• Ensures compliance to site level policies and procedures by promptly reporting non-compliance issues to the department manager or team leader.
• Risk Management - Applies basic Risk Management principles to work.
• Complaint Evaluation - Investigates standard complaints.
• Responsible for identifying Design Control / Documentation & Change Control
• Provides reasons and justifications in support of change.

EDUCATION & EXPERIENCE
Bachelor’s degree in Life Science, Engineering or closely related discipline, or an equivalent with a minimum of 12months experience in a similar role

HOURS OF WORK
Monday to Thursday 16:00-0:00
Friday 15:00-22:00