At Abbott, you will play a crucial role to help people live more fully at all stages of their lives. Abbott is a global healthcare leader, and our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional products and branded generic medicines. Our 113,000 colleagues have a daily impact on the life of people in more than 160 countries.
Abbott Ireland
In Ireland, Abbott employs around 6,000 people across ten sites. We currently have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford, Sligo & Kilkenny and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.
Please note any offer of employment for this position is conditional upon the successful completion of a pre-employment medical examination, including drug and alcohol screening, conducted by a medical
practitioner designated by the Company
Diabetes Care Kilkenny
Our new manufacturing facility in Kilkenny, reflects the growing demand for Abbott's global Diabetes Care products. The facility will be a centre for world-class engineering, quality, medical device manufacturing, and other science-based professionals to produce life-changing technologies, including the FreeStyle Libre 3, a system that automatically delivers real-time, up-to-the-minute glucose readings, with the smallest and thinnest wearable glucose sensor that provides unsurpassed 14-day accuracy and optional glucose alarms directly to smartphones. This enables people with diabetes to live the best and fullest lives they can.
At Abbott in Kilkenny, you can shape your career as you help shape the future of healthcare.
This is how you can make a difference at Abbott:
As an Operations Quality Shift Lead, you will be responsible for general supervision of the manufacturing inspection and test functions at every stage of the manufacturing process. May supervise inspection and test activities of operators. Performs function failure testing as well as physical defects. This is a shift role on 4 cycles.
Key Responsibilities:
Oversees operational implementation of quality assurance strategies and regulations.
Completes the assessment of potential risks, ensures compliance, and gives recommendations to management.
Supervises team to ensure quality control aspects of the process are met (laboratories studies, clinical research, testing, operations, raw materials, production, finished product or services).
Facilitates audits and regulatory inspections.
Liaises with external vendors, contractors, or suppliers to ensure that their products or services meet the organisation's quality standards.
Lead a team of Operations Quality engineers.
Manage functional area’s compliance to site and divisional policies and procedures.
Lead the continuous improvement and effective maintenance of the QMS.
Subject Matter Expert in use of risk management tools to prioritise activities and justify the effort required.
Accountable for building and maintaining successful cross functional relationships with departments such as R&D, Technical, Engineering, Operations and Regulatory Affairs in order to achieve all project goals.
Manage teams Health and Safety within the working environment; highlight opportunities for improvement to EHS performance.
Act as Lead for the monitoring and compliance of the Quality Management System as it applies to site Operations:
Lead team in making Quality / Compliance decisions on product during processing, manufacturing, testing, monitoring, and packaging.
Lead audit readiness in functional area
Identify and lead projects to enhance and promote the effectiveness and efficiency of the quality system and product quality.
Champion a “right first time” approach to Quality Records by ensuring accountability for functional responsibilities.
Education and Experience
A minimum of a NFQ Level 7 Qualification in Science / Engineering or Manufacturing qualification
Minimum of 4 years’ experience in Manufacturing
Minimum 2 years’ experience people management
Yellow belt qualified desired
Strong communication and organisation skills
Strong problem solving
Experience with GMP/GDP
ISO13485 experience
What we Offer
Attractive compensation package that includes competitive pay, as well as benefits such as
Connect with us at www.abbott.com or https://www.ie.abbott/, on LinkedIn at www.linkedin.com/company/abbott-/, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.
Abbott is an equal opportunities employer.
