Have you ever wanted to make a difference? 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 115,000 colleagues have a daily impact on the life of people in more than 160 countries.We currently have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo 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.Abbott Vascular Clonmel is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education.
Our broad line of vascular devices manufactured in Clonmel includes vessel closure, endovascular and coronary technologies designed to treat heart attack, stroke, critical limb ischemia and other serious vascular conditions.
Abbott Vascular Clonmel is the largest Abbott Manufacturing facility in Ireland focusing on both manufacturing and research and development of next generation vascular products.
Provides support to the manufacturing organisation to facilitate efficient operations within the production area, to optimise existing processes, and to ensure that production goals are met.
Monitors performance of equipment, machines and tools and corrects equipment problems or process parameters that produce non-conforming products, low yields or product quality issues.
Interfaces with research and development organisations to integrate new products or processes into the existing manufacturing area.Implements a staffing plan by identifying resources requirements, and liaise with next level management on writing justifications for additional personnel, obtaining approval for changes, and coordinating the selection process with human resources.
Develops direct reports by securing appropriate training, assigning progressively challenging tasks, applying progressive disciplinary action as appropriate in conjunction with next level management and conducting formal written and verbal performance reviews.
Monitors daily work operations and provides direction and guidance to experienced exempt employees, or skilled nonexempt staff to achieve unit or project goals.
Interacts with internal and external customers, by meeting regularly, responding to requests and explaining procedures.Monitors compliance with company policies and procedures for example with Food and Drug Administration (FDA), British Standards Institution (BSI), relevant employment law etc.
Contributes to the development and monitoring of area budget through regular analysis of cost and spending in conjunction with next level management.
Participates in validation activity. Role may vary between providing input to owning activities such as protocol/report writing and managing execution of validation activities.