Quality Professional

Quality Professional page is loaded Quality Professionallocations: Ireland - Longfordtime type: Full timeposted on: Posted Todayjob requisition id: JOB DESCRIPTION: About Abbott Abbott is a global healthcare leader committed to helping people live healthier, fuller lives at every stage. Our portfolio spans diagnostics, medical devices, nutritionals, and branded generic medicines, serving patients in more than 160 countries with a workforce of over 115,000 employees worldwide.In Ireland, Abbott employs over 6,000 people across ten sites, including six manufacturing facilities in Clonmel, Cootehill, Donegal, Longford, and Sligo, as well as commercial and shared services operations in Dublin and Galway. Abbott has been operating in Ireland since 1946. The Role - Quality Professional We are seeking a Quality Professional to support the delivery of compliant, high-quality products, processes, and services. This role plays a key part in maintaining quality standards, driving continuous improvement, and ensuring compliance within a regulated environment. Key Responsibilities Quality Systems & Compliance Ensure adherence to quality standards, policies, and regulatory requirements Identify and escalate non-compliance issues in a timely manner Support ongoing compliance with Abbott's Quality Management System and Quality Policy Operational Quality Support Review and approve documentation and process orders Perform inspections of incoming materials/components, where applicable Ensure all activities and documentation meet compliance standards Risk Management & Problem Solving Apply risk management principles (e.g., FMEA) to support quality outcomes Investigate quality issues and complaints, recommending effective solutions Exercise sound judgement in resolving issues of moderate complexity Project & Process Improvement Support quality-related projects and cross-functional initiatives Identify opportunities for process improvements and support change implementation Contribute to validation activities, design controls, and change control processes Collaboration & Stakeholder Engagement Work cross-functionally with engineering, operations, and suppliers Provide guidance and support to technicians and junior team members Participate in audits, reviews, and business initiatives Education & Experience Third-level qualification (or equivalent experience) in Life Sciences, Engineering, or a related discipline Minimum of 3 years' experience in a quality or regulated environment (less may be considered with advanced qualifications) Strong understanding of quality systems and regulatory requirements Demonstrated ability to support business objectives through quality excellence and continuous improvementThis is an excellent opportunity to work in a dynamic, regulated manufacturing environment , contributing to products that positively impact patients' lives worldwide while developing your career in quality and operational excellence. 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. Connect with us at or , on LinkedIn at , on Facebook at and on Twitter . The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted. JOB FAMILY: Operations Quality DIVISION: CRLB Core Lab LOCATION: Ireland > Longford : Lisnamuck ADDITIONAL LOCATIONS: WORK SHIFT: Ie - Lfdflsg2 (Ireland) TRAVEL: No MEDICAL SURVEILLANCE: Yes SIGNIFICANT WORK ACTIVITIES: Not Applicable