Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description AbbVie are currently seeking a Maintenance Planner to join our team in Cork . The successful candidate will facilitate the smooth and efficient operation of the engineering function by assisting our maintenance personnel to meet the demands of the business and production targets. You will support maintenance excellence by planning Maintenance activities using the company's computerised maintenance management system (CMMS). Roles And Responsibilities Monitor the operation of plant equipment and systems. Maintain a maintenance management system for tracking work orders, spare parts, and maintenance history of plant equipment. Track, analyse and improve key Maintenance Excellence Program (MEP) key performance indicators (KPI’s) parameters such as asset utilisation, maintenance cost, site maintenance compliance, schedule etc. Monitor sufficient inventories of spare parts and maintenance supplies, and initiate reordering when necessary. Ensure adherence to company safety standards, policies, and procedures. Proficient in the use of Computer Management Maintenance system (Maximo). Manage the purchasing for the department to reduce costs and add value. Manage the Engineering Change Control process to ensure there are no non-conformances relating to engineering change control. Build and maintain strong partnership with the EHS function to ensure both the safety of staff and contractors is seen as paramount on site. Participate constructively as a member of the dept, keeping everyone informed and proactively share knowledge and expertise within the team. Continuously review the maintenance schedules and liaise with the engineering team to update regularly. Optimise spares holding to effective levels by carrying out cycle counts and ordering and issuing parts when required. Supervision of Site stores personnel Purchasing and receiving of engineering parts and orders. Demonstrate commitment towards achieving department targets Perform internal audits on engineering systems, support external audits. Qualifications 5+ years experience in a similar Planning & Scheduling role Minimum Level 7 in Engineering, Process Plant Technology or Science degree. Fluent English - spoken and written Good communication skills and good problem-solving skills Microsoft Excel, Word and Outlook skills Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html #J-18808-Ljbffr
A leading biopharmaceutical company is seeking a Maintenance Planner to join their team in Cork. The successful candidate will optimize maintenance operations, facilitate smooth engineering functions, and support maintenance excellence through planning activities. A key focus will be on maintaining the management system and adhering to safety standards. Ideal candidates should have 5+ years of experience and a Level 7 degree in Engineering or related fields, while being proficient in relevant software and fluent in English. #J-18808-Ljbffr
Company Description AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Job Description The Senior Manufacturing Engineer plays a key role in supporting the Production Management Team, Project Managers, and Manufacturing Coordinators in driving day-to-day productivity within our manufacturing department. This position is responsible for leading planning initiatives, managing key performance indicators (KPIs), steering capital and efficiency projects, overseeing technical non‑conformance reports (NCRs), and administering SAP systems. The Senior Manufacturing Engineer will be instrumental in optimizing processes, improving yields, and fostering continuous improvement initiatives. Key Responsibilities Develop and implement daily, weekly, monthly, and project work timetables for the Manufacturing Coordinator team, ensuring alignment with Production Manager deadlines. Conduct Kronos administration and monthly one‑on‑ones for all direct reports into the Senior Manufacturing Coordinator. Take ownership of closing NCRs, Change Plans, and CAPAs within required timeframes, leading technical NCRs to successful cross‑functional resolution. Collaborate with the supply chain team to plan manufacturing schedules. Serve as SAP local key user, responsible for system administration and optimization. Monitor and manage production stock levels using SAP. Oversee system changes for manufacturing products, including generating Bills of Materials (BOMs), batch record updates, and product amendments. Identify and implement initiatives to improve production and business process efficiencies, focusing on increased yields, reduced throughput times, improved flows, cost savings, waste elimination, and enhanced safety. Manage production deviation systems, analyzing trends and executing corrective/preventive actions. Drive Lean Six Sigma and 5S programs within the Production Department. Ensure quality compliance in all work processes. Health & Safety The Senior Manufacturing Engineer shares responsibility for upholding Environmental, Health, Safety & Energy (EHS&E) standards, fostering a culture of compliance and proactive safety improvement. You will contribute to maintaining high EHS&E standards, communicate the Safety Statement & Standards Manual, and support AbbVie’s programs in alignment with applicable regulatory standards (ISO 14001, OHSAS 18001, ISO 50001, and relevant workplace acts and regulations). Qualifications Bachelor’s degree (or equivalent 3rd level qualification) in a relevant Science, engineering or technical discipline. 3-4 years of experience in a front‑line role (supervisor, coordinator, specialist, etc.) within a production manufacturing environment (preferably Oral Solid Dosage). Proven experience in identifying and delivering process/business efficiency improvement projects. Established experience in a continuous improvement environment, with knowledge of Lean Manufacturing and Six Sigma principles. Expert working knowledge of SAP. Excellent written and verbal communication skills, with demonstrated teamwork and presentation abilities. Fluency in English is required. Additional Information Why Join Us? At AbbVie, you will be part of a team dedicated to advancing productivity, quality, and safety in manufacturing. We foster a collaborative environment focused on professional growth, innovation, and operational excellence. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html #J-18808-Ljbffr
A global biopharmaceutical company in Cork, Ireland, seeks a Senior Manufacturing Engineer to enhance productivity and quality in manufacturing. This role emphasizes process optimization, leading initiatives for efficiency improvement, and requires expertise in SAP and Lean Manufacturing principles. The ideal candidate should have a degree in a relevant discipline and 3-4 years of relevant experience. Join a team committed to innovation and operational excellence. #J-18808-Ljbffr
Join to apply for the Automation Team Lead role at AbbVie Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description We have an exciting new opportunity for an Automation Team Lead, This reports to the Associate Director of Automation and will be pivotal in supporting our transition to the Factory of the Future, utilising control systems such as Siemens, Rockwell, and Wonderware. The successful candidate will manage a team of 8-10 Automation Engineers, oversee several automation projects, and provide ongoing operations support for AbbVie's Eye Care Business Unit. This position offers potential for career advancement in management while contributing to innovative automation solutions. Roles And Responsibilities Lead, supervise and manage a team of 8-10 Automation Engineers across the BUs and ensure uptime and efficiency Define team schedules, rota for off-shift/on-call support, and oversee training and development. Serve as primary point of contact onsite for Automation related issues Assign key SMEs within the group to best support the issues in manufacturing and packaging Work with team to develop optimum solutions to process automation issues Escalate complex issues to the Associate Director of Automation to get additional support from PLC and SCADA SMEs within the group Responsible for delivering support to the business and achieving system metrics. Evaluate process improvements and initiate projects to improve reliability, improvement processes or eliminate waste Manage automation improvement projects, track milestones, and drive results to meet schedules. Manage automation vendors and contractors including system support contracts and external access arrangements. Support Capital project requests for automation support, if required. Support cost savings initiatives onsite and within the engineering team Support any safety or quality initiatives that required automation support Work closely with the Business Technology Services group Ensure systems comply with cGMP/regulatory requirements and SOPs Support DI (Data Integrity) issues that arise within the Business Support automation related change controls. Support long term plans for control system maintenance and improvements. Direct project execution by assigning tasks, tracking project schedules, identifying risks, and developing and executing contingency plans. Communicate project status by preparing standard status reports, and by participating in departmental and customer project status update meetings. Resolve project/system issues by working with team members, project customers, and others as appropriate. Manage and approve associated documentation and specifications. Supports the execution of control systems project activities as per site business needs and to meet clearly stated objectives. Act as a key contact for automation-related audits and reviews. Qualifications Degree in a relevant subject area such as Mechatronics / Engineering Strong knowledge of manufacturing and control systems is essential Minimum of 5 years’ experience in Batch processing operations in an FDA/ HPRA regulated industry. 3 years’ experience in configuring control systems in a batch manufacturing environment 1 -2 years’ experience in a people management/supervisory role would be an advantage. A strong knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry. Experience of operating in a team environment with active participation in proactive improvement programs is required. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. #J-18808-Ljbffr
Chemistry Supervisor, Laboratory Quality Control Join to apply for the Chemistry Supervisor, Laboratory Quality Control role at AbbVie Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. Job Description We are now hiring a QC Analytical Lab Supervisor to join our team in Abbvie Ballytivnan, Sligo . You will lead the QC Analytical team and ensure the continued success of the team. Ensure that technical and systems excellence is maintained in the laboratory by ensuring own skills are maintained, by coaching and training analysts to ensure right first-time behavior and by implementing improved working practices in terms of efficiency, compliance and Right First Time. A snapshot of your key responsibilities: Supervise Daily Laboratory operations, ensuring personnel execute their responsibilities in strict accordance with relevant regulatory guidelines. Ensure Laboratory Documentation and Computerized Systems (LIMS, Empower, LabX) compliance with Data Integrity policies and regulatory requirements. Supervise the QC Analytical laboratory operations and ensure compliance with regulations including EU Annex 1, ISO, WHO, FDA Guidelines for Aseptic Processing, among others. Resolving analytical OOS issues as they arise in a timely manner both through practical work and through solTRAQs/OneTrack systems. Review of results from Clean & Utilities program (WFI/RO/CS water testing), Product Testing (In process and Final product as required) and Analytical Lab (pH, TOC, Conductivity, Osmolality, Density, HPLC, Raman, etc.) activities, results and raw data on time, accurately and legibly. Participate actively in Laboratory Investigations Reports (LIRs), Invalid results investigation review, approval and creation of effective CAPAs. Ensuring 6S excellence is maintained across the Laboratory. Instilling a quality culture of Zero, Believe it, Achieve it amongst the QC laboratory team. Lead and contribute to project initiatives to improve laboratory operations and efficiency as assigned by the QC Lab Manager. Work with a cross functional team, Supervisors, Quality Manager and Laboratory Manager to ensure compliance with Quality Management System. Support the training and mentoring of laboratory personnel and contribute to training program development. Operates in an environment which is essentially self-managed but with supervision through the Laboratory Manager. Provides supervision to direct reports and be responsible for setting annual goals, completing reviews, growth plans and performance management of the team. Qualifications BS in science or equivalent (Chemistry, Microbiology, or Biology preferred). 2-5 years of laboratory experience. 2-5 years of supervisory experience. Demonstrated skills to deal effectively with members of the department and the areas serviced by the laboratory. Problem solving skills are required. Must be able to interpret impact of laboratory data for appropriate and effective actions. Must be able to identify problem areas requiring development, maintenance, production, engineering, accounting, or planning with assistance from more senior staff. Must also be able to identify, communicate, and follow-through to completion and assist in the development of necessary corrective action plans to resolve the problem with supervision. Additional Information 3rd Level Qualification in a Science Discipline, preferably Analytical related. Job Technical Skills Minimum 4 years experience in the pharmaceutical industry. Proven track record in an analytical role. Must be expert in HPLC, Raman, pH, Osmolality, Conductivity, among others. Experience with HPLC, Raman and Analytical methods (pH, TOC, Osmolality, Density, among others) preferred. Experience and good knowledge of SampleManager and Empower systems. Involvement in product transfers / method transfer, method development experience preferred. Good knowledge and understanding of Data Integrity from Laboratory perspective. Preferable knowledge in ADC (Antibody-Drug Conjugate), mAb (Monoclonal Antibodies) and Aseptic process production. Business Skills Excellent communication, organization, time-management and teamwork skills. Requires a high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures. Requires total commitment to quality and maintaining a high standard of work at all times. Demonstrate ability to work on one’s own initiative. Strong Problem-solving skills. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. #J-18808-Ljbffr
Overview Quality Assurance Manager role at AbbVie. This role is responsible for ensuring that all products manufactured at AbbVie meet GMP, end-user, Regulatory Authority, and AbbVie standards. The QA Manager will oversee team performance, compliance activities, audits/inspections, and serve as a critical partner to operational functions to maintain and improve quality across the site. Responsibilities Ensure products manufactured at AbbVie meet requirements of end users, Regulatory Authorities, and AbbVie. Lead and manage the Quality Assurance team, providing guidance and support on quality and compliance matters. Act as a site contact for regulatory and customer audits/inspections (FDA, HPRA, etc.) and prepare site teams for successful outcomes. Manage CAPA (Corrective and Preventive Action) implementation, and follow-up activities. Collaborate cross-functionally to resolve quality issues, improve processes, and ensure continuous compliance with cGMP and other relevant regulations. Promote department goals by attracting, developing, and retaining capable QA staff. Contribute to talent management and professional development of QA personnel. Develop, review, and approve QA documentation as related to general QA activities. Provide oversight of batch record review, deviation investigations, change controls, and product release decisions. Support quality meetings and key quality metrics and trends. Communicate effectively with internal and external stakeholders, including the AbbVie Quality and Compliance Group and regulatory bodies. Serve as a designee for the Biologics Quality Director as required. Qualifications Bachelor's degree in science, Quality, Engineering, or related field (Master’s preferred) Minimum of 8 years’ experience in the healthcare, pharmaceutical, or biopharmaceutical industry At least 3 years’ supervisory/people management experience Demonstrated experience with audits and/or inspections (FDA, HPRA, etc.) High level of expertise in day-to-day quality and compliance decision-making In-depth knowledge of GMP requirements and regulatory frameworks Strong attention to detail and commitment to compliance and quality standards Ability to facilitate quality decision-making while maintaining a strong patient focus and upholding AbbVie’s reputation Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html #J-18808-Ljbffr
Join to apply for the Automation Engineer role at AbbVie Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow AbbVie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description We are currently looking for an Automation Engineer to join our Biologics site in Sligo Ballytivnan. The Automation Engineer plays a critical role within our Engineering department, providing technical support and program management across all manufacturing operations and New Product Introductions (NPIs) at the site. This position offers technical leadership for all control system activities in our pharmaceutical manufacturing facilities, ensuring seamless operations and continuous improvement in a regulated environment. Responsibilities Lead and manage all automation and control system initiatives, including validation and integration with MES/ERP/Data Historian systems. Provide daily technical support, troubleshooting, optimization, and documentation control for control system-related issues. Oversee life cycle management of on‑site control systems, ensuring compliance with AbbVie’s SLC and relevant regulatory requirements. Drive the execution of continuous improvement projects, closely collaborating with process engineers and other departments. Support plant start‑ups, new product introductions, and ensure systems meet cGMP and HPRA/FDA regulations. Develop and maintain relationships with vendors and participate in vendor qualification and documentation review. Foster a culture of safety, compliance, and quality through adherence to EHS and regulatory standards. Qualifications Essential: NFQ Level 8 Honors Bachelor’s Degree or Higher Diploma in a relevant technical discipline. Minimum 3+ years in automation engineering, with PLC/HMI/SCADA software development experience in GMP pharmaceutical environments. Strong knowledge of 21 CFR Part 11 requirements for automated systems. Experience with plant start‑ups and/or new product introductions to pharmaceutical facilities. Advantageous: Experience with control system validation, auditing, and internal inspection. Exceptional problem‑solving skills, innovative thinking, high attention to detail, and strong commitment to quality and results. Excellent verbal and written communication, strong interpersonal, and leadership skills. Ability to work autonomously, show initiative, and collaborate across multiple departments. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only – to learn more, visit equal employment opportunity employer . US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more. Seniority Level Entry level Employment Type Full‑time Job Function Engineering and Information Technology Industries Pharmaceutical Manufacturing and Biotechnology Research #J-18808-Ljbffr
A leading global biopharmaceutical company in Cork, Ireland, is seeking a Senior Project Manager to oversee large-scale strategic projects critical for innovation in drug manufacturing. The ideal candidate will possess a BS in Engineering and a minimum of 10 years in an Engineering Leadership role with expertise in aseptic and sterile manufacturing technologies. Proven leadership and communication skills are essential, along with strong financial acumen to monitor project performance and manage costs effectively. This position requires occasional travel to various project sites. #J-18808-Ljbffr
Senior Project Manager, Strategic Projects AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Purpose The Project Manager will lead strategic and large-value capital projects that are critical to delivering the ability of our manufacturing network to deliver innovative medicines to patients. The incumbent will be responsible to achieve all project objectives including EHS, Scope, Schedule, Cost, Quality and Compliance while driving top‑tier performance of consultants, architecture/engineering firms, construction contractors and managers. This role requires close cross‑functional collaboration with other functions such as ME&C and Quality during all phases of the development of the strategic project. Responsibilities Single point responsibility to ensure that all project objectives are achieved. Implement all applicable EHS and Engineering Policies and procedures and ensure compliance with them. Drive EHS performance of all project activities including construction safety. Ensure that project related work does not impact existing facilities or operations. Drive implementation of best‑in‑class design within the scope boundaries in consultation with key operations stakeholders. Manage and be responsible for all phases of project execution. Monitor and manage the risks associated with the project ensuring appropriate plans are in place to address and mitigate risks as they arise. Escalate risks to steering committee, when required. Demonstrate exceptional financial acumen and control over costs including ability to plan and project capital and expense spend over the project duration. Provide LBE and estimates to complete on a monthly basis. Demonstrate agility to push the envelope of project execution to drive efficiencies of resources and costs including implementation of value engineering, alternate options and scenarios, fallback strategies. Lead, in cooperation with Procurement, strategic sourcing needs for the project including assisting with contract negotiations, managing scope and schedule creep and dispute resolution. Monitor and measure project progress and performance through an established set of KPIs. Proactively take steps required to mitigate any impact on schedule, cost, quality and EHS. Foster an environment of innovation and exchange of ideas. Keenly learn novel concepts and integrate in the project. Communicate effectively with all levels in the organization. Present project performance to steering committees, senior leadership, regulators and government agencies. Qualifications BS, Engineering or equivalent technical degree. Minimum of 10 years of experience as an Engineering Leader/Projects/Operations Leader across multiple drug product operations. In‑depth technical and operational expertise in manufacturing technologies related to aseptic and sterile manufacturing. Expertise in multi‑format drug product filling lines and lyophilizer, small volume cytotoxic product filling will be an advantage. Proven inclusive management and leadership capabilities of diverse, cross‑functional teams. Listens to and understands others’ points of view and articulates tactfully and respectfully one’s own perspective orally, in writing, and in presentations. Able to communicate with senior leadership, regulators, and government agencies. Excellent negotiation skills combined with financial acumen and experience of leading projects with a cross‑functional team. Able to lead change and deliver results across a matrix organization. Business acumen and direct financial planning/budgeting experience required including P&L responsibility. Ability to mentor and develop next generation of leaders. Position will be site‑based but travel to other project sites and design reviews/workshops will be required. Additional Information Closing Date for applications: January 9th 2026. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer / Veterans / Disabled. US & Puerto Rico only – for more information, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html. US & Puerto Rico applicants seeking a reasonable accommodation can learn more at https://www.abbvie.com/join-us/reasonable-accommodations.html. #J-18808-Ljbffr
