A global pharmaceutical company based in Dublin is seeking an Associate Director for Supply Chain Brand management. This pivotal role requires extensive experience in managing complex operations that impact billion-dollar sales across various portfolios. The ideal candidate will collaborate with multiple functions, ensuring seamless integration of developmental products into strategic planning. Strong strategic thinking and excellent communication skills are essential. Join us for a chance to make a significant impact on patients' lives worldwide. #J-18808-Ljbffr
About AbbVie 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Associate Director, Supply Chain Brand, will have responsibility for working with one of our brands initially, with scope increasing to cover other portfolios over time. Reporting to the Senior Director, this is an exciting time to join AbbVie as we continue to produce medicines that positively impact patients lives all around the world. Main duties Coordinate complex Supply Chain and Operations Teams to align with business goals, ensuring strategic contributions and compliance. Lead complex operations impacting billion-dollar sales, interface with stakeholders, manage strategies, risk management, and lead negotiations. Primary interface with a wide variety of functions in both Ops and Commercial. Ensures alignment on brand/product forecasts, as well as key cross functional project initiatives. (Commercial Directors, VPs, and SVPs) Direct and present S&OP topics at the executive level across functions, driving synergy between demand and supply planning, with comprehensive oversight of operational performance via KPIs and other targets. Develop and drive strategies to ensure long term continuity of supply. Oversee and align the financial planning cycle, including LRP and annual Plan, while managing inventory and ensuring synchronization of strategic goals with financial planning across functions. Lead lifecycle management with a strategic view, ensuring changes align with business goals and collaborating with cross-functional teams for smooth transitions. Create change plans and supply chain assessments in executing lifecycle programs. Interact with the Industrialization team to ensure strategic integration of developmental products into brand planning, aligning timelines and resource allocation with operational strategies. Direct alignment between brand and Clinical Drug Supply Management to meet strategic trial needs, ensuring synchronization of supply chain and clinical demand planning. Oversee interaction with PPDST and Asset Strategy Teams ensuring collaborative strategy development, aligning product roadmaps and brand positioning with asset strategies. Direct leadership which through mentoring and development of emerging talent, fosters a culture of collaboration and accountability within teams. Qualifications Bachelor’s degree in Engineering or similar area (Masters preferred including MBA) Extensive experience in Supply Chain and lifecycle management. High-level strategic thinking and excellent communication skills with the ability to shape discussions and influence at executive level. Large-scale change management experience and knowledge. Operations experience preferred; in pharma / regulated life sciences business. Excellent knowledge in data analytics and comfortable with telling a story through data Ability to filter and identify the business-critical aspects of a problem (separate the minor issues from the major issues) 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 pharmaceutical company in Westport seeks an experienced Associate Director of Automation to lead the Automation and Operational Technology team. This role involves driving compliance, optimizing processes, and managing a skilled team. The ideal candidate will possess a relevant degree and 8–10 years in a regulated environment, demonstrating leadership in automation projects. Competitive salary and benefits offered. #J-18808-Ljbffr
A leading biopharmaceutical company in Sligo is seeking a Senior Manufacturing Compliance Specialist for their Quality Assurance operations. The ideal candidate will ensure product excellence through quality compliance and provide oversight in a collaborative manufacturing environment. Responsibilities include guiding product standards, leading investigations, mentoring team members, and ensuring compliance with regulatory standards. Applicants should have at least a third-level degree in science, quality, or engineering, along with a minimum of three years’ experience in GMP settings. #J-18808-Ljbffr
About AbbVie 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 As a Reliability Engineer at our North Dublin Site , you will play a key role in supporting the Maintenance Excellence Program (MEP) through advanced reliability engineering methods. You will be a technical problem‑solver and champion for quality and operational improvements. Lead the MEP Program by delivering criteria set out in Reliability Engineering minimum requirements and driving metric attainment. Owner of Site CMMS (Maximo) ensuring best in class practices, procedures and compliance are in place and adhered to. Drive best in class maintenance practices, managing governing procedures and compliance across the Site. Conduct reliability analyses including RCM, FMEA, and RCA on critical assets. Review and optimize preventive maintenance programs and conduct effectiveness assessments. Monitor operations of plant equipment to identify/prevent emerging failures. Analyze maintenance work orders and equipment failure history; develop solutions to recurring issues. Manage predictive maintenance and mechanical integrity programs. Review maintenance and installation plans for new equipment and provide reliability specifications. Drive continuous improvement to minimize equipment and utility risks. Support optimization and improvement of critical assets. Engage with global engineering and participate in engineering forums. Ensure compliance with procedures, policies, and regulatory standards (GMP, HPRA/FDA). Collaborate with cross‑functional teams on projects and improvement initiatives. Champion EHS practices and supports a culture of safety excellence. Qualifications Third‑level qualification in Engineering. 5 years’ engineering experience ideally gained in a cGMP environment. Proficiency in Computerised Management Maintenance Systems (Maximo an advantage). Strong computer literacy with the ability to analyse data. Reliability engineering and continuous improvement experience. Demonstrated problem‑solving and innovative thinking skills. High attention to detail and commitment to right‑first‑time ethos. 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
About AbbVie 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 atwww.abbvie.com . As a Reliability Engineer at our North Dublin Site , you will play a key role in supporting the Maintenance Excellence Program (MEP) through advanced reliability engineering methods. You will be a technical problem-solver and champion for quality and operational improvements. Lead the MEP Program by delivering criteria set out in Reliability Engineering minimum requirements and driving metric attainment. Owner of Site CMMS (Maximo) ensuring best in class practices, procedures and compliance are in place and adhered to. Drive best in class maintenance practices, managing governing procedures and compliance across the Site. Conduct reliability analyses including RCM, FMEA, and RCA on critical assets. Review and optimize Preventive Maintenance programs and conduct effectiveness assessments. Monitor operations of plant equipment to identify/prevent emerging failures. Analyze maintenance work orders and equipment failure history; develop solutions to recurring issues. Manage Predictive Maintenance and Mechanical Integrity Programs. Review maintenance and installation plans for new equipment and provide reliability specifications. Drive continuous improvement to minimize equipment and utility risks. Support optimization and improvement of critical assets. Engage with Global Engineering and participate in engineering forums. Ensure compliance with procedures, policies, and regulatory standards (GMP, HPRA/FDA). Collaborate with cross-functional teams on projects and improvement initiatives. Champion EHS practices and supports a culture of safety excellence. Qualifications Third-level qualification in Engineering. 5 years’engineering experience ideally gained in a cGMP environment. Proficiency in Computerised Management Maintenance Systems (Maximo an advantage). Strong computer literacy with the ability to analyse data. Reliability engineering and continuous improvement experience. Demonstrated problem-solving and innovative thinking skills. High attention to detail and commitment to right-first-time ethos. 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 applicants seeking a reasonable accommodation, click here to learn more: #J-18808-Ljbffr
A leading biopharmaceutical company in Westport is seeking a skilled NPI Launch Site lead to oversee New Product Introduction Programs. This role involves managing a team and providing technical support for product transfers in compliance with regulatory standards. The ideal candidate has a Master's degree in a relevant Science area and extensive experience in Process Engineering. Strong leadership and communication skills are essential for collaboration across departments and ensuring product quality and efficiency. #J-18808-Ljbffr
Overview 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 looking for a Senior Process Safety Engineer to join our team in Abbvie, Manorhamilton Road, Sligo . The Senior Process Safety Engineer will be responsible for developing, implementing, managing systems and procedures to prevent major accidents or incidents. You will also be responsible for maintaining and enhancing current systems and ensuring a safe and fit for purpose Process Safety environment. Emergency response and business continuity will also be key areas of responsibility. Responsibilities Lead the introduction of new products to the site from a process safety perspective. Safe Process Design and Review. Evaluate and design safety systems, including emergency shutdown systems, pressure relief devices (PRDs), fire protection, and explosion prevention systems. Develop and further improve Emergency response and preparedness capabilities. Chair and document process and equipment HAZOP assessments and other process safety related risk assessments and drive follow up actions. Complete Pre-Start Up Safety Reviews (PSSR) in line with relevant Abbvie Technical Standards. Be responsible for process safety elements associated with running product campaign(s) on plant and ensuring that all processes are managed effectively. Propose, develop, and implement improvements and modifications from a process safety perspective to process areas and equipment to improve operations. Ensure compliance with relevant legal, site, corporate, and industrial standards. Interact with the Management of Change (MOC) and change control system and approve from an EHS perspective. Support safety investigations throughout the site and troubleshoot related process safety issues. Lead or participate in root cause analysis (RCA) for major incidents. Review and approve process safety-related documentation, for example, Process Hazard Analysis and Capital Project Lifecycle system requirements. Provide relevant training and mentor less experienced engineers, supporting their development in process safety. Conduct safety audits and continuously improve the Site safety management systems. Engage with internal and external stakeholders, including regulatory authorities and third-party auditors, to drive compliance and continuous improvement. Utilize digital risk management tools, process safety modeling software, or data analytics for risk assessment and improvement of process safety practices. Integrate process safety with sustainability and environmental initiatives, such as safe handling of hazardous waste and reducing process-related emissions. Interact with Abbvie Global Process Safety SMEs and maintain Process Safety KPIs and Metrics. Participate in relevant professional networks and support continuous professional development related to process safety. Qualifications A bachelor's degree in Chemical, Process, or Mechanical Engineering. 5+ years of relevant experience in a process-related industry (e.g., pharmaceutical, chemical, petrochemical). Strong knowledge of process safety management (PSM) principles, risk assessment methodologies (PHA, HAZOP, LOPA, etc.), ATEX and COMAH principles (related to explosive atmospheres), and relevant industry standards (e.g., IEC 61508/61511 for functional safety). Excellent analytical and problem-solving skills, strong written and verbal communication skills, attention to detail, and the ability to work effectively within cross-functional teams. Chartered Engineer status or TUV Rheinland/equivalent certification in Functional Safety would be an advantage. Experience with process safety digital tools and modeling software is desirable. Proven ability to collaborate with diverse teams and stakeholders. 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
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 Biologics Ballytivnan seeks a Senior Manufacturing Compliance Specialist to strengthen our Quality Assurance operations. In this role, you'll help ensure product excellence through quality compliance, incident resolution, and floor-level support within a collaborative manufacturing environment. Responsibilities Ensure all products and process simulations meet standards for market/investigational use. Provide quality guidance and compliance oversight throughout manufacturing. Lead or support investigations related to non-compliance in product or processes. Mentor, train, and provide support to shift team members. Audit batch documentation, review logs, and process SOPs. Support and execute line clearance, raw material checks, and stability program activities. Manage and maintain finished product status, labeling, and quality logs. Conduct daily manufacturing area walkarounds and seek process improvements. Support quality aspects of MVI, AQL, and NPI process/material handovers. Maintain compliance with cGMP, HPRA/FDA, EHS, and AbbVie standards. Qualifications Third-level degree in science, quality, or engineering. Minimum 3 years’ experience in a GMP quality/operations setting (biologics preferred). Strong experience in aseptic processing and advanced knowledge of regulatory requirements. Excellent written/verbal communication and interpersonal skills. Experience as a trainer preferred. Demonstrated commitment to quality, problem-solving, and continuous improvement. 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
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 Reporting to the Planning Program Director. Your role at AbbVie You will be employed on a 2 year contract initially with the ambition to move to perm. Highlighted Responsibilities Develop change management plans based on the AbbVie Change Management and the Ways We Work approach. Provide strategic direction and methodology for the Communication and Change Management approach for global Supply Chain Planning organization. Promote the function or department culture through communication and programs. Own and deliver against a comprehensive communication plan for internal communications; ensure messages are being delivered to the right audience at the right time, in a consistent and engaging format. Leverage change management methodology and apply as appropriate for the business environment, focusing on execution and impact. Support, Build and Implement training programs. Lead process improvement and optimization initiatives for the organization. Qualifications Bachelor’s degree in organizational development, Communications, Public Relations, English or related field required. Understanding of change principles and methodologies with the ability to define a flexible, unique approach based on the business team and working environment. Experience leading and executing against a comprehensive communications plan. Highly developed communication skills with expertise in producing organization-wide communications and development of a communication strategy. Experience with project management approaches, tools, and phases of the project lifecycle. Experience and knowledge of Supply Chain. AbbVie has been at the top of the global 'Best Workplaces' list in the Netherlands, Europe and worldwide for several years in a row. We are proud of this! This recognition by Great Place to Work reflects employee experiences of trust, innovation, company values and leadership, across Europe. It is an acknowledgement of being a fulfilling workplace, a recognition of our culture and the result of the ways we work together. 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
