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 is seeking a dynamic QA Systems Digital Lead to spearhead our QC Digital and Lab of the Future programs in Manorhamilton Road, Sligo. This role is crucial in aligning digital initiatives with QA objectives and enhancing lab automation and compliance efforts. As a pivotal member of our team, you will manage key projects, ensure systems stay updated and compliant, and drive continuous improvement in our quality assurance processes. Key Responsibilities: Oversee the QA IT group's activities, including management of LIMS, SAP, Empower, and lab connectivity. Lead digital laboratory initiatives such as Lean Digital Lab, Lab of the Future, and Smart QC. Optimize quality control systems for greater efficiency and ensure data integrity across all systems. Implement and manage site-specific QC digital programs in line with organizational goals. Provide leadership in QC laboratory technology, collaborating with BTS Lab Engineer functions for timely installations and upgrades. Conduct thorough investigations of non-compliance issues, establishing effective corrective and preventive measures. Act as the primary point of contact for projects, ensuring seamless execution from initiation to completion. Maintain strong relationships with internal and external stakeholders to support quality and regulatory compliance. Lead team efforts in regulatory inspections and corporate audits, demonstrating ownership and expertise. Qualifications Bachelor’s Degree in Science or IT Discipline. Minimum of 5 years of experience in a pharmaceutical setting with IT or QC focus. Expertise in laboratory systems including LIMS, SAP, and Empower is advantageous. Strong attention to detail, with a proven track record of right-first-time outcomes. Excellent problem-solving skills and adaptability to new requirements. Demonstrated leadership in managing teams, setting annual goals, and improving team performance. Comprehensive understanding of GMP requirements and regulatory standards. Superior communication skills, both verbal and written, paired with strong interpersonal abilities. This role offers an exciting opportunity to lead groundbreaking digital transformation initiatives within our QA organisation. If you are a strategic thinker with a drive for excellence and innovation, apply now to join AbbVie's talented team! Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit here . US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more. #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 We are recruiting a Maintenance Supervisor to join our team in Cork . This position reports to the Operations Engineering Manager. This Maintenance Supervisor manages day-to-day Maintenance Department activities on site to ensure that all products are manufactured to GMP guidelines. The successful candidate will be responsible for driving a culture of continuous improvements and maintenance excellence through our MEP (Maintenance Excellence Programme). They will also ensure that the Equipment P.M & Calibration schedule, stores stocks and spare part list are maintained and up to date. Roles and Responsibilities Staff organization within the department including holiday cover and TMS review. Ensure that maintenance technicians are adequately trained, equipped, and motivated so that the maintenance program can be accomplished in a safe, timely, and cost-effective manner. Maintain training and safety awareness records and attendance records and ensure that all maintenance technicians are trained on the most updated version of the operating procedures. Responsible for all facility and live utility maintenance and upkeep. Preventative Maintenance / Calibration organization, control, and reporting. Work Request organization, control, and reporting. Assist in the preparation of departmental budgets. Establish and maintain computerized maintenance management system (CMMS) for tracking work orders, spare parts, time allocation and maintenance history of plant equipment. Maintain and is responsible for Calibration systems and compliance, including discrepancies, KPIs, SOPs related to calibrations. Department Audit Leader. Supervision and coordination of Reliability Engineering activities including Department Metric reporting to Management and external stakeholders, analysing data from QA relating to equipment malfunctions, with a view to improving equipment availability and reducing instances of downtime. Anticipate and solve problems in a timely manner and identify opportunities for improvement. Initiate and carry out projects that improve efficiency and/or reduce operating costs. Track, analyse and improve key maintenance parameters such as asset utilization, maintenance cost, PM compliance, schedule compliance, etc. Play an active role in Change Control committee for equipment changes. Conduct employee performance reviews based on job descriptions to determine competency, knowledge, and contribution of the maintenance technicians. Ensure statutory inspections relating to the maintenance department are always achieved. Directs, maintains, and enforces the safety program for the maintenance department; reviews safety records to uphold standards of maximum safety for all maintenance technicians. Qualifications Craft Qualification in electrical or mechanical trades. Minimum of 3 years experience in the pharmaceutical industry or similar environment. Computer literate - MS Word, Excel, Access, Outlook. Excellent communication and interpersonal skills. Strong problem-solving skills. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit this link . US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: this link . #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 We are looking for an experienced Project Engineer to join our engineering team in Carrigtwohill, Cork. This position reports to the Capital Project Manager. This is an 18-month Fixed Term Contract. This is a varied role, and you will be involved in everything from completing feasibility studies to leading commissioning and validation activities at a growing pharmaceutical manufacturing plant. Roles and Responsibilities Project management of the execution of capital engineering projects within the site, following the AbbVie Project Lifecycle approach. Support the Operations Engineering Team in controlling uptime of process equipment and optimizing efficiencies both in equipment and process performance. Improve the operations and reliability of equipment and processes by the successful identification and implementation of continuous improvement initiatives. Liaise with Internal/External Engineering Personnel and contract maintenance providers in maintaining, troubleshooting and installing/commissioning equipment. Leadership of equipment commissioning and validation activities as part of capital project execution. Work closely with cross-functional teams from other departments to deliver the site capital project portfolio. Prepare feasibility studies and budget management for all assigned capital projects. Support all major site initiatives and site core goals. Prepare Requests for Capital Expenditure (RCE) for site capital projects. Liaise with Global Engineering as required – eCOPs (engineering communities of practice), Engineering forums, etc. Responsible for all Engineering contractor management on-site, required to deliver capital projects i.e. ensure safety standards are met, and safe working practices adhered to at all times – RAMS, permit to work, training records, etc. Qualifications Essential Requirements Degree in a relevant Engineering subject area– Chemical/Process/Mechanical Engineering preferred. Strong previous pharmaceutical experience is essential (minimum 7-10 years). Knowledgeable/competent with executing change control. Knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry. Demonstrated relevant site experience of one or more of the below: Oral Solid Dose (OSD) equipment (tablet press, roller compaction, tablet coater, material handling – post hoists, blenders, milling – conical mills, etc). Cleanroom processing/utilities – HVAC, CIP systems, Purified water generation and distribution systems, Nitrogen, etc. Nice to have experience Experience of process engineering, with relevant experience of batch processing, automation, project management, commissioning and validation, equipment reliability and continuous improvement is desirable. Trackwise change control system experience. Electrical background – competency with electrical system design & installation (process equipment and site electrical infrastructure), familiar with ATEX regulations and requirements is beneficial. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit here . US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more. #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 We are currently seeking a dynamic and detail-oriented Supervisor for the QC Lab located on Manorhamilton Road, Sligo . This pivotal role is responsible for delivering an effective testing and analytical service to ensure that our plant's products consistently meet specified standards. As an important part of the quality control team, the Supervisor will take full accountability for compliance, documentation, equipment maintenance, and training within the QC Lab. This position is ideal for an individual who is passionate about quality assurance and possesses the skills needed to lead teams, optimize lab operations, and ensure that safety and quality standards are not only met but exceeded. Responsibilities Ensure Laboratory Documentation and Systems comply with Data Integrity policies. Understand and apply Regulations for Laboratory Data Integrity. Coach and guide analysts to optimize performance. Boost team efficiency and adhere to compliance timelines. Collaborate with the lab manager to enhance laboratory performance. Resolve analytical deviations promptly. Maintain 6S excellence and promote a quality culture. Ensure proper equipment use and maintenance. Support lab projects and develop procedures. Comply with EHS standards and Compendia testing requirements. Conduct document reviews and develop training materials. Oversee equipment calibration and team performance management. Qualifications Bachelor's degree in a relevant Science discipline. Minimum 4 years of analytical experience in the pharmaceutical industry. Expertise in HPLC, GC, LCMS, GCMS, and other analytical techniques. Strong regulatory knowledge and experience with analytical equipment. Preferred experience in product and method transfers. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit here . US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more. #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 We have an exciting new opportunity for an NPI Product Lead to join our Technical Operations team in Sligo. This position reports to the NPI Technical Manager. The successful candidate will provide technical support and day-to-day program management to all NPI across the site. Roles and Responsibilities Lead and support New Product Introduction activities for product, processes, and technologies from early-stage development through PPQ. Provide technical direction, oversight, and coordinate support for NPI activities within biological manufacturing area. Work closely with internal and external program management to ensure alignment on NPI schedules. Resource planning to ensure the required personnel are available to support manufacturing operations during NPI executions and ensure operations run safely and efficiently. Provide direct interface as a subject matter expert with QA department, HPRA, FDA and applicable health authority and internal audits. Drive innovation and continuous improvement. Provide leadership and mentoring for operations personnel during NPI activities. Collaborate closely with external partners to ensure engagement, alignment, and open communication during NPI activities. Collaborate with external and internal partners to influence the design and implementation of robust process control strategies and process risk assessments. Generation of product transfer documentation to attest the completion of product transfer deliverables in advance of the applicable product transfer stage gate review. Ensure ongoing compliance with cGMP and EH&S practices. Participate in NPI project gate reviews. Interface with internal auditors and outside regulatory agencies/auditors as the subject matter expert for new products and technology transfers. Provide technical input, review/approval for documentation associated with NPI activities. Qualifications Bachelor’s degree in engineering, science or closely related subject area. 5+ years experience in Pharmaceutical or Bio Industries with a minimum of 2 years experience in a similar role. Strong technical and operational knowledge of unit operation within an aseptic fill finish facility. Career history marked by a consistent series of technical contributions and accomplishments. Recognition given to significant contribution to product or process development or improvement through creative application of technical effort. Excellent critical thinking skills and the ability to influence cross-functional teams are essential. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit this link . US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: this link . #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 The Category Manager leads implementation of category procurement strategy, developed in partnership with Category Directors and VP-level business stakeholders. This role oversees the execution of the end-to-end procurement process, managing a team of Specialists to ensure excellence in all activities and compliance to policy. The Category Manager is responsible for developing team capabilities and assisting leadership in identifying workforce planning needs. Partner with Director/VP-level business or functional stakeholders to develop category-specific procurement strategies and contribute to the development of a comprehensive annual strategic plan for the relevant category, incorporating category strategies that align with overall business goals. Relay insights and market intelligence from team analysis to Directors and Associate Directors to inform strategic decision-making, staying abreast of industry trends, emerging technologies, and market dynamics. Manage strategic value drivers with key category suppliers to secure collaborative partnerships that challenge the status quo to achieve cost savings, optimize processes, and enhance overall procurement value. Manage and monitor supplier performance on sustainability and environmental, social, and governance (ESG) measures, working alongside suppliers to enhance sustainable and responsible sourcing practices. Enable Supplier Relationship Management (SRM) strategies, driving innovation with key category suppliers and collaborating to enact creative and cutting-edge solutions to deliver on long-term business needs. Implement mitigation strategies to proactively manage procurement risk across the relevant category, overseeing process and policy compliance. Ensure effective project management from initiation to completion, managing and driving cross-functional teams to deliver strategic category-related projects. Implement opportunities for process optimization and efficiency gains, leveraging data analytics to develop long-term continuous improvement programs that achieve strategic objectives. Assist with the end-to-end procurement process from sourcing strategy to contract negotiation and execution, enabling negotiations with category suppliers and facilitating decisions by conducting required analysis and preparation. Manage a team, monitoring and reporting progress toward performance targets. Identify capability gaps and assist in developing focused action plans to address workforce requirements and team needs. Qualifications Bachelor’s degree in Business Administration, Supply Chain Management or related field. Master’s degree is preferred. Minimum of 7 years of experience in procurement, supply chain, or related business or operations function. Previous experience managing teams in a procurement function and leading supplier relationships. Strong proficiency in Microsoft Office suite (Power Platform). Knowledge of the pharmaceutical industry is preferred. Specific and tactical expertise in category management, including market analysis, cost and financial assessment, ensuring strategic and informed procurement decisions. Ability to assist in negotiation and bidding, adept in implementing complex projects with a focus on effective change management. Strong capacity and experience building and managing collaborative supplier relationships, aligning procurement activities with business needs. Innovative problem-solving skills combined with a solution-oriented mindset, enabling creative approaches and influential communication at all organizational levels. High cross-functional collaboration abilities and teamwork skills, effectively navigating and coordinating diverse team dynamics. Strong interpersonal skills and emotional intelligence, facilitating empathetic interactions, effective communication, and robust relationship-building across a matrixed organization. Impactful executive functioning abilities and autonomous work ethic, maintaining efficient performance in challenging situations and building consensus in decision-making. Key Stakeholders Site or function leaders, finance staff and external suppliers. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit this link . US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more. #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 We are currently hiring a QC Metrology & Informatics Chemist to join our team in Clonshaugh in Dublin for a Fixed Term Contract of 12 months. The QC metrology & Informatics chemist is responsible for assisting in the management and qualification of laboratory instrumentation and computer systems through the relevant quality systems to the effective/final state ready for use. This person oversees and serves as a super user/resource for Abbvie QC for the ALEXIS LIMS, Empower, VelQuest Smartlab software and any other laboratory software systems. The QC metrology & Informatics support chemist performs GMP data review of laboratory projects associated with equipment calibration and preventative maintenance records. This person is expected to adhere to all cGMP compliance and regulatory mandates and quality requirements, and comply with all SOPs and Abbvie policies and procedures in the performance of job duties. This position reports to the QC Supervisor. Build and maintain specifications in the ALEXIS LIMS system. Build and maintain sessions in VelQuest Smartlab. Administration of laboratory software systems. Maintain data integrity and ensure compliance with FDA, GLP, QSR and cGMP regulations, as well as with company SOPs and specifications. Draft, review, and approve validation and qualification documentation for analytical software. Draft, review, and approve SOPs, forms, and associated documentation with analytical equipment. Management of laboratory instruments and standards through Labware LIMS. Perform routine review of documentation generated by the QC laboratory, such as auditing laboratory data and supporting documentation (instrumental printouts, COAs, chemist notebooks, cumulative stability tables, protocols, reports, laboratory investigations, analytical test methods etc.) generated to support equipment qualification and calibration for accuracy, completeness, and compliance to requirements. Initiate and facilitate Change Management Requests. Author documents that ensure cGMP compliance, such as analytical test methods, analytical test method development reports, method validation protocols and reports, method verifications protocols and reports, and instrumentation qualification documentation (URS/IQ/OQ/PQ). Seek process innovation and continuous process improvement in laboratory area. Complete and conform to all training requirements for job role, including company-required and job-specific training. Qualifications Bachelor’s Degree or above in Chemistry or related Science 3-5 years relevant Quality Control experience or equivalent combination of education and experience Experience in pharmaceutical manufacturing facility. Demonstrate knowledge of cGMP requirements and practices including extensive knowledge of the USP and FDA Guidance Documents relating to the pharmaceutical Quality Control Laboratory. Demonstrate competency in review of data generated by QC laboratory as attention to detail is a requirement of the position. Demonstrate strong organizational skills and the ability to communicate across multiple departments. Demonstrate strong analytical laboratory skills and laboratory troubleshooting abilities. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit this link . US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: this link . #J-18808-Ljbffr
