Abbott Laboratories

Abbott Laboratories seeks a Senior Solution Architect to design and govern scalable, secure solutions supporting diagnostics, devices, and pharma platforms. You will define target architectures, lead end-to-end solution designs, and ensure interoperability, data integrity, and regulatory compliance across global systems. Partnering with R&D, product, and IT teams, you'll translate business and clinical needs into technical roadmaps, guide implementation teams, and drive architecture standards that enable innovation, reliability, and performance for life-changing healthcare technologies in a highly collaborative, inclusive environment. Responsibilities Design and document scalable, secure enterprise solutions for diagnostics, devices, and pharma platforms. Define target architectures and roadmaps aligned with business and regulatory requirements. Lead end-to-end solution design across applications, data, and integration layers. Ensure interoperability, data integrity, and compliance with healthcare and Gx P standards. Collaborate with R&D, product, and IT teams to translate requirements into architectures. Provide technical leadership and guidance to engineering and implementation teams. Establish and enforce architecture principles, patterns, and best practices. Evaluate and select technologies, platforms, and integration approaches. Support solution reviews, risk assessments, and remediation plans. Contribute to continuous improvement of architecture standards and governance. Required Skills Enterprise solution architecture Cloud platforms (AWS/Azure/GCP) Microservices and API design Data integration and interoperability (HL7/FHIR) Security and compliance (HIPAA, Gx P) Biotech/pharma domain knowledge Systems design and documentation Stakeholder management Architectural governance and best practices Dev Ops and CI/CD

Abbott Laboratories seeks an IT BRM to align technology solutions with our biotechnology and pharmaceutical business goals. In this role, you will act as a strategic partner to business leaders, translating needs into IT roadmaps that support diagnostics, medical devices, and pharma operations. You will manage demand, shape portfolios, and guide projects from idea to value realization, ensuring compliance in a regulated environment. Collaborating across global teams, you'll drive innovation, data-driven decisions, and continuous improvement, while contributing to Abbott's mission of improving health and quality of life worldwide. Responsibilities Serve as primary liaison between IT and business units within biotech and pharmaceutical operations Define and prioritize IT demand aligned with business strategy and regulatory requirements Develop and maintain IT roadmaps supporting diagnostics, devices, and pharma portfolios Lead requirements gathering, solution evaluation, and business case development Coordinate cross-functional teams to deliver projects on time, within scope, and budget Monitor solution performance and drive continuous improvement and value realization Support governance, risk, and compliance activities for regulated IT systems Communicate status, risks, and issues to senior stakeholders and propose mitigation plans Required Skills IT business relationship management Biotech and pharmaceutical domain knowledge IT portfolio and demand management Requirements gathering and analysis Project and program management Regulated environment and Gx P compliance Data and analytics solutions Stakeholder management and communication Vendor and solution evaluation IT governance and risk management

Abbott Laboratories seeks a Cybersecurity Manager to lead security strategy and operations across its biotechnology and pharmaceutical ecosystem. In this role, you will design and implement security controls to protect sensitive data, manufacturing systems, and cloud platforms supporting life changing healthcare products. You will manage threat monitoring, incident response, and vulnerability management while ensuring compliance with NIST, ISO 27001, and healthcare regulations. Collaborating with IT, R&D, and business teams, you will embed security by design, guide a high performing security team, and help advance Abbott's mission of improving global health. Responsibilities Develop and execute cybersecurity strategy aligned to Abbott's biotech and pharmaceutical operations. Lead security operations, including monitoring, threat detection, and incident response. Implement and manage security controls, tools, and policies across on prem and cloud environments. Oversee vulnerability management, risk assessments, and remediation plans. Ensure compliance with healthcare and pharma regulations (e.g., FDA, HIPAA) and security frameworks (NIST, ISO 27001). Partner with IT, R&D, manufacturing, and business leaders to embed security in products and processes. Manage third party and supply chain security risks. Lead and mentor cybersecurity analysts and engineers. Develop and deliver security training and awareness programs. Report on security posture, risks, and incidents to senior leadership. Required Skills Cybersecurity strategy and governance Security operations and SIEM tools Incident detection and response Vulnerability management Network and endpoint security Cloud security (AWS/Azure/GCP) Identity and access management (IAM) Regulatory and compliance (FDA, HIPAA, NIST, ISO 27001) Risk assessment and management Security architecture and design

Abbott Laboratories seeks an IT Director, Data & AI Architecture to shape enterprise data and AI strategy for its biotechnology and pharmaceutical portfolio. This role leads design of secure, scalable cloud and data platforms, enabling advanced analytics and AI/ML for global healthcare products and operations. You will define reference architectures, data governance, and integration patterns, partnering closely with R&D, diagnostics, and business leaders. The director mentors technical teams, evaluates emerging technologies, and drives innovation that improves patient outcomes and operational excellence in a collaborative, mission-driven environment. Responsibilities Lead enterprise Data & AI architecture strategy supporting Abbott's biotechnology and pharmaceutical solutions Design scalable cloud, data, and analytics platforms enabling advanced insights and AI/ML capabilities Establish data governance, security, and compliance standards across global systems Partner with R&D, IT, and business stakeholders to align data architecture with product and clinical goals Evaluate and select technologies, tools, and platforms for data integration, storage, and AI workloads Guide solution architects and engineers, setting reference architectures and technical roadmaps Ensure reliability, performance, and interoperability of data ecosystems across regions Drive innovation in data engineering, MLOps, and real-time analytics to improve patient and business outcomes Required Skills Enterprise data architecture Cloud platforms (AWS/Azure/GCP) Data warehousing and lakehouse design ETL/ELT and data integration AI/ML platforms and MLOps Data governance and security API and microservices architecture SQL and distributed data technologies Regulated environment (Gx P, HIPAA) knowledge Leadership and stakeholder management

Abbott Laboratories is seeking an Application Architect to design secure, scalable solutions that power innovative healthcare products. In this role, you'll define end-to-end application architectures, lead cloud-native and integration designs, and ensure systems meet performance, security, and regulatory requirements. You'll collaborate with cross-functional teams, guide development standards and best practices, and provide technical leadership while contributing to Abbott's mission of improving global health through advanced technologies. Responsibilities Design and document end-to-end application architectures for healthcare solutions Lead cloud-native and integration solution designs across platforms and services Ensure applications comply with security, privacy, and regulatory requirements Collaborate with cross-functional teams to translate business needs into technical designs Define and enforce development standards, patterns, and best practices Guide performance, scalability, and reliability improvements for critical systems Provide technical leadership and mentorship to development teams Evaluate and recommend technologies, tools, and platforms to support product roadmaps Required Skills Application architecture design Cloud platforms (AWS/Azure/GCP) Microservices and APIs Enterprise integration patterns Database design (SQL/No SQL) Security and compliance (HIPAA/FDA/21 CFR Part 11) Dev Ops and CI/CD pipelines Containerization (Docker/Kubernetes) Solution documentation and modeling (UML/Archimate) Performance and scalability optimization

Abbott Laboratories seeks a Senior IT Manager, Global Data and Analytics to lead enterprise data strategy across its biotechnology and pharmaceutical businesses. In this role, you will own the vision, roadmap, and execution of global data platforms, overseeing data engineering, BI, and analytics teams that power critical scientific, commercial, and operational decisions. Partnering with leaders across R&D, diagnostics, and commercial functions, you will translate complex business needs into scalable, secure, and compliant data solutions. You will champion data governance, quality, and advanced analytics adoption, ensuring alignment with regulatory standards while fostering an inclusive, growth-oriented, and innovative culture. Responsibilities Lead global data and analytics strategy to support Abbott's biotechnology and pharmaceutical operations Oversee design, delivery, and governance of enterprise data platforms and analytics solutions Partner with business and scientific leaders to translate needs into scalable data products and dashboards Manage data engineering, BI, and analytics teams; mentor and develop technical talent Establish data quality, security, and compliance standards across regions Drive adoption of advanced analytics, including AI/ML, to improve decision-making and patient outcomes Collaborate with IT, R&D, and commercial teams on cross-functional initiatives Manage vendor relationships, budgets, and project portfolios Ensure solutions comply with healthcare, privacy, and regulatory requirements (e.g., HIPAA, Gx P) Continuously improve processes, tools, and architectures to enhance performance and reliability Required Skills Data warehousing and data lake architecture (e.g., Snowflake, Redshift, Big Query, Azure Synapse) SQL and relational database design Cloud platforms (AWS, Azure, or GCP) for data and analytics workloads ETL/ELT and data integration tools (e.g., Informatica, Talend, dbt) Business intelligence and visualization tools (e.g., Power BI, Tableau, Qlik) Data governance, data quality, and master data management Advanced analytics and machine learning concepts and tooling (e.g., Python, R, Spark) Information security, privacy, and regulatory compliance in healthcare/life sciences IT project and portfolio management, including Agile practices People leadership, stakeholder management, and cross-functional collaboration

Abbott Laboratories is seeking an IT Senior Manager to lead strategic technology initiatives supporting our global healthcare business. In this role, you will oversee IT teams delivering secure, reliable infrastructure and applications in a highly regulated environment. You will partner with business leaders to define roadmaps, drive complex projects from concept to deployment, and ensure compliance with security and regulatory standards. You will champion innovation, standardization, and continuous improvement while fostering an inclusive, growth-oriented culture. Responsibilities Lead IT strategy and roadmap to support Abbott's global healthcare operations. Manage and mentor IT teams delivering infrastructure, applications, and services. Oversee end-to-end delivery of IT projects, ensuring scope, budget, and timelines are met. Ensure compliance with security, privacy, and regulatory requirements (e.g., FDA, Gx P). Partner with business leaders to translate needs into scalable technology solutions. Drive continuous improvement, standardization, and automation across IT services. Manage vendor relationships and technology contracts to optimize value and performance. Monitor KPIs, service levels, and risks, implementing corrective actions as needed. Champion inclusive, collaborative culture and support talent development within IT. Required Skills IT strategy and roadmapping Enterprise infrastructure and/or applications management Project and program management Regulatory and compliance (e.g., FDA, Gx P, SOX) Information security and risk management Vendor and contract management IT service management (ITIL) Cloud platforms (e.g., AWS, Azure) Budgeting and financial management for ITStakeholder communication and leadership

Abbott Laboratories seeks an IT Quality & Regulatory Assurance Manager to lead IT compliance across biotechnology and pharmaceutical operations. In this role, you will own IT quality frameworks, ensuring GxP, FDA, 21 CFR Part 11, and ISO compliance for critical systems. You will drive computer system validation, change control, and risk management, and lead audit readiness for internal and external inspections. Partnering closely with global IT, QA, and business teams, you will embed quality by design, implement continuous improvement, and provide training in a collaborative, mission-driven environment that supports career growth and work-life balance. Responsibilities Lead IT quality and regulatory assurance activities for Gx P-relevant systems and processes. Develop, implement, and maintain IT quality management procedures and documentation. Ensure compliance with FDA, 21 CFR Part 11, Gx P, ISO and other applicable regulations and standards. Oversee computer system validation, change control, and risk management for IT solutions. Plan and support internal and external audits and inspections, driving remediation and CAPAs. Partner with IT, QA, and business stakeholders to embed quality by design into projects. Monitor, analyze, and report on IT quality metrics and continuous improvement initiatives. Provide training and guidance on IT quality and regulatory requirements to teams. Review and approve IT deliverables, including requirements, testing, and validation packages. Collaborate globally to harmonize IT quality practices and support corporate initiatives. Required Skills IT quality management Gx P compliance21 CFR Part 11 Computer system validation (CSV) Change control and configuration management Risk management in regulated environments Audit planning and execution CAPA management ISO 9001/13485 standards Regulated documentation and SOPs Quality metrics and reporting Project management Stakeholder management Training on compliance and quality processes Medical device/pharma regulatory knowledge

Abbott Laboratories is seeking a Staff Equipment and Automation Engineer to lead design, implementation, and optimization of automated production systems for diagnostics and medical products. In this role, you will own full lifecycle equipment projects-from requirements and concept development through installation, validation, and continuous improvement-ensuring reliability, compliance, and throughput in a regulated (FDA/ISO) environment. You will collaborate with manufacturing, quality, and R&D to introduce new technologies, drive root cause analysis, reduce downtime, and standardize best practices across sites while mentoring junior engineers. Responsibilities Lead design, commissioning, and optimization of automated manufacturing and test equipment Plan and execute equipment validation (IQ/OQ/PQ) and documentation in compliance with FDA/ISO and c GMPDrive continuous improvement to increase throughput, OEE, and equipment reliability Implement automation solutions including PLCs, robotics, vision systems, and data acquisition Lead root cause investigations and corrective actions for equipment and process issues Collaborate with Manufacturing, Quality, and R&D on new product introductions and tech transfers Manage capital equipment projects including scope, schedule, budget, and vendor coordination Develop and maintain technical documentation, SOPs, and maintenance standards Ensure equipment safety, regulatory compliance, and audit readiness Mentor junior engineers and technicians, sharing best practices and technical expertise Required Skills Equipment validation (IQ/OQ/PQ) Automation system design (PLC/SCADA/HMI)c GMP and FDA/ISO regulatory compliance Process optimization and OEE improvement Root cause analysis and corrective actions Project management for capital equipment Technical documentation and protocols Data acquisition and manufacturing analytics Robot/automated material handling systems Cross-functional collaboration with QA/RA/Operations

Abbott Laboratories seeks a Manufacturing Automation Engineer II to design, implement, and optimize automated systems for biotech and pharmaceutical manufacturing. In this role, you will develop and program PLCs and HMIs, integrate robotics and control systems, and support validation activities to meet GMP and FDA requirements. You will troubleshoot automation issues, analyze production data, and drive process improvements to enhance quality, throughput, and reliability. Collaborating with cross-functional teams, you'll support global health-impacting products while growing in a diverse, learning-focused, and mission-driven environment. Responsibilities Design, program, and maintain PLC, HMI, and control systems for biotech manufacturing lines Integrate robotics and automation equipment to improve safety, throughput, and consistency Support validation activities (IQ/OQ/PQ) and ensure GMP/FDA compliance for automated systems Troubleshoot automation issues and implement sustainable corrective and preventive actions Analyze production and equipment data to drive process optimization and reliability improvements Collaborate with engineering, quality, and operations to define and execute automation projects Develop and maintain technical documentation, SOPs, and change control records Support commissioning, qualification, and startup of new or upgraded automated equipment Provide training and technical support to operations and maintenance teams on automation systems Contribute to continuous improvement, standardization, and digitalization initiatives across the plant Required Skills PLC programming SCADA/HMI development Industrial robotics integration Control system design Validation and IQ/OQ/PQGMP/FDA compliance Data acquisition and analysis Process automation troubleshooting Industrial networking (Ether Net/IP, Profibus) Technical documentation

Abbott Laboratories is seeking a Senior Automation Engineer to drive advanced automation solutions for our Biotechnology & Pharmaceuticals R&D teams. In this role, you will design, implement, and optimize automated laboratory and pilot-scale systems, integrating robotics, instruments, and data platforms to accelerate experimentation and development. You will lead full lifecycle automation projects, ensure GMP/GxP and data integrity compliance, and troubleshoot complex controls issues. Working in an inclusive, mission-driven culture, you will collaborate across functions, mentor junior engineers, and help shape innovative, global health technologies while benefiting from strong career growth and competitive rewards. Responsibilities Design, implement, and optimize automation solutions for R&D laboratories and pilot processes. Integrate robotics, instruments, and data systems to streamline biotech experimentation and analysis. Lead automation projects from requirements through deployment, validation, and documentation. Ensure compliance with GMP/Gx P, data integrity, and cybersecurity standards for automated systems. Troubleshoot and resolve complex automation, controls, and data integration issues. Collaborate with scientists, engineers, and IT to translate R&D needs into robust automated workflows. Develop and maintain PLC, SCADA, and scripting code for lab and pilot-scale equipment. Author and execute validation protocols (IQ/OQ/PQ) and change controls for automated systems. Mentor junior engineers and share best practices in automation and system design. Continuously assess emerging technologies to improve R&D productivity and reliability. Required Skills Automation engineering Robotics integration Bioprocess automation PLC programming SCADA systems Python or similar scripting Data acquisition systems Validation and IQ/OQ/PQGMP/Gx P compliance Risk and root-cause analysis

Abbott Laboratories seeks an Automation Engineer to design, implement, and optimize automated systems supporting biotech and pharmaceutical manufacturing. In this role, you will develop and maintain PLC, SCADA, and HMI solutions for production and diagnostic equipment, ensuring high reliability, data integrity, and compliance with GMP and FDA regulations. You will troubleshoot system issues, lead equipment integration and validation, and collaborate with cross-functional teams to drive process improvements. Abbott offers a mission-driven, inclusive culture with strong career development, global opportunities, and competitive benefits in a values-driven environment. Responsibilities Design, program, and maintain automation systems (PLCs, SCADA, HMIs) for production and diagnostic equipment. Ensure systems comply with GMP, FDA, and 21 CFR Part 11 requirements, including documentation and validation. Troubleshoot and resolve automation, controls, and integration issues to minimize downtime. Collaborate with cross-functional teams on new equipment commissioning and process improvements. Develop and maintain technical documentation, SOPs, and change controls for automated systems. Analyze system performance data to drive reliability, quality, and throughput improvements. Support audits, qualification, and validation activities for automated processes. Provide technical training and support to operations and maintenance teams. Required Skills PLC programming (e.g., Siemens, Rockwell) SCADA and HMI development Industrial automation and control systems design GMP and FDA regulatory compliance21 CFR Part 11 and data integrity Automation system validation and qualification Industrial networking and communication protocols Process control and instrumentation Technical documentation and change control Troubleshooting of electromechanical systems

Abbott Laboratories seeks a Process Development & Automation Engineer II to design, optimize, and automate processes supporting biopharmaceutical and diagnostic production. In this role, you will develop and scale process automation solutions, integrate equipment and control systems, and ensure robustness, yield, and compliance in a regulated environment. You will collaborate closely with R&D, manufacturing, and quality teams, analyze process data to drive improvements, support tech transfer, and maintain GMP-aligned documentation. Abbott offers a mission-driven, inclusive culture, strong career development, and the opportunity to impact global health through innovative technologies. Responsibilities Design and optimize automated processes for biopharmaceutical production and lab workflows Develop, validate, and scale-up process automation solutions from concept to implementation Collaborate with R&D, manufacturing, and quality teams to improve yield, reliability, and compliance Create and maintain technical documentation, SOPs, and validation protocols for automated systems Analyze process data to identify improvements, troubleshoot issues, and implement corrective actions Ensure processes meet regulatory, safety, and GMP requirements Support technology transfers and integration of new equipment and control systems Provide technical training and support to operations and engineering teams Required Skills Process development in biotech/pharma Automation systems (PLC, SCADA, DCS) GMP/Gx P compliance Process validation and qualification Statistical data analysis (DOE, SPC) Process control and instrumentation Technical documentation and SOP writing Scale-up and tech transfer Root cause analysis and troubleshooting CAD or process modeling tools

Abbott Laboratories is seeking an Equipment and Automation Engineer II to support biotechnology and pharmaceutical manufacturing operations. In this role, you will design, implement, and optimize automated equipment and control systems to improve reliability, throughput, and product quality in a regulated GMP environment. You will lead equipment qualification, support validation, develop and maintain SOPs, and drive root cause investigations. Partnering with manufacturing, quality, and R&D, you will execute continuous improvement projects, ensure regulatory compliance, and contribute to safe, efficient, and innovative production systems. Responsibilities Design, implement, and support automated equipment and control systems for biotech/pharma manufacturing. Lead and execute equipment qualification and support validation activities (IQ/OQ/PQ). Ensure equipment and automation systems comply with c GMP, FDA, and internal quality standards. Troubleshoot equipment and automation issues and drive root cause analysis and corrective actions. Develop and maintain technical documentation, including URS, SOPs, and validation protocols. Collaborate with manufacturing, quality, and R&D on process improvements and technology transfers. Identify and implement continuous improvement projects to enhance reliability, safety, and throughput. Support change control, risk assessments, and CAPA related to equipment and automation. Monitor equipment performance using data analysis and implement optimization strategies. Provide technical training and guidance to operations and maintenance teams. Required Skills Equipment validation (IQ/OQ/PQ) Automation/controls engineering (PLC, SCADA, HMI)c GMP and FDA/ISO regulatory compliance Process development and optimization Technical troubleshooting and root cause analysis Change control and CAPA systems Data analysis and reporting Technical documentation (URS, SOPs, protocols) Cross-functional project coordination Risk assessment (FMEA or similar)

Abbott Laboratories is seeking an IT Supplier Manager for Infrastructure & Strategic Services to oversee key technology vendors supporting global healthcare operations. In this role, you will manage end-to-end supplier relationships, negotiate contracts and SLAs, monitor performance, and drive cost optimization for infrastructure, cloud, and strategic IT services. You will partner with IT, procurement, security, and business leaders to align supplier capabilities with Abbott's mission-driven, innovative culture, ensuring compliance, risk management, and continuous improvement while supporting global scalability and reliability of critical IT services. Responsibilities Manage end-to-end relationships with IT infrastructure and strategic service suppliers Negotiate contracts, pricing, and SLAs to optimize value and performance Monitor supplier performance and drive continuous improvement initiatives Collaborate with IT, procurement, security, and business stakeholders on sourcing strategy Ensure compliance with corporate policies, regulatory requirements, and security standards Identify and mitigate supplier and third-party risk across critical IT services Support budgeting, forecasting, and cost optimization for IT supplier spend Lead periodic business reviews and governance forums with key vendors Support global scalability and reliability of infrastructure and cloud services Report supplier performance metrics and recommendations to IT leadership Required Skills IT vendor management Contract negotiation Service Level Agreement (SLA) management IT infrastructure and cloud services knowledge Third-party risk management IT procurement and sourcing Financial and cost analysis Stakeholder management and communication Governance and performance reporting Regulatory and compliance understanding (e.g., healthcare, data security)

Abbott Laboratories seeks an Automation Engineer I to support R&D teams developing innovative healthcare technologies. In this role, you will assist in designing, configuring, and testing laboratory automation systems, including instruments, robotics, and workflows. You will help execute experiments, collect and analyze data, and troubleshoot hardware and software issues. Working in a collaborative, mission-driven environment, you'll document work per quality standards and contribute to continuous improvement while growing skills through mentorship and learning opportunities. Responsibilities Support design, configuration, and testing of R&D automation systems and lab instruments. Develop, execute, and document test protocols, experiments, and validation activities. Troubleshoot automation hardware/software issues and implement corrective actions. Collaborate with scientists and engineers to translate experimental needs into automated workflows. Maintain accurate technical documentation, SOPs, and change records in compliance with quality standards. Analyze experimental and system performance data to optimize reliability and throughput. Assist in integration of new instruments, robotics, and software into existing platforms. Ensure adherence to safety, regulatory, and quality requirements (GMP/GLP, FDA, ISO). Required Skills Automation system design and configuration Laboratory instrumentation and robotics PLC or control system programming Scripting (e.g., Python, VBA) for workflow automation Test method development and execution Data analysis and reporting GMP/GLP and FDA/ISO quality compliance Technical documentation and SOP writing Troubleshooting of electro-mechanical systems Collaboration in cross-functional R&D teams

Abbott Laboratories is seeking a Global Supply Chain Solution Architect for Planning & Logistics to design and optimize end-to-end planning, distribution, and logistics capabilities across our worldwide network. In this role, you will define target processes, architect technology solutions (e.g., ERP, APS, and planning tools), and lead global deployments that enhance service, cost, and inventory performance. Partner with regional teams, IT, and business leaders to translate requirements into scalable solutions. Support continuous improvement, data-driven decision making, and standardization aligned with Abbott's mission-driven, inclusive culture. Responsibilities Design and optimize global supply chain planning and logistics processes and solutions Lead architecture and deployment of ERP and advanced planning systems across regions Translate business requirements into scalable technical and process designs Collaborate with IT, regional supply chain, and business leaders to align solutions with strategy Develop and monitor key supply chain performance metrics and analytics Drive standardization and continuous improvement initiatives across global operations Ensure solution compliance with regulatory, quality, and security standards in healthcare Support change management, training, and adoption for new tools and processes Required Skills Global supply chain design Demand and supply planning Logistics network optimization Advanced planning systems (SAP APO/IBP or similar) ERP integration Data analytics and KPIs Process improvement/Lean Six Sigma Stakeholder management Project management Change management

Job Description Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree. A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity Lead, manage, plan, and coordinate operational and administrative activities within the IT Quality and Regulatory Assurance area to achieve compliance with regulations and industry standards, while minimizing impact on Global IT Organizations. This role is not within the software testing organization. Accountable for global compliance to Abbott policies and procedures that have specific applicability in quality, including documentation and adherence to global regulations. What You'll Work On Software Life Cycle (SLC) Governance Serve as a subject matter expert for the Abbott Software Life Cycle process. Provide quality oversight and guidance throughout system planning, development, validation, implementation, maintenance, and retirement activities. Ensure compliance with applicable regulatory requirements and internal quality standards. Support development and delivery of SLC training and awareness initiatives. Promote a culture of quality, compliance, accountability, and continuous improvement Identify opportunities to improve compliance processes, quality system effectiveness, and operational efficiency. Quality Event Management / CAPA Quality event identification, assessment, investigation, documentation, and resolution for suspected policy, process, procedure, or system nonconformities. Ensure effective root cause analysis, corrective and preventive actions (CAPA), and verification of effectiveness. Quality System Documentation Development, review, approval, and maintenance of policies, processes, procedures, standards, and work instructions in alignment with Abbott Quality System requirements and regulatory expectations. Audit and Inspection Readiness Support internal audits, external audits, supplier audits, and regulatory inspections. Maintain inspection readiness through effective quality system monitoring, audit response management, and remediation activities. Quality Oversight and Business Partnership Provide independent quality oversight, direction, and consultation to project teams, system owners, and business stakeholders. Ensure business objectives, risk management considerations, and quality requirements are appropriately balanced and aligned. Risk Management and Compliance Decision Making Utilize risk-based approaches to assess compliance impacts and support informed business decisions. Escalate significant compliance risks and recommend appropriate mitigation strategies. Stakeholder, Relationship, and Escalation Management Build effective partnerships across Quality, Regulatory, IT, and Business functions. Manage complex stakeholder relationships and provide leadership through issue resolution and escalation processes. Influence decision-making at multiple organizational levels to achieve compliant business outcomes. Minimum Requirements & Qualifications: Minimum Qualifications: Bachelor's degree or equivalent experience 8+ years combined experience in software development, validation, and/or regulated quality systems (QMS/GxP/CAPA). 1-3 years' experience in a regulated software development / validation environment (QMS) 1-3 years' experience in GxP quality systems for IT, Pharma, or Device. Strong experience in leading software validation efforts, providing software quality assurance support, providing quality system support to IT systems. Knowledge of regulations and standards that affect the health care industry. Preferred Qualifications: Effective communication skills and collaboration skills. Knowledge of Software Lifecycle and software methodologies (SLC processes). Knowledge of AI types and AI validation methods. Knowledge of SaaS validation and compliance Supervisory Responsibilities Has direct/indirect reports. Responsibility for performance monitoring and resource allocation. May have responsibility for setting goals, performance assessments and developing growth plan for direct reports. Misc: This is an onsite role at Abbott location in IL This is not a remote role/opportunity. Apply Now Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at , on Facebook at , and on The base pay for this position is $99,300.00 - $198,700.00. In specific locations, the pay range may vary from the range posted.