Principal Engineer, Digital Regulatory Assurance (Life Sciences)

Company Description 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 Principal Digital Regulatory Assurance is responsible for ensuring that AbbVie's IT operations and software lifecycle processes fully comply with regulatory requirements and corporate standards.

This role provides leadership in defining, implementing, and optimizing quality systems through digital enablement and AI-driven solutions, and involves direct collaboration with cross-functional teams, Business stakeholders, and the Business Technology Services (BTS) Quality organization. This techno-functional expert transforms traditional quality assurance by implementing automation frameworks and DevOps best practices that enhance efficiency, reduce cycle times, and ensure regulatory compliance while optimizing CI/CD pipelines  The Principal Digital Regulatory Assurance will provide oversight of quality activities, especially across Technology Lifecycle process monitoring and incident management, drive improvement initiatives, troubleshoot IT quality issues, and support all phases of the IT solution lifecycle.

The incumbent acts as the primary point of contact between business units and quality teams, ensuring mutual understanding of needs and maintaining effective service agreements.  Key Responsibilities:  Develop, implement, and champion solution/change strategies that align with organizational objectives and evolving regulatory requirements, leveraging AI-powered solutions and automation to enhance compliance monitoring and operational efficiency.  Leverage extensive DevOps process and toolchain expertise to standardize, streamline, and simplify DevOps practices by integrating and optimizing tools across CI/CD pipelines, automated testing, deployment, and monitoring capabilities.  Lead continuous improvement and digital enablement initiatives, focusing on modernizing quality assurance frameworks and driving adoption of advanced automation, validation pipelines, and intelligent process monitoring.  Drive automation of Software Lifecycle (SLC) processes by developing and deploying automated validation tools, intelligent documentation generation, and workflow solutions to reduce manual effort and cycle times.  Manage technology lifecycle process monitoring, establish automated dashboards and alerts for system performance, and implement targeted improvements to ensure optimal compliance and efficiency.  Serve as the primary point of contact for incident management related to quality events and deviations, coordinate investigations, root cause analysis, and ensure effective corrective actions.  Monitor and update SLC procedures in response to changes in regulatory standards and industry best practices.  Represent SQA on strategic forums, steering committees, and regulatory engagements; communicate quality outcomes, audit results, and improvements to partners and stakeholders.  Support and manage regulatory audits and inspections, oversee CAPA investigations and remediation activities, ensuring timely implementation and closure.  Provide expert mentorship on DevOps best practices, automation, computerized system quality, policy interpretation, and new quality technologies.  Lead training initiatives for internal