Principal Engineer, Quality Assurance, Dev-Ops

Job Description The Principal Quality Engineer – DevOps is responsible for ensuring that AbbVie's IT operations and software lifecycle processes fully comply with regulatory requirements and corporate standards. The 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 Quality Engineer – DevOps 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 teams and business stakeholders on IT Quality standards, SLC procedures, and new tools/technologies. Oversee documentation and evidence management to maintain compliance and facilitate investigations and audit readiness. Assist Center of Excellence (CoE) leadership with SLC communications, newsletters, and internal coordination efforts. Escalate and resolve significant quality exceptions, risks, and issues with minimal supervision. Engage in infrastructure change management and risk review activities, submit timely risk assessments to maintain compliance and business continuity. Develop, monitor, and interpret SQA metrics and trends using automated analytics, identifying quality gaps and preparing actionable dashboards and reports for senior leadership. Qualifications Required: Bachelor’s degree plus 7 years of experience, master’s degree plus 6 years of experience, PhD plus 2 years of experience. Proven expertise in DevOps toolchains (e.g., Jira, Confluence, qTest, Jenkins, GitLab, AWS, Azure DevOps), automation pipelines, and CI/CD. Experience managing SQA practices, validation strategy, risk and incident management/mitigation. Experience supporting regulatory audits and compliance (FDA or similar agencies). Strong skills in analytics, project management, process improvement, and cross‑functional collaboration. Ability to coach teams in policy, SLC execution, and regulatory requirements. Knowledge of Computer Software Assurance (CSA), digital transformation in quality, and contemporary validation practices. Professional certifications (e.g., ASQ CQA, PMP, Six Sigma) preferred. Preferred: Supervisory experience. Professional certifications (e.g., ASQ CQA, PMP, Six Sigma). Proven expertise in life‑sciences industry DevOps toolchains and automation. Compensation and Benefits Competitive base pay range based on job grade, location, and experience. Actual compensation will depend on geographic location and may be modified in the future. Comprehensive benefits package including paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) for eligible employees. Eligibility to participate in long‑term incentive programs. Equal Opportunity Statement 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 Allergan