Software Engineer

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 .

The Software Engineer will serve as a technical expert independently designing, implementing, and optimizing system integrations for Quality systems and GxP-regulated computer software delivery. This role focuses on enabling compliant, reliable, and scalable integration solutions across Quality, Laboratory, Validation, and Manufacturing IT platforms. The engineer ensures robust data flows, system interoperability, and adherence to software delivery and regulatory standards supporting quality initiatives. The role requires continuous improvement of integration methods, technical leadership in selecting emerging tools, and alignment with best practices in software validation for regulated environments. Responsibilities: • Lead the design and implementation of integration solutions for Quality systems, including LIMS, QMS, document management, and other computerized GxP systems, enabling seamless data interoperability. • Collaborate with cross-functional teams (Quality, IT, Validation, vendors) to define requirements, develop integration architectures, and ensure solutions meet business needs and compliance expectations. • Optimize and maintain interfaces/APIs for reliable, secure, and validated data exchanges between quality systems and enterprise platforms (ERP, MES, Cloud, on-premises databases). • Drive and contribute to computer software delivery projects, including requirements analysis, development, testing, qualification, and deployment activities within regulated frameworks (e.g., 21 CFR Part 11, GAMP 5). • Develop and manage technical documentation, integration specifications, workflow diagrams, and validation protocols supporting all integration and delivery work. • Serve as subject matter expert for system integration and quality computer system delivery best practices, sharing expertise, mentoring others, and providing technical guidance during audits or inspections. • Identify and implement process improvements, automation, and new technologies supporting integration reliability and compliance. • Facilitate vendor engagement for integration solutions, review contracts, gather cost estimates, and ensure partner compliance with AbbVie's Vendor Management policies. • Communicate project status, challenges, and risks to stakeholders, providing clear and actionable updates. • Ensure all integration and software delivery work is performed in alignment with AbbVie policies, GxP guidance, cybersecurity, and software development lifecycle (SDLC) standards.

Bachelor’s Degree with 5 years’ experience; Master’s Degree with 4 years’ experience At least 5 years' experience in IT or software engineering, with specific experience in GxP/Quality system integration and validated computer system implementation. Proficiency in integration technologies (e.g., REST/SOAP APIs, ETL tools, middleware, ESB) and experience with Quality systems common to the pharmaceutical industry. Demonstrated expertise in software validation, GAMP 5, 21 CFR Part 11, risk-based validation, and SDLC for regulated environments. Excellent communication, organizational, and cross-functional leadership skills. Experience engaging with affiliates, vendors, and project stakeholders to gather requirements, provide estimates, and ensure successful project delivery. Ability to manage multiple priorities, adapt to evolving project goals, and