GxP Integration Engineer for Quality Systems

ABBVIE; North Chicago (IL); On-site; USD 79,000 - 141,000; Full time

Job summary

AbbVie is seeking a Software Engineer to independently design and optimize system integrations for Quality and GxP-regulated software environments. You will deliver compliant, reliable data flows across Quality, Laboratory, Validation, and Manufacturing IT platforms, driving continuous improvement and technical leadership.

Responsibilities include leading integration design for LIMS, QMS, and document management, collaborating with Quality, IT, validation, and vendors, and ensuring adherence to

Qualifications

• 5+ years IT or software engineering experience, with GxP/Quality system integration and validated computer systems.
• Experience with REST/SOAP APIs, ETL tools, middleware, ESB in regulated contexts.
• SDLC and software validation knowledge for regulated environments (21 CFR Part 11, GAMP 5).
• Strong documentation and cross-functional leadership skills.

Responsibilities

• Lead design and implementation of integration solutions for Quality systems (LIMS, QMS, document management) enabling data interoperability.
• Collaborate with Quality, IT, Validation and vendors to define requirements and architecture that meet compliance needs.
• Optimize and maintain interfaces and APIs for secure, validated data exchanges with ERP, MES, cloud and on‑prem databases.
• Drive software delivery activities including requirements, development, testing, qualification, and deployment under regulated frameworks.
• Create and maintain technical documentation, integration specs, workflow diagrams, and validation protocols.

Education

Bachelor’s Degree with 5 years’ experience

Master’s Degree with 4 years’ experience

Tools

REST/SOAP APIs

ETL tools

Middleware/ESB

Cloud (AWS/Azure)

Data security in regulated environments

Job description

AbbVie is seeking a Software Engineer to independently design and optimize system integrations for Quality and GxP-regulated software environments. You will deliver compliant, reliable data flows across Quality, Laboratory, Validation, and Manufacturing IT platforms, driving continuous improvement and technical leadership.

Responsibilities include leading integration design for LIMS, QMS, and document management, collaborating with Quality, IT, validation, and vendors, and ensuring adherence to