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Software Engineer, Data Engineering, Systems Engineer

Job in North Chicago, Lake County, Illinois, 60086, USA
Listing for: BioSpace
Full Time position
Listed on 2026-08-28
Job specializations:
  • IT/Tech
    Data Engineering, Systems Engineer
Salary/Wage Range or Industry Benchmark: 110000 - 170000 USD Yearly USD 110000.00 170000.00 YEAR
Job Description & How to Apply Below

Company Description

Abb Vie’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 Abb Vie, please visit us  Follow @abbvie onX,Facebook,Instagram,You Tube,Linked Inand Tik  Tok.

Company

Description

Abb Vie’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 Abb Vie, please visit us  Follow @abbvie onX,Facebook,Instagram,You Tube,Linked Inand Tik  Tok.

Job Description

The Software Engineer will  serve as a technical expert independently designing, implementing, and optimizing system integrations for Quality systems andGxP-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

    GxPsystems, 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.
  • Optimizeandmaintaininterfaces/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, andprovidingtechnical guidance during audits or inspections.
  • Identify and implement process improvements, automation, andnew technologiessupporting integration reliability and compliance.
  • Facilitatevendor engagement for integration solutions, review contracts, gather cost estimates, and ensure partner compliance with Abb Vie'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 Abb Vie policies,GxPguidance, cybersecurity, and software development lifecycle (SDLC) standards.
Qualifications
  • Bachelors Degree with 5years experience;

    Masters Degree with 4years experience
  • At least 5 years' experience in IT or software engineering, with specific experience inGxP/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.
  • Demonstratedexpertisein 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,…
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