Engineer, Technology II

AbbVie

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Chicago, IL
Salary
$78,500–$141,000 / yr
Posted
10 days ago
Freshness
Confirmed live yesterday
Closes
Sep 21, 2126

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $155k
This role $110k
$65k most similar roles pay here $207k

This role pays less than 85% of similar roles. Most pay $131,350–$179,375 — the shaded band above. At the midpoint, this role pays about $110k versus about $155k for comparable roles.

Based on 240 similar postings.

Employer

About AbbVie

AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines and solutions in immunology, oncology, neuroscience, and eye care. Its products include Humira, Skyrizi, and Rinvoq.

AbbVie currently has 229 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 211 roles with salary data.

Most-posted roles

View all roles at AbbVie

At a glance

TL;DR · Engineer, Technology II

Engineer, Technology II serves as a technical expert within the Clinical Supply Systems group, focusing on data, reporting, and integration solutions for Clinical Supply Management. The role involves designing and deploying operational reports, metrics, and dashboards using Jaspersoft and SQL against Oracle and PostgreSQL databases. You will act as a Business System Owner, managing system health, change management, and vendor relations while engineering system-to-system integrations involving API logging and monitoring. Key responsibilities include performing root cause analysis for integration failures, managing master data quality, and driving process automation to improve efficiency. The position requires proficiency in SQL development, data warehousing concepts, and experience with platforms like Veeva Vault and Sensitech SensiWatch. This role addresses critical business needs within the GxP-regulated clinical supply chain environment to ensure seamless data flow and system reliability.

What you'll do

  • Design and deploy operational reports, dashboards, and KPI views using Jaspersoft and SQL against Oracle and PostgreSQL databases.
  • Act as the Business System Owner by managing system health, configuration, change control, and disaster recovery planning.
  • Engineer and support system-to-system integrations with external vendor platforms using API logging and monitoring mechanisms.
  • Perform root cause analysis for integration failures by correlating application logs, API responses, and database activity.
  • Manage master data quality, including item classifications and mapping, while assessing the impact of changes on downstream systems.
  • Identify and implement automation opportunities to improve efficiency within Clinical Supply Management processes.
  • Execute system lifecycle activities including technical documentation, user acceptance testing (UAT), and GxP compliance tasks.
  • Create training materials and update global standard operating procedures (SOPs) for internal users and stakeholders.

What we're looking for

  • Bachelor's degree and at least 5 years of relevant experience, or a Master's degree and at least 4 years of relevant experience.
  • Strong SQL development skills for query authoring, tuning, and troubleshooting against Oracle and PostgreSQL databases.
  • Hands-on experience developing and deploying reports in Jaspersoft/JasperReports including parameterization and distribution.
  • Understanding of relational database design, data models, and data-warehouse concepts to navigate unfamiliar schemas.
  • Experience engineering system-to-system integrations involving API/interface concepts, log analysis, and root cause investigation.
  • Ability to elicit requirements from business stakeholders and translate them into technical deliverables.
  • Demonstrated ownership of a business system including change management, access definition, and vendor coordination.
  • Familiarity with clinical supply management systems (IRTs, Signant’s PMD, Loftware’s P360, Master Control’s Mx) and Sensitech SensiWatch. (preferred)
  • Experience with scripting or automation in Python for data processing and operational tooling. (preferred)
  • Experience preparing training materials, SOPs, or work instructions and delivering system training. (preferred)
  • Prior experience in clinical drug development, clinical supply chain, or a GMP regulated environment. (preferred)
  • Experience with computer system validation, UAT, change control, and GxP documentation practices. (preferred)

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