Director, Global Automation Engineering

AbbVie

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Chicago, IL
Salary
$182,000–$346,000 / yr
Posted
31 days ago
Freshness
Confirmed live yesterday
Closes
Aug 11, 2126

Market check

Salary context

Above market

How this pay compares to similar roles

Similar $228k
This role $264k
$152k most similar roles pay here $367k

This role pays more than 72% of similar roles. Most pay $184,500–$272,360 — the shaded band above. At the midpoint, this role pays about $264k versus about $228k 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 297 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 271 roles with salary data.

Most-posted roles

View all roles at AbbVie

At a glance

TL;DR · Director, Global Automation Engineering

Director, Global Automation Engineering serves as the enterprise-wide authority for automation architecture, process control systems, and digital infrastructure across a global manufacturing network. This leader manages a large capital project portfolio, overseeing the development of the Factory of the Future vision while ensuring all technical decisions align with regulatory requirements and industry best practices. Day-to-day responsibilities include defining automation standards, managing vendor relationships, governing site modernization programs, and leading a distributed team of engineers. The role requires expertise in Distributed Control Systems (DCS), Programmable Logic Controllers (PLC), batch automation, SCADA, OSI-PI data historians, Environmental Monitoring Systems (EMS), and Building Automation Systems (BAS). Candidates must navigate complex pharmaceutical manufacturing environments, ensuring compliance with GxP, 21 CFR Part 11, and OT cybersecurity protocols to solve challenges related to data integrity and large-scale digital transformation in the biopharmaceutical sector.

What you'll do

  • Define and execute the global "Factory of the Future" automation strategy across all manufacturing sites.
  • Serve as the primary Design Authority for automation architecture, process control systems, and digital infrastructure.
  • Manage a $100 million annual operating budget and oversee a $3 billion multi-year capital project portfolio.
  • Oversee vendor selection, qualification, and performance management for system integrators and engineering contractors.
  • Ensure all automated systems comply with GxP regulations, data integrity standards, and cybersecurity protocols.
  • Lead the development of enterprise-wide automation standards, technical specifications, and training programs.
  • Manage a high-performing, globally distributed team of automation and capital project engineers.
  • Drive the integration of automation systems with manufacturing execution (MES) and cloud-based data platforms.

What we're looking for

  • Bachelor's degree in Electrical Engineering, Chemical Engineering, Computer Science, or a related engineering or scientific discipline is required.
  • Master's degree or equivalent advanced qualification in a relevant engineering or technical field is preferred.
  • Minimum 20 years of progressive experience in automation engineering with a track record of increasing leadership responsibility across enterprise-scale organizations.
  • Significant experience within the biopharmaceutical or pharmaceutical manufacturing industry is required; experience spanning both biologics and small molecule environments is strongly preferred.
  • Proven experience leading automation scope on large-scale capital projects exceeding $50 million in an owner-side or engineering leadership capacity.
  • Extensive hands-on and leadership experience with DCS, PLC, batch automation, SCADA, OSI-PI, EMS, BAS, and related process control technologies.
  • Deep knowledge of GxP regulatory requirements, data integrity frameworks (21 CFR Part 11, EU Annex 11), and CQV practices in pharmaceutical manufacturing.
  • Demonstrated experience in OT cybersecurity strategy and enterprise-wide implementation within regulated manufacturing environments.

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