Director, Global Automation Engineering

AbbVie

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Durham, NC
Salary
$182,000–$346,000 / yr
Posted
9 days ago
Freshness
Confirmed live yesterday
Closes
Sep 23, 2126

Market check

Salary context

Above market

How this pay compares to similar roles

Similar $218k
This role $264k
$147k most similar roles pay here $367k

This role pays more than 75% of similar roles. Most pay $168,215–$267,125 — the shaded band above. At the midpoint, this role pays about $264k versus about $218k 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 238 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 220 roles with salary data.

Most-posted roles

View all roles at AbbVie

At a glance

TL;DR · Director, Global Automation Engineering

The 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 oversees the development of the Factory of the Future strategy, managing large capital projects while ensuring technical designs align with GxP, cybersecurity, and data integrity requirements. The role involves governing technologies such as Distributed Control Systems (DCS), Programmable Logic Controllers (PLC), batch automation, SCADA, OSI-PI platforms, Environmental Monitoring Systems (EMS), and Building Automation Systems (BAS). Key responsibilities include managing vendor relationships, overseeing commissioning and qualification activities, and leading a distributed team of engineers. The position addresses the complex challenge of harmonizing automation standards across pharmaceutical manufacturing sites to ensure compliant, high-performing production environments while integrating systems with Manufacturing Execution Systems (MES) and cloud-based data solutions.

What you'll do

  • Define and execute the global "Factory of the Future" automation strategy for all manufacturing sites.
  • Act 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 five-year capital investment 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 requirements.
  • Lead the development of enterprise-wide automation standards, technical specifications, and training programs.
  • Manage a high-performing, distributed team of engineers through mentoring, coaching, and resource planning.
  • Drive the integration of automation systems with MES, ERP, and other cloud-based digital 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 manufacturing environments is strongly preferred.
  • Proven experience leading automation scope on large-scale capital projects ($50M+) in an owner-side or engineering leadership capacity across multiple sites.
  • 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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