Associate Director, Automation Controls – Pharma CDMO

Management Recruiters International, Inc.

Spokane (WA)

On-site

USD 180,000 - 230,000

Full time

6 days ago
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Benefits offered by this job

Full benefits from day 1
Generous relocation package
Annual bonus 15%

Job summary

Our client is a global BioPharma CDMO seeking an Associate Director of Automation Controls Engineering in Spokane, WA. The role leads a 6-person controls team, overseeing Rockwell PLCs/HMIs and OT systems, with relocation and a strong compensation package.

You will drive strategy, compliance with CFR 21 Part 11, and data integrity across manufacturing facilities, while partnering with QA, Validation, and Manufacturing to enable scalable operations.

Qualifications

  • Bachelor's degree in a technical field.
  • 10+ years engineering experience in the pharmaceutical industry.
  • 5+ years designing manufacturing controls systems, automation and capital project execution.
  • Proven leadership experience managing engineering teams and programs.
  • Ability to work in a fast-paced Pharma CDMO environment.

Responsibilities

  • Lead Controls Engineering with strategic oversight of OT systems (PLCs, HMIs, SCADA, historians).
  • Oversee capital and expense projects, ensuring on-time, on-budget delivery.
  • Ensure regulatory compliance (FDA, cGMP, EU, GAMP5) and data integrity.
  • Drive uptime, efficiency, and process improvements through IT/OT collaboration.
  • Support audits, deviations, and investigations related to control systems.

Skills

Bachelor's degree
Engineering experience
Controls design
Leadership
CDMO experience

Education

Bachelor's degree in engineering or technical field
Professional Engineer - PE License

Tools

Allen-Bradley PLCs
PanelView HMIs
Rockwell/FactoryTalk
Wonderware
Historian systems

Job description

Our client is a global BioPharma CDMO seeking an Associate Director of Automation Controls Engineering in Spokane, WA. The role leads a 6-person controls team, overseeing Rockwell PLCs/HMIs and OT systems, with relocation and a strong compensation package.

You will drive strategy, compliance with CFR 21 Part 11, and data integrity across manufacturing facilities, while partnering with QA, Validation, and Manufacturing to enable scalable operations.

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