Automation Director – Biopharma GMP & Plant Start-Up

Meet Life Sciences

Indianapolis (IN)

On-site

USD 140,000 - 190,000

Full time

14 days+
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Job summary

A leading life sciences company is seeking an experienced Associate Director of Automation Engineering to lead and develop a team within a biologics manufacturing facility in Indianapolis. In this full-time role, you will shape automation strategies and support project delivery and compliance. Key responsibilities include overseeing automation systems, guiding team development, and managing financial performance. Qualified candidates should have over 10 years of experience in biopharma engineering and a strong background in GMP environments.

Qualifications

  • 10+ years’ experience in biopharma engineering, automation, IT, operations, or manufacturing.
  • Proven experience in automation engineering within a biologics or GMP manufacturing environment.
  • Strong people leadership experience, including coaching, performance management, and team building.

Responsibilities

  • Lead, coach, and develop a team of process control engineers.
  • Ensure reliable, compliant automation systems supporting daily biologics manufacturing operations.
  • Provide automation leadership during design and delivery of a greenfield facility.

Skills

10+ years’ experience in biopharma engineering, automation, IT, operations, or manufacturing
Proven experience in automation engineering within a biologics or GMP manufacturing environment
Strong people leadership experience
Hands-on knowledge of SCADA, DCS, and MES platforms
Experience delivering highly automated greenfield manufacturing sites

Tools

DeltaV
Rockwell
Syncade

Job description

A leading life sciences company is seeking an experienced Associate Director of Automation Engineering to lead and develop a team within a biologics manufacturing facility in Indianapolis. In this full-time role, you will shape automation strategies and support project delivery and compliance. Key responsibilities include overseeing automation systems, guiding team development, and managing financial performance. Qualified candidates should have over 10 years of experience in biopharma engineering and a strong background in GMP environments.
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