Head Of Site Automation Engineering

CSL Behring

Not specified; not specified; benefits available
10+ years biopharma engineering experience
Cgmp and fda regulatory compliance knowledge
Manufacturing execution systems (mes) management
The Head of Automation Engineering provides strategic leadership to ensure the reliable and compliant operation of manufacturing execution systems and automation platforms within a global biopharma environment

Job Summary

  • The Head of Automation Engineering provides strategic leadership to ensure the reliable and compliant operation of manufacturing execution systems and automation platforms within a global biopharma environment.
  • This role is responsible for overseeing the validation, lifecycle management, and deployment of automation standards while supporting capital investment projects aligned with enterprise goals.
  • CSL Behring fosters a culture of inclusion and belonging, emphasizing values such as innovation, integrity, and superior performance to support its mission of saving lives through biotherapeutics.

Matching Summary

The Head of Automation Engineering provides strategic leadership to ensure the reliable and compliant operation of manufacturing execution systems and automation platforms within a global biopharma environment.

Salary

Not specified; Not specified; Benefits available

Skills & Requirements

Must-have

  • 10+ years biopharma engineering experience
  • cGMP and FDA regulatory compliance knowledge
  • Manufacturing Execution Systems (MES) management
  • Capital investment project leadership
  • Process control and automation expertise

Nice-to-have

  • Strategic thinking and proactive problem-solving
  • Cross-functional team collaboration skills
  • Experience with global standard deployment
  • Strong coaching and developmental focus
  • Innovation in emerging technologies

Key Requirements

  • Minimum B.S. in Engineering
  • 10+ years experience in Biopharma engineering or operations
  • Proven experience in process control and automation
  • Deep understanding of cGMPs and FDA regulations
  • Ability to lead cross-functional teams

Work Rights

Not specified

Tailored Resume

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