Global Automation Lead

CSL BEHRING

Multiple Locations
Gxp manufacturing and laboratory digital systems
Operational technology (ot) strategy and roadmap
Enterprise ot platform lifecycle ownership
The Global Head of Digital Manufacturing and Quality Control is accountable for defining and executing the enterprise strategy for GxP manufacturing and laboratory digital systems

Job Summary

  • The Global Head of Digital Manufacturing and Quality Control is accountable for defining and executing the enterprise strategy for GxP manufacturing and laboratory digital systems.
  • This role provides global lifecycle ownership, governance, and standards for platforms, data, and recipes across manufacturing and QC laboratories, ensuring harmonized, compliant, and future-ready operations.
  • CSL Behring is a global biotherapeutics leader driven by our promise to save lives, focused on serving patients’ needs by using the latest technologies.

Matching Summary

The Global Head of Digital Manufacturing and Quality Control is accountable for defining and executing the enterprise strategy for GxP manufacturing and laboratory digital systems.

Skills & Requirements

Must-have

  • GxP manufacturing and laboratory digital systems
  • Operational Technology (OT) strategy and roadmap
  • Enterprise OT platform lifecycle ownership
  • OT governance, compliance, and architecture
  • Tier 1 capital project delivery oversight
  • Strategic OT supplier and platform partnerships

Nice-to-have

  • Process Excellence methodology
  • Innovation and continuous improvement culture
  • Data-driven and integrated digital ecosystem
  • Customer Focus, Innovation, Integrity, Collaboration

Key Requirements

  • 15+ years work experience
  • 5+ years in execution systems, operational technology, IT and operations
  • Experience in process automation, MES and batch manufacturing industry standards
  • Direct experience designing, building, deploying automation and execution systems
  • Experience running site-based shop floor and laboratory systems globally
  • Proven track record influencing industry via publications/presentations
  • Demonstrated ability to influence at all organizational levels
  • Ability to build, mentor and grow a high performing team
  • Strong project management skills in biopharma manufacturing
  • Functional knowledge of cGMPs and FDA-regulated facilities

Work Rights

Not specified

Tailored Resume

Cover Letter