Global Automation Lead

Century Center

Global ot strategy and roadmap
Enterprise ot platform lifecycle ownership
Ot governance, compliance, and architecture
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

  • Global OT strategy and roadmap
  • Enterprise OT platform lifecycle ownership
  • OT governance, compliance, and architecture
  • Tier 1 capital project delivery
  • Strategic OT supplier partnerships
  • Cross-functional collaboration and influence

Nice-to-have

  • Innovation and emerging OT technologies
  • Process Excellence methodology
  • Positive and equitable working environment
  • Culture of curiosity and empathy

Key Requirements

  • 15+ years work experience
  • 5+ years in execution systems, OT, IT, and operations
  • Experience in process automation, MES, and batch manufacturing
  • Direct experience designing, building, deploying automation systems
  • Experience running site-based shop floor and lab systems globally
  • Proven track record influencing operational technology
  • 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