Global Automation Lead

CSL SEQIRUS

Gxp manufacturing and laboratory digital systems
Pas, mes, osi pi, and lims platforms
Global lifecycle ownership and governance
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
  • PAS, MES, OSI PI, and LIMS platforms
  • Global lifecycle ownership and governance
  • Operational Technology (OT) strategy and roadmap
  • ISA-88/95 and Pharma 4.0 principles
  • Enterprise OT platform lifecycle ownership
  • OT governance, compliance, and architecture

Nice-to-have

  • Process Excellence methodology
  • Innovation and continuous improvement
  • Data-driven and innovation-oriented ecosystem
  • Positive and equitable working environment
  • Customer Focus, Innovation, Integrity, Collaboration

Key Requirements

  • 15+ years' work experience
  • 5+ years in execution systems, OT, IT, and operations
  • Experience in process automation, MES, batch manufacturing standards
  • Direct experience designing, building, deploying automation/execution systems
  • Experience running shop floor and lab systems globally
  • Proven track record influencing industry via publications/presentations
  • Experience building, managing, deploying global systems
  • 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