Enterprise Implementation Lead

CSL Ltd

Multiple Locations
On-site
Enterprise-wide technical implementation
Validation of horizon 2 program
Yield enhancing manufacturing technology
CSL Ltd is seeking an Enterprise Implementation Lead for its Horizon 2 program, a key role focused on the technical implementation and validation of innovative manufacturing technologies in the biopharma sector. The ideal candidate will have extensive experience in drug development and manufacturing, along with strong leadership skills to manage cross-functional teams

Job Summary

  • The Enterprise Implementation Lead is accountable for the end-to-end technical delivery of the Horizon 2 program across development, process implementation, technology transfer, validation, and the creation of development and technical content required to support global regulatory filings.
  • Partner with Manufacturing on Operational Readiness by providing Tech Ops inputs including process knowledge, tech transfer requirements, validation status, and process risk transparency.
  • Lead a lean, senior Tech Ops-focused implementation and validation team (direct and matrixed).

Matching Summary

Match Score: 85

CSL Ltd is seeking an Enterprise Implementation Lead for its Horizon 2 program, a key role focused on the technical implementation and validation of innovative manufacturing technologies in the biopharma sector. The ideal candidate will have extensive experience in drug development and manufacturing, along with strong leadership skills to manage cross-functional teams.

Skills & Requirements

Must-have

  • enterprise-wide technical implementation
  • validation of Horizon 2 program
  • yield enhancing manufacturing technology
  • high immunoglobulin production
  • enterprise integrator across Tech Ops
  • regulatory-facing technical content

Nice-to-have

  • enterprise learning and reuse
  • continuous improvement across deployments
  • collaboration across global sites

Key Requirements

  • Bachelor’s degree in a scientific or engineering discipline
  • 15+ years of professional experience in biopharma/biotech/life sciences
  • experience in drug development, manufacturing, technical transfer, Validation, CMC regulatory processes
  • full-scale MS&T support of GMP manufacturing facilities
  • Demonstrated leadership of enterprise-scale programs spanning multiple sites and capital projects
  • Proven ability to lead in complex, matrixed, global organizations

Work Rights

Not specified

Tailored Resume

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