Msat Visual Inspection Lead

Sanofi

Waterford, Ireland
Fully remote
Visual inspection (vi) program leadership
Injectable manufacturing excellence
Global harmonization of vi strategy
As the Global MSAT Visual Inspection Lead, you will be at the heart of Sanofi's injectable manufacturing excellence — driving the strategy, standardization, and innovation of visual inspection programs across a network of drug product sites

Job Summary

  • As the Global MSAT Visual Inspection Lead, you will be at the heart of Sanofi's injectable manufacturing excellence — driving the strategy, standardization, and innovation of visual inspection programs across a network of drug product sites.
  • You will lead a team of VI experts, champion cutting-edge inspection technologies and processes, and serve as the authoritative voice connecting Manufacturing Science, Analytics & Technology (MSAT) with Global Quality, Engineering, Procurement, and Business Strategy.
  • This is more than a technical leadership role — it is a platform to inspire teams, influence industry practices, and deliver meaningful impact for patients worldwide.

Matching Summary

As the Global MSAT Visual Inspection Lead, you will be at the heart of Sanofi's injectable manufacturing excellence — driving the strategy, standardization, and innovation of visual inspection programs across a network of drug product sites.

Skills & Requirements

Must-have

  • Visual Inspection (VI) program leadership
  • Injectable manufacturing excellence
  • Global harmonization of VI strategy
  • Defect classification and optimization
  • New VI line evaluation
  • Regulatory compliance and GMP

Nice-to-have

  • AI-powered biopharma company
  • Cross-functional and multicultural team leadership
  • Industry benchmarking and innovation
  • Proficiency in an additional European language

Key Requirements

  • Proven background in injectable manufacturing
  • Dedicated expertise in visual inspection
  • Track record of leadership and impact
  • Experience in transformation programs
  • Technology transfer and validation experience
  • Advanced degree in a scientific discipline
  • Deep knowledge of GMP and CMC requirements
  • Experience preparing regulatory dossiers

Work Rights

Not specified

Tailored Resume

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