Senior Scientist Biopharm

Sanofi UK

Montpellier, France
Hybrid
Solid dosage form development
In vitro-in vivo correlation
Physiologically based biopharmaceutics modelling
The department is responsible for the development of preclinical, clinical, and commercial formulations, from their manufacturing and transfer to pilot for clinical batches, to industrial transfer and submission of the marketing authorization application

Job Summary

  • The department is responsible for the development of preclinical, clinical, and commercial formulations, from their manufacturing and transfer to pilot for clinical batches, to industrial transfer and submission of the marketing authorization application.
  • As a Manager in charge of solid dosage form development, you will ensure the design of formulation studies and process development, from laboratory to industrial scale, across all cycles related to Sanofi's product research and development.
  • Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do.

Matching Summary

The department is responsible for the development of preclinical, clinical, and commercial formulations, from their manufacturing and transfer to pilot for clinical batches, to industrial transfer and submission of the marketing authorization application.

Skills & Requirements

Must-have

  • solid dosage form development
  • in vitro-in vivo correlation
  • physiologically based biopharmaceutics modelling
  • quality by design principles
  • cross-disciplinary teams

Nice-to-have

  • AI-powered biopharma company
  • innovative pharmaceutical forms
  • stimulating scientific environment
  • digital tools transformation

Key Requirements

  • 2 to 3 years of experience
  • pharmaceutical development experience
  • biopharmaceutics or pharmacokinetics
  • modelling software (Simcyp)
  • in vitro dissolution
  • analytical methods
  • Pharmacist, Engineer with Master's, or PhD

Work Rights

Not specified

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