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
drug substance and drug product characterization
In vitro-In Vivo Correlation
Physiologically Based Biopharmaceutics Modelling
translational biopharmaceutics
quality by design principles
solid dosage form development
Nice-to-have
AI-powered biopharma company
cross-disciplinary subject matter experts
strong interest in science
organizational skills and attention to detail
good interpersonal skills
strong writing and presentation skills
Key Requirements
2 to 3 years of experience in pharmaceutical development
experience in biopharmaceutics or pharmacokinetics
Advanced level in modelling software (Simcyp)
good level in in vitro dissolution
good level in analytical methods
Pharmacist, Engineer with a Master's degree, or PhD