Italfarmaco is seeking an experienced candidate in Alcobendas, Spain to author and review CMC sections for drug registration applications.¿Todo listo para enviar su solicitud? Asegúrese de comprender todas las responsabilidades y tareas asociadas a este puesto antes de continuar.The role focuses on ensuring regulatory compliance and supporting quality assessments throughout the product lifecycle.
Idóneo candidates will have at least 4 years of CMC experience, a degree in a relevant scientific discipline, and strong attention to detail. xcskxlj This position offers the opportunity to work in a dynamic environment with a focus on team collaboration and regulatory strategies.