Basel, Switzerland
Internship Explorer
Internship Explorer
As an Intern within our team in Basel, you will gain insight into the work of Technical Regulatory Affairs professionals who are responsible for providing the regulatory input and leadership for quality-related aspects of pharmaceuticals. The activities span the whole lifecycle of the product, from clinical trials all the way to the maintenance of products at the end of their lifecycle. During the internship, what will you do: * Support regulatory professionals, driving innovative regulatory strategies and produce high-quality CMC dossiers in agile and digital space * Operate as a member of global, self-managed squad teams, aligning with the organization's agile implementation. * Gain practical experience by working on various quality-related regulatory activities across the whole development lifecycle from clinical trial applications through to license applications and maintenance * Contribute to operational and business excellence aspects of regulatory, including document management, data/insights generation and business systems to advance digital and data solutions. * Work on genuine, impactful projects, providing real added value by assisting teams with their daily tasks and progressively taking ownership of defined individual projects.
