Find Idorsia Pharmaceuticals jobs in Switzerland.
In this role, you will provide expert support for clinical trial quality, ensure compliance with ICH-GCP and global regulatory expectations, and act as a key partner to internal teams and CROs. You will be responsible for quality oversight, process
Lead the development of new chemical entities with a focus on Drug Substance matters. Lead manufacturing and scale-up activities toward API including supplies of building blocks, Regulatory starting materials or GMP intermediates