Life Science Work · By profession

Regulatory affairs jobs in Switzerland

Regulatory affairs prepares the submissions that get a medicine or a medical device approved, and keeps it approved: with Swissmedic, the EMA and the FDA for medicines, and with notified bodies under the EU MDR and IVDR for devices. These are the open roles in Switzerland, in pharma, biotech and medtech.

Drug discovery and preclinical Clinical development Clinical operations Regulatory affairs Quality (QA and QC) Manufacturing and MSAT Process and equipment engineering Analytical development Bioinformatics and data science Medical affairs Pharmacovigilance Medtech R&D Supply chain and logistics Market access and HEOR Business development and alliance