Director, Regulatory Affairs

Veeva Systems, Inc. is seeking an experienced MedTech Regulatory Information Management consultant to lead implementations worldwide. You will guide Regulatory Affairs and Operations transformations, working with Professional Services to deliver end-to-end data and documentation workstreams. The role emphasizes cross-team collaboration, customer liaison, and building adoption roadmaps while applying industry standards such as FDA, EU MDR/IVDR, and UDI.