What are the responsibilities and job description for the GRA CMC Combination and Stand Alone Specialist position at CSL Behring?
The Lead, Global Regulatory Affairs Device is responsible for: Partnering closely with R&D, Manufacturing, Operations, Quality, and Regulatory Affairs stakeholders to address regulatory strategy challenges and deliver innovative, timely regulatory solutions that meet evolving device regulatory and compliance requirements for plasmapheresis devices, drug device combination products, standalone drug delivery devices, and ancillary devices.Ensure worldwide regulatory device compliance and successf