RhyGaze AG is seeking a hands-on Regulatory Operations professional to establish core RegOps processes, lead major submissions, and manage internal platforms. The Associate Director will implement Veeva RIM Basics, lead document management, and collaborate with Regulatory Affairs, Clinical, CMC, QA, and vendors.
The ideal candidate has 8+ years in Regulatory Operations, strong ICH/eCTD knowledge, and a track record of global submissions.
#J-18808-LjbffrRegulatory Operations Lead — Biotech Submissions in pa at Unknown Company
This position is listed as full time and onsite.