Apsida Life Science in Melbourne is seeking a Regulatory Affairs Consultant for biologics to lead regulatory strategy and submissions within the Australian market. You will liaise with the TGA and coordinate CTD submissions, while guiding lifecycle activities and regulatory intelligence with global teams.
The role requires substantial experience in regulatory affairs for biologics, robust documentation skills, and the ability to work independently in a hybrid setup with 12+ month contract
📌 Biologics Regulatory Affairs Expert (Australia)
🏢 Apsida Life Science
📍 Australia
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