The Associate Director, Regulatory Affairs Devices and Combination Products works with internal and external partners to deliver products to patients, supporting regulatory objectives for the companyβs development and marketed device/combination products, including coordination and management of device global submissions. This position focuses on eye care devices and next generational eye care medicinal delivery products.
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USD/year
This role supports data mapping of eCTD metadata from our legacy publishing system into our future state system and supporting activities in preparation of enabling eCTD 4.0 submissions. The project work will mostly be conducted in Excel, working against data extracts from Veeva Vault RIM and requires a deep understanding of eCTD structure, metadata and organization as well as experience with Veeva Vault RIM.