• Perform preparation of document packages for regulatory submissions for new and mature products to ensure alignment and compliance with local and regional registration requirements as well as with company policies from all areas of company as well as internal audits and inspections. • Compile all materials required in submissions, license renewal and annual registrations. • Prepare the necessary copies of international documents, CE Certificates, CFG's and other regulatory documents. • Assist in updating and maintaining Technical files for submission to the Notified Body for changes in manufacturing and/or design. • Maintain the Global RA database for the Corporation. • Provide administrative support to RA Department personnel. • Complete other tasks assigned by management as needed.