Must have Medical Device Experience within EU MDD and/or EU MDR

1. Coordinate the defined cadence of the EU MDR program work for claims with other copy review workstreams such as active CAPAs.
When executing up-dates of marketing materials, the aim is to maximize efficiency, minimize unnecessary re-work and make sure that different workstreams are not blocking each other.
2. Update global Surgical Technique Guides and promotional materials to all standards using compliant communication process
3. Lead and manage routings including STG, promotional materials and claims
4. Create and approve claims collection and substantiation and approval
5. Manage all asset edits with vendor and create proof within stated budget and timeline
6. Complete and approve associated F-S813 (Design Evaluation Form) to support EOS routing
7. Manage EOS routing and complete approval process for STGs, promotional materials and claims
8. Store and redistribute final approved assets