Regulatory Affairs Specialist presso Kerr Corporation
About
More than 3 year experience working in the dental device field as Regulatory Affairs and Quality Assurance with Product/Project Management responsibilities. Most prominently:
- Work closely with compliance and post-marketing activities in accordance with MDD 93/42;
- TF management of class I through to class IIb medical devices;
- Execute registration inside and outside the EU area, in collaboration with the U.S. RA Team when/if required. Most prominently EE, EMEA, ASIA
- Lead or Support the planning, preparation (including authoring where relevant) and delivery of both simple and complex submissions throughout the product's life cycle from an EU regional perspective to act as a key p...
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