Regulatory Affairs Specialist

Regulatory Affairs Specialist

Raleigh client seeking contractor for onsite Regulatory Affairs Specialist, M-F. The Regulatory Affairs Specialist will be responsible for supporting regulatory activities for existing US FDA class III medical devices. This role provides support to currently-marketed products, involves evaluating proposed product and process changes, assessing documentation and providing guidance to ensure regulatory compliance. The Regulatory Affairs Specialist will :

• Support Regulatory Activities
• Evaluate Proposed Product and Process Changes
• Assess Documentation
• Provide Guidance to Ensure Regulatory Compliance