RESPONSIBILITIES/DUTIES:
 Revise and update Quality and Regulatory documents. Manage and maintain Quality and Regulatory documents. Ensure all quality system documents meet Quality Manual and Corporate Procedure requirements. Maintain Device History Records (Finished Goods and Raw Material) subject to incoming inspection at Jacksonville Facility.
Provide support to all departments. Maintain organized filing system for the QA/RA department (CAPA, Complaints, Internal/External Audits, Management Review Meeting Minutes, Nonconforming Reports (MRB’s) and Scrap Authorization files).