This position will provide support to ensure the organization maintains compliance with the organization’s Quality Systems, current Good Manufacturing Practices (cGMPs), current Good Tissue Practices (cGTPs), and in adherence with all applicable Federal, State, local, international, and industry regulations and standards. This position will also oversee the management of regulatory documentation related to the organization’s Institutional Review Board (IRB) activities. Will assist with the new and ongoing qualification of suppliers performing collections. The position works closely with QA management staff, the Medical Director, Operations Team, etc. to ensure all regulatory documents and requirements are met. This individual will perform a variety of activities needed to establish and maintain compliance; including responsibilities associated with the quality assurance tasks.