Under minimal supervision, this position is responsible for performing activities related to process and equipment validation, corrective and preventative action reporting, internal and external audits, and supervising daily, ongoing activities related to allograft labeling, documentation review, and QC inspections of processed HCT/Ps. This position requires attention to detail and must be performed in accordance with current Regenative Labs Standard Operating Procedures (SOPs), as well as all Food and Drug Administration (FDA), American Association of Tissue Banks (AATB), International Organization of Standardization (ISO) 13485, and other regulatory agencies as necessary. This position reports to the Director of Quality Management and is responsible for communicating effectivel