Senior QA Specialist - Biopharma Compliance & Validation

KBI Biopharma, Inc. is seeking a Principal QA Specialist in North Carolina to lead compliance review of GMP data, oversee QA activities across analytical and microbial labs, and support product lifecycle and regulatory inspections. The role emphasizes patient safety, regulatory adherence, and cross-functional collaboration. The position requires deep QA/QC and cGMP expertise, with extensive experience in FDA/EU regulations, method qualification, and CAPA processes.