Quality Specialist

Role: Quality Assurance Coordinator supporting plasma center compliance and operational quality. Responsibilities: perform final QA review and release of shipments, ensure accuracy and regulatory adherence of center records, manage training documentation and LMS data integrity, coordinate and monitor staff training, conduct process assessments, lead internal audits, and investigate non-conformities. Also responsible for safety policies, external audit hosting, and maintaining a compliant, safe work environment. Requirements: High school diploma; 1+ year leadership or regulated environment experience; strong organizational, decision-making, and problem-solving skills; understanding of quality systems and regulatory training standards. Preferred: Associate or Bachelor's in business or biological sciences. High-value specifics: regulated plasma collection, cGMP compliance, FDA and OSHA regulations, internal and external audits, Trackwise investigations, safety policies, and process improvement initiatives. Work setup involves standing/walking most of the time with physical requirements including lifting up to 25 lbs; occasional work with temps and odors. Collaboration mainly with center management and quality team, reporting to Assistant Manager of Quality.