The Sterile Compounding Coordinator is accountable for leadership and oversight of the health care system's sterile compounding program across all assigned locations, cleanrooms, shifts, and applicable service lines. The role leads the quality management system for compounded sterile preparations, promotes safe and reliable medication preparation, and ensures sustained compliance with organizational, regulatory, and accreditation requirements. The coordinator directs operational standards for IV-room workflow, cleanroom practices, environmental monitoring, training and competency, technology, documentation, and quality assurance in accordance with USP <797>, USP <800>, Missouri Board of Pharmacy requirements, The Joint Commission, other applicable accrediting bodies, and organizational policy. The coordinator serves as the department's subject matter expert and provides functional direction to pharmacists and pharmacy technicians engaged in sterile compounding. The role collaborates with Pharmacy leadership, Quality, Infection Prevention, Facilities, Environmental Services, Occupational Health, Nursing, Information Technology, and other stakeholders to advance safety, performance, and continuous regulatory readiness.
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Job Type
Full-time
Career Level
Senior