Quality Specialist

Role: Quality Supervisor overseeing plasma center compliance and regulatory readiness. Responsibilities: monitor adherence to SOPs, ensure inspection preparedness, manage quality systems, coordinate training, oversee record reviews, lead investigations and corrective actions, maintain training materials and data integrity, and conduct internal audits to ensure compliance with cGMP, FDA, OSHA, and other regulations. Requirements: Bachelor’s/Associate degree in biological sciences or business administration preferred, with 3-5 years’ experience in plasma or related industry quality roles, including at least 1-year supervisory or regulated environment leadership. HighValue: industry-specific experience in plasma/biologics, cGMP, FDA compliance, internal audits, and quality management systems, with a focus on biologic product deviations. WorkSetup: details not specified.