Assistant Manager of Quality

Role: Quality Manager overseeing compliance and quality systems within a plasma or biopharma manufacturing center. Objectives include maintaining inspection readiness, ensuring adherence to GMP/SOPs, and managing quality assurance processes. Responsibilities: lead site quality control activities, manage calibrations and KPIs, conduct audits, lead investigations of deviations, and ensure remediation through CAPAs. Also responsible for staff development, performance management, and fostering a culture of quality and safety; lead external audits and facilitate regulatory compliance. Requirements: Bachelor's in life sciences or related field; 5+ years in quality/regulatory roles within plasma or biopharma sectors; demonstrated leadership and supervisory experience; strong knowledge of GMP, regulations, and industry standards. HighValue: plasma/biopharma quality assurance, regulatory audits, deviation investigations, CAPA management, GMP compliance, team leadership, and regulatory interaction. WorkSetup: not specified, but likely on-site at a manufacturing or processing center.