Your responsibilities * Maintain compliance with GMP requirements and applicable quality regulations across manufacturing processes and finished products. * Review, develop and update SOPs, work instructions and quality documentation, ensuring these are followed consistently in daily operations. * Assess production and batch documentation for accuracy and compliance, taking appropriate action when products do not meet release requirements. * Investigate quality incidents and deviations, work with relevant departments to identify root causes, and ensure corrective and preventive actions are implemented effectively. * Manage customer complaints, oversee investigations and coordinate the implementation of appropriate CAPAs. * Plan and perform internal audits, document findings and ensure agreed improvements are completed. * Coordinate external audits and inspections by customers and regulatory authorities, including preparation, responses and follow-up activities. * Compile annual product quality reviews,



assess quality system performance and prepare required reports and management information. * Support quality-related discussions with internal teams and external partners, including the preparation and review of quality agreements. * Advise production teams on quality requirements, promote GMP awareness and encourage a strong quality culture throughout the organization. * Identify opportunities to improve Quality Assurance processes, monitor relevant KPIs and contribute to departmental performance reporting. Your profile * A bachelor’s or master’s degree in a relevant scientific or technical discipline. * At least five years of Quality Assurance experience / GMP-regulated environment in pharma / biotech * Practical knowledge of GMP requirements, audit processes, deviation management and CAPA system #J-18808-Ljbffr

📌 Quality Assurance GMP Italy (Verona)
🏢 Resourcing Life Science
📍 Verona