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 Austria (Iquitos)
🏢 Resourcing Life Science
📍 Iquitos