Lüleburgaz, Kırklareli, Türkiye
• Oversee the compliant batch release of high-potency (oncology) pharmaceutical products by reviewing manufacturing records, test results, and deviations in accordance with GMP and regulatory standards. Collaborate with cross-functional teams to resolve quality issue, and ensure timely product release. •Prepare Product Quality Review (PQR) reports to assess product performance and quality trends. •Develop and maintain In-Process Control (IPC) documents for manufacturing processes. •Conduct monthly audit trails in production areas to ensure compliance with GMP and internal quality standards. •Oversee and approve raw material transfer forms as part of quality assurance processes.