The Sr. QA Officer will be part of a young team which consists of driven QA professionals in a GMP environment. You will support establishing a quality system following GMP and applicable international guidelines. Moreover, activities within this role include daily interaction with other departments concerning change control, CAPA, deviation, risk assessments audit management and documentation and maintaining and evaluating quality indicators. Additionally, writing, implementing, reviewing and maintaining procedures and other QA-related documentation in alignment with applicable GxP guidelines. Identifying documents which need to be created or updated and ensuring this is organised. Moreover, you should be able to weigh the risk of the event and provide the most efficient compliant solution and contribute to improving the Quality System, implement and improve current procedures and processes such as the management of training, audits and vendors. Lastly, performing and reviewing internal and external audits, as lead auditor, to determine compliance with applicable guidelines (like GMP, GLP, GDP). You will present the QA department with significant projects.