As a Process Engineer, you will support the design, scale-up, and optimisation of biologics manufacturing processes within a GMP environment. You will play a key role in improving upstream and downstream processes (USP/DSP) to enhance yield, efficiency, and robustness, while analysing process data to drive continuous improvement initiatives. You will provide technical support to manufacturing operations, troubleshoot process deviations, and implement corrective actions in collaboration with production, MSAT, and quality teams. The role also involves preparing and reviewing GMP documentation, including SOPs and batch records, while ensuring compliance with regulatory standards (EMA/FDA). Additionally, you will support technology transfer activities from development to commercial manufacturing, contribute to process validation, and work cross-functionally with QA, CQV, and engineering teams to ensure efficient and compliant operations.