Lukas Däuwel

Drive improvements of GMP production processes, workflows, and manufacturing documentation (MPRs, SOPs, forms, and work instructions) Contribute to deviation investigations, root cause analysis, CAPA development, and implementation of corrective actions Collaborate with MSAT, Engineering, QA, and Production to implement process improvements and support data-driven investigations

Coordinated shift operations and provided end-to-end process oversight in a GMP manufacturing environment Planned and optimized upstream workflows and ensured smooth process transitions Trained and onboarded production personnel in GMP-compliant manufacturing processes

Executed upstream and midstream processing using bacterial systems at 1500 L production scale Operated large-scale bioprocess equipment and performed in-process controls in a GMP environment Supported reliable and consistent execution of manufacturing processes and troubleshooting activities

Independently planned and executed upstream bioprocess development using prokaryotic expression systems Operated benchtop bioreactors and analytical equipment for process development Prepared and executed GMP-relevant batch records and process doc

Practical semester abroad at UPF Pompeu Fabra, Barcelona, in the virology department, including a final report Master thesis at AGC Heidelberg, Process Development Department: “Development of an industrial manufacturing process for in-vitro transcription related process proteins”

Practical semester at the Paul Ehrlich Institute, Langen, including a final report Bachelor thesis at Paul-Ehrlich Instuitut: "Characterization of Chikungunya escape mutants"