Raoul Hennig

Leitung des Bereichs gRNA Herstellung. Zuständig für: 5 Reinraumbereiche, 3 Herstellungs-Teams, 3 Support-Teams. Personalverantwortung >70 Tox-Studien, klinische Studien (Phase I-III), Validierung (PPQ) und kommerzielle Herstellung

Project lead of five teams (Personnel responsibility ~30) Manufacturing of APIs (planing till batch release); Process upscaling from R&D to Pilot-/ GMP-Scale; Large scale process development and -implementation cGMP: Generation of customized batch records, SOPs, Change Controls Deviation management, root cause analysis, development of effective CAPAs Representative of the API manufacturing division at GMP and SHE audits

cGMP guidlines (EU, FDA, ICH) Quality and deviation management; Change Control and CAPA; Process validation and equipment qualification; Project and time management; leadership training

Project development and manangement, process/data analysis, publication, literature research Design and supervision of bachelor and master theses, training of PhD-students Protein biochemistry, membrane biogenesis in photo-autotroph organisms, with a first author publication in nature communications.

Identification of the unknown function of an essential protein (IM30/Vipp1) in photosynthestic membrane biogensis. During the thesis research function and structure of the protein were revealed and published in several articles in international accepted journals.

Main disciplines: Molecular biology, protein biochemistry and genetics