Manager Regulatory Affairs CMC Authoring Mainz Vollzeit BioNTech AG … for a healthy future in many people's lives. Manager Regulatory Affairs CMC Authoring You will author global quality regulatory documents and provide … a healthy future in many people's lives. Manager Regulatory Affairs CMC Authoring You will author global quality regulatory documents and provide input into … hope for a healthy future in many people's lives. Manager Regulatory Affairs CMC Authoring You will author global quality regulatory documents and …Regulatory Affairs CmcProcess Validation Engineer (f/m/d) Singen (Hohentwiel) Vollzeit Takeda Pharmaceutical … and direct collaborative projects with other VBU functions for example CMC, External Manufacturing, PO, Quality and External Partners CMOs to … of validation/technical shared services projects in support of VBU Authoring process validation documentation for Lifecycle Process Validation … Align manufacturing processes with executed validation Participate in regulatory inspections and author, review filing, submission documents Identify …Regulatory Authoring StellenangeboteAssociate Director Regulatory Affairs Aachen Home Office PAION Pharma GmbH … Affairs is responsible for establishing and implementing the regulatory CMC strategy for PAION in cooperation with other relevant functions (locally … This person ensures the update of the CMC dossier in a timely manner by authoring and reviewing relevant M1, M2 and M3 documentation. In addition, the job … Your tasks The Associate Director Regulatory Affairs is responsible for establishing and implementing the regulatory CMC …Manager Cmc Authoring Stellenangebote