08.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHAnd represent CSPV in cross-functional meetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R
Später ansehen08.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHAnd represent CSPV in cross-functional meetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R
Später ansehen08.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHAnd represent CSPV in cross-functional meetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R
Später ansehen08.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHAnd represent CSPV in cross-functional meetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R
Später ansehen08.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHAnd represent CSPV in cross-functional meetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R
Später ansehen08.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHAnd represent CSPV in cross-functional meetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R
Später ansehen08.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHAnd represent CSPV in cross-functional meetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R
Später ansehen08.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHAnd represent CSPV in cross-functional meetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R
Später ansehen08.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHAnd represent CSPV in cross-functional meetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R
Später ansehenVerpassen Sie nie wieder einen passenden Job!
Alle Jobs für Regulatory Affairs Manager in Rosenheim kostenlos abonnieren.