14.05.24 | Vollzeit | München | Rodenstock GmbHAn der Datenverarbeitung und SW-Tests sowie regulatorischen Aspekten für die Medizinproduktezulassung Souveräner Umgang mit MS Office Verhandlungs- und präsentationssicher in Englisch und gutes Deutsch Kommunikationsstarker, proaktiver Teamplayer mit einem analytischen und innovationsgetriebenen Arbeitsstil
Später ansehen08.05.24 | Vollzeit | Fürstenfeldbruck | 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 | Erding | 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 | Erding | 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 | Erding | 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 | Freising | 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 | Friedberg | 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 | Germering | 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
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