17.04.24 | Vollzeit | Frankfurt am Main | Continental AGAnd reporting standards including CSRD, ESRS, EU Taxonomy, GDDL/LkSG, Corporate Governance Code (DCGK), German Commercial Code (HGB), Financial Accounting (esp. IFRS) and sustainability standards like ISSB, TCFD, GHG Protocol, GRI, etc. - Experience regarding regulations management, regulatory affairs
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehenVerpassen Sie nie wieder einen passenden Job!
Alle Jobs für Regulatory Affairs Associate in Hessen Bundesland kostenlos abonnieren.