08.04.24 | Vollzeit | Darmstadt | 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 | Darmstadt | 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 | Darmstadt | 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 | Darmstadt | 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 | Darmstadt | 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 | Darmstadt | 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 | Darmstadt | 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 | Darmstadt | 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 | Darmstadt | 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
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