23.03.24 | Vollzeit | Hannover | Process Automation Solutions GmbHStandards, and ensures the timely delivery of projects while maintaining quality, budget and customer satisfaction. *CoE PMO Center of Excellence Project Management Office - As a head of CoE PMO you provide strategic direction and leadership to the project management team in global PA, fostering
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
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