22.04.24 | Vollzeit | Trier | JT International Germany GmbHQMS objectives deployment Implement QMS framework activities and manage QMS revision, drive the revision process together with authors and coordinate pillar collaboration QMS enhancement and administration Sustain and continuously improve the overall QMS framework in alignment with relevant QA teams
Später ansehen26.04.24 | Vollzeit | Mainz | BioNTech SEAnd publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead development of statistical analysis plans and TLFs, perform statistical analyses and validate analysis results Participate in planning for health authority meetings, development of associated documents
Später ansehen25.04.24 | Vollzeit | Mainz | BioNTech SELead development of statistical analysis plans and TLFs, perform statistical analyses and validate analysis results Participate in planning for health authority meetings, development of associated documents, and the preparation of associated responses Oversee outsourced statistical CRO activities
Später ansehen25.04.24 | Vollzeit | Mainz | BioNTech SELead development of statistical analysis plans and TLFs, perform statistical analyses and validate analysis results Participate in planning for health authority meetings, development of associated documents, and the preparation of associated responses Oversee outsourced statistical CRO activities
Später ansehen24.04.24 | Vollzeit | Mainz | BioNTech SEAnd publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead development of statistical analysis plans and TLFs, perform statistical analyses and validate analysis results Participate in planning for health authority meetings, development of associated documents
Später ansehen20.04.24 | Vollzeit | Mainz | SCHOTT Pharma AG & Co. KGaAProcesses and services to improve our regulatory contribution to our business - Collaborate closely with local agents and Competent Authorities to coordinate and execute measures for product registrations. - Serve as the go-to advisor and trainer for internal SCHOTT-Pharma-specific regulatory topics
Später ansehen19.04.24 | Vollzeit | Ingelheim am Rhein | aktiv personal-service GmbHOn prioritization and possible actions for own executives and partly independent answering of requests according to instructions. - Deadline management for the executive with own decision-making authority. - Meeting management - understanding meetings (not commercial content) and writing minutes, following up
Später ansehen18.04.24 | Vollzeit | Ingelheim am Rhein | JobLeads GmbH | 100.000 € - 125.000 € For Development, Market Authorization, and the GRA Compliance and vendor oversight groups. - Responsible for harmonizing internal priorities across various functions and incorporating external regulatory and scientific trends to determine and prioritize the enhancement of regulatory affairs capabilities within
Später ansehen04.04.24 | Vollzeit | Trier | JT International Germany GmbHObjectives deployment Implement QMS framework activities and manage QMS revision, drive the revision process together with authors and coordinate pillar collaboration - QMS enhancement and administration Sustain and continuously improve the overall QMS framework in alignment with relevant QA teams
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