18.04.24 | Vollzeit | Frankfurt am Main | IBM Deutschland GmbHSolid knowledge of and practical experience in SAP Basis Security, Configuration, Architecture, Authentication, Roles, Authorization, Security Governance, Vulnerability Management, Threat Management and DevSecOps - Practical experience with the following technologies/modules SAP EXX, S4 for Security
Später ansehen18.04.24 | Vollzeit | Köln | IBM Deutschland GmbHSolid knowledge of and practical experience in SAP Basis Security, Configuration, Architecture, Authentication, Roles, Authorization, Security Governance, Vulnerability Management, Threat Management and DevSecOps - Practical experience with the following technologies/modules SAP EXX, S4 for Security
Später ansehen18.04.24 | Vollzeit | München | IBM Deutschland GmbHSolid knowledge of and practical experience in SAP Basis Security, Configuration, Architecture, Authentication, Roles, Authorization, Security Governance, Vulnerability Management, Threat Management and DevSecOps - Practical experience with the following technologies/modules SAP EXX, S4 for Security
Später ansehen11.04.24 | Vollzeit | Dortmund | DNV SE MaritimeElements of DNV's Maritime Training and Authorization Scheme (MTAS) Personal qualities • Ability to work flexibly, result-oriented and self-organized • Customer-oriented approach • Enjoy working in the field as a surveyor together with a good team and operational planning • Demonstrated initiative
Später ansehen14.04.24 | Vollzeit | Bremen | Advanced Resource ManagersExpectations, and facilitating the approval of regulatory submissions. Prepare quality sections for Marketing Authorisation Applications (MAA), Biologics License Application/New Drug Application (BLA/NDA), Investigational Medicinal Product Dossier (IMPD), and Investigational New Drug (IND). Conduct gap
Später ansehen14.04.24 | Vollzeit | Düsseldorf | Advanced Resource ManagersAnd facilitating the approval of regulatory submissions. Prepare quality sections for Marketing Authorisation Applications (MAA), Biologics License Application/New Drug Application (BLA/NDA), Investigational Medicinal Product Dossier (IMPD), and Investigational New Drug (IND). Conduct gap analyses of client
Später ansehen14.04.24 | Vollzeit | Stuttgart | Advanced Resource ManagersAnd facilitating the approval of regulatory submissions. Prepare quality sections for Marketing Authorisation Applications (MAA), Biologics License Application/New Drug Application (BLA/NDA), Investigational Medicinal Product Dossier (IMPD), and Investigational New Drug (IND). Conduct gap analyses of client
Später ansehen16.04.24 | Vollzeit | München | Daiichi Sankyo Europe GmbHRegulatory requirements, internal guidelines and Standard Operating Procedures (SOPs) - Ensure timely and accurate completion of AI/ML deliverables - Contribute, with limited supervision, to documents submitted to regulatory or pricing authorities - Proactively identifies and manages risks in assigned
Später ansehen18.04.24 | Vollzeit | Mannheim | Boehringer IngelheimAnd the ability to lead without authority, we invite you to join our team and contribute to the development and launch of new products in Animal Health. Tasks & responsibilities As project leader, you will be responsible for fast and efficient technical development projects resulting in create a robust product
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