Stellenangebote für Technical Support Jobs in Kaiserslautern Landkreis

04.06.25 | Vollzeit | Kaiserslautern | JobLeads GmbH | 40.000 € - 60.000 € Our clients worldwide and present the project results - Provide high-level technical support as well as plan and execute user trainings - Write case studies, whitepapers, project documentation, and software handbooks Your Profile - Academic education in a STEM* discipline - Experience with complex

03.06.25 | Vollzeit | Kaiserslautern | JobLeads GmbH | 40.000 € - 60.000 € Administrator experience supporting Department of Defense information systems. - Proficiency using MS Office, including Word, PowerPoint, Excel, SharePoint, Visio, and Teams. *Major certifications include CASP+, CCIE, CCISO, CCSP, CFR, CISM, CISSP, CySA+, CNP, GCED, GCFA, GCIH, GCIG, JNCIE-SEC, Google

03.06.25 | Vollzeit | Kaiserslautern | JobLeads GmbH | 60.000 € - 80.000 € And development of Modeling and Simulation (M&S) standards that support the US Air Force, Department of Defense, and mission partners facilitating all-domain Warfighter training across the full spectrum of conflict. (This position is supporting a short-term contract.) This role of this position is to support

14.03.25 | Vollzeit | Rüsselsheim | BioNTech SEEstablish means to identify and mitigate quality-related risks linked to the global core processes Enable your team to identify and execute process improvements while ensuring regulatory compliance Ensure audit and inspection readiness, provide required oversight and support for regulatory inspections

10.03.25 | Vollzeit | Rüsselsheim | BioNTech SESpecialist QA Systems Training (m/w/d) Mainz, Germany full time Job ID 8821 The Specialist QA Systems - Training supports the development of a global training program in the Veeva eQMS, aligning to One QMS initiatives. This role works cross-functionally with various sites and departments to ensure

07.03.25 | Vollzeit | Kaiserslautern | BioNTech SEScalable, secure, and aligns with clinical trial needs, supports reproducibility, and complies with regulatory standards (e.g., FDA 21 CFR Part 11, GxP) Lead the creation, and standardization of reusable macros, scripts, and automation pipelines (e.g., SAS macros, Python/R workflows) to streamline dataset

27.02.25 | Vollzeit | Kaiserslautern | BioNTech SEProcess within BioNTech. The GPO ensures alignment with business objectives, regulatory compliance, and operational excellence while driving standardization, technical innovation, and efficiency across the process. This person will also lead a team of Business Process Owners (BPOs) and collaborate