SAP Authorization Change Manager | SAP-Autorisierungs-Change Manager (w/m/d)
Siemens AG
Job Summary
Join a global IT SAP organization within a leading medical technology company, Siemens Healthineers, as an SAP Authorization Change Manager. This critical role involves taking full end-to-end responsibility for designing and successfully implementing SAP authorization concepts across SAP ECC, S4/HANA, Embedded BW, and HANA DB systems. You will be instrumental in developing and consolidating SAP system-specific roles and profiles, ensuring stable change implementation in an international setting. A core focus is maintaining IT and procurement compliance, including Segregation of Duties (SoD) and the four-eyes principle, while supporting audit activities to meet stringent security and quality requirements, particularly concerning US FDA 21 CFR regulations for medical devices. This position offers flexibility, allowing up to 60% mobile work within Germany, and requires strong expertise in SAP authorization management and regulatory compliance in a highly regulated environment.
Required Skills
Education
Master's degree in Business Informatics / Data Processing Systems, General Informatics, or Business Administration. Bachelor's degree or completed vocational training with additional professional experience is also acceptable.
Experience
- Several years of professional experience in change and requirements management
- Professional experience in SAP Authorizations Audit
- Experience with legal requirements for Non-Product Software for global medical technology products and services
- Experience in Software Validation Principles in a regulated environment
- Familiarity with ISO 27001 Controls Environment
- Familiarity with FDA 21 CFR Part 11 Electronic Records and Electronic Signatures
- Experience managing external service providers and partners
Languages
Additional
- Willingness to work mobile (within Germany) up to 60% of the time. Mobile work from selected foreign countries is possible for up to 30 days per year under specific conditions. Must ensure compliance with US FDA Article 21 regulations.
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