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We are seeking an experienced SAP Data Architect Supplier Master for a 1 year remote contract! Lead the design, governance, and optimization of supplier master data within a highly regulated pharmaceutical environment.

This role is critical in ensuring supplier data integrity, compliance, and traceability across global manufacturing, quality, procurement, and finance operations. You will play a key role in supporting regulatory requirements, audit readiness, and SAP transformation initiatives.

Key Responsibilities

• Own the Supplier/Vendor Master Data architecture within SAP S/4HANA and/or SAP ECC
• Design and govern supplier master data models aligned to pharmaceutical regulatory standards
• Lead implementation and optimization of SAP MDG for supplier governance
• Ensure compliance with GxP, data integrity (ALCOA+), and audit requirements
• Support validated system environments and computer system validation (CSV)
• Drive supplier data harmonization across manufacturing sites, CMOs, and global entities
• Partner with Quality, Regulatory Affairs, Supply Chain, and Procurement stakeholders
• Support SAP transformation, S/4HANA migration, and integration with platforms such as SAP Ariba

Required experience:

• Proven experience as an SAP Data Architect or SAP MDG Lead within the pharmaceutical, biotech, or life sciences sector
• Deep expertise in Supplier/Vendor Master data structures in regulated environments

Strong understanding of:

• GxP requirements
• Data Integrity principles (ALCOA+)
• Audit and inspection readiness
• Segregation of Duties (SoD) and compliance controls
• Experience supporting validated SAP environments
• Strong knowledge of procurement, quality, and finance integration points
• Experience working in global, multi-site pharmaceutical organizations
• Experience supporting regulatory inspections (e.g., FDA, EMA)
• Familiarity with serialization, batch traceability, and supplier qualification processes
• Experience with SAP migration programs in validated environments
• Knowledge of industry standards such as ISO and GMP
• Supplier Master experience

Please attach your CV in WORD format to get started!

Referentie
CR/132906_1772467102

Date
2 mrt. 2026