About the Job
Oleson specialises in delivering high-quality talent and solutions that enhance the capabilities and operational excellence of our global customers.
We are focused on matching the dynamic needs of Data Centre and Life Science clients with skilled professionals, thereby driving innovations and growth in these critical sectors.
Role Description:
We are seeking an experienced SAP Master Data Management (MDM) Specialist to support a global pharmaceutical manufacturing site during a critical phase of their SAP S/4HANA implementation, with a specific focus on labelling and artwork data.
This role will play a key part in ensuring the accuracy, consistency, and regulatory compliance of product master data that underpins labelling, packaging, and product release processes.
What you’ll do:
Own and maintain master data related to labelling, artwork, and packaging, ensuring alignment with regulatory and global standards.
Support data cleansing, enrichment, and migration activities tied to product and packaging hierarchies.
Collaborate with QA, Regulatory Affairs, Supply Chain, and Artwork teams to ensure data accuracy across systems.
Assist in defining data governance rules and processes specific to labelling and artwork data.
Contribute to User Acceptance Testing (UAT), helping validate master data workflows and their impact on downstream labelling and compliance.
Support the creation of training materials and digital work instructions related to master data processes.
Act as a liaison between business stakeholders and the SAP project team to ensure data requirements are fully understood and met.
The Requirements:
Hands-on experience with SAP Quality Management (QM) in a support, consultant, or superuser capacity.
Strong hands-on experience with SAP Master Data Management (MDM) in a manufacturing or supply chain context.
Demonstrable experience managing or supporting data related to product labelling, packaging components, and/or artwork.
Knowledge of S/4HANA master data structures (materials, BOMs, classification, document info records, etc.).
Experience working in regulated environments (e.g. pharma, medical devices, biotech) with high compliance requirements.
