Roche
Pharmaceutical
GlobalClinicalMasterDataSpecialist
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Global Clinical Master Data Specialist at Roche. Skills: Master Data Management, SAP, GMP, GCP. Manage GMP/Quality-relevant master data lifecycle processes. Create and update Material Masters”
Industry & Context.
Troubleshooting; Root-cause analyses
What They're Looking For.
Must Have
University degree in Life Sciences, Computer Science, Business Administration, or related field, Minimum 5 years of professional experience in Master Data Management, Deep, foundational understanding of GMP and GCP guidelines, Expert-level knowledge of SAP R3P Clinical, S/4HANA, MDGM, APO, and OMP, Proficient with VEEVA platforms, Fluent in written and spoken English
Nice to Have
Background knowledge in Clinical Supply within the pharmaceutical industry, Professional proficiency in German
What You'll Do.
Manage GMP/Quality-relevant master data lifecycle processes
Create and update Material Masters
Update Classifications
Update business partner/vendor data
Oversee production-related data architectures
Maintain Master Recipes
Maintain Bills of Materials
Maintain Production Versions
Ensure data alignment across SAP R3P Clinical
Lead Engineering Change Management workflows
Coordinate Engineering Change Requests
Coordinate MDGM workflows
Act as single point of contact for master
Manage system user accounts and roles
Oversee Quality Records within VEEVA
Monitor Key Performance Indicators
How You'll Work.
Team & Collaboration
Cross-functional collaboration; Partner with Production; Partner with Supply Chain; Partner with Quality; Partner with Pharma Affiliates
Full Job Description
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. ### ### The Position A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. The mission of the Global Clinical Supply Chain Organisation (PTDS) is to ensure that no patient is left without treatment and no clinical trial is delayed. Our vision is to provide innovative and sustainable clinical supply solutions to anyone, anywhere, at any time. By joining our team, you will play a key role in advancing Roche’s diverse and robust biopharmaceuticals pipeline, encompassing over 100 molecules in approximately 500 clinical trials across seven disease areas in more than 80 countries. ## The Opportunity As our Global Clinical Master Data Specialist, you will serve as the backbone of our clinical supply chain, ensuring that global production and distribution systems run seamlessly by managing the critical data that fuels our operations. In this role, your impact and responsibilities will include: * **End-to-End Data Stewardship:** Manage GMP/Quality-relevant master data lifecycle processes, creating and updating Material Masters, Classifications, and business partner/vendor data. * **Production Data Management:** Oversee production-related data architectures, including the precise maintenance of Master Recipes, Bills of Materials (BOM), and Production Versions. * **System Integration & Synchronization:** E
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