Master Data Governance Lead - Master Data Management, Global Supply Chain
Gilead Sciences - La Verne, CA
posted 3 days ago
About the position
Gilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Headquartered in Foster City, California, Gilead has operations in North America, Europe, Asia and Australia. Gilead's therapeutic areas of focus include cancer, HIV/AIDS, COVID-19, liver diseases and inflammation. Master Data Governance refers to the process of managing and maintaining master data in a consistent, accurate, and reliable manner across the Gilead organization. It involves establishing rules, policies, roles and workflows to ensure the quality, integrity and lifecycle management of material data. This role will be responsible for establishing the end to end linkages for master data between different process areas, and different systems.
Responsibilities
- Establish clear rules of how master data should be created, updated and managed.
- Ensure accuracy, completeness, consistency, and uniqueness of master data.
- Create Data Quality Rules, build dashboards by material types to measure the data quality.
- Build Data Dictionary at an attribute level that defines ownership of each attribute.
- Establish the attributes that should have LOV and ensure they follow data standards.
- Define roles and responsibilities for creating and approving master data records.
- Document the origin, transformation, movement and consumption of all the master data attributes.
- Integrate with data catalogs to provide contextual metadata.
- Document the process for data migration in case of a divesture/acquisition.
Requirements
- Doctorate and 5+ years of relevant experience OR
- Master's and 8+ years of relevant experience OR
- Bachelor's and 10+ years of relevant experience.
Nice-to-haves
- Experience in pharmaceutical operations/cGMP environment highly desirable.
- Experience with Data Standards and Policies, Data Quality Management, Process for Data Migration / Industry Standards.
Benefits
- Company-sponsored medical, dental, vision, and life insurance plans.
- Discretionary annual bonus.
- Discretionary stock-based long-term incentives.
- Paid time off.
