Master Data Management Specialist

Amgen

(Washington, District of Columbia)
Full Time
Job Posting Details
About Amgen
Amgen is one of the world’s leading biotechnology companies. Amgen is a values-based company, deeply rooted in science and innovation to transform new ideas and discoveries into medicines for patients with serious illnesses.
Summary
The Master Data Management Specialist is responsible for managing the entry, maintenance, adherence to standard design, and accuracy of Basic Data and Quality Master Data elements which include but not limited to Commercial, Clinical, and Raw Material Masters and Material Requests in SAP
Responsibilities
1. Provide process and system guidance and training to department staff and maintain Global Master Data training material. 2. Extract, compile and interpret data relevant for periodic metrics and reporting needs. 3. Provide continued Master Data leadership in managing core data needs. 4. Upholds global master data governance process. 5. Support or manage process improvement initiatives and projects. 6. Provide business process guidance to internal clients on the workflow process 7.Apply analytical skills to evaluate and interpret complex situations/problems using multiple sources of information. 8. Participate in BPO’s global forum. 9. Test SAP functionality, support ERP releases. 10. Monitor functional area data quality reports and identify revisions to data quality reports, to proactively prevent, identify, monitor, and correct master data errors. 11. Manage change control that impacts SAP Material Master Data. 12. Owns department documentation.
Ideal Candidate
**Education/Licenses** * Doctorate degree or Master’s degree and 3 years of operations or supply chain experience or Bachelor’s degree and 5 years of operations or supply chain experience **Preferred Qualifications** * Material, Production, Planning master data and/or OA inspection plan experience * Supply chain data management experience * Understanding of database fundamentals * Master’s Degree or APICS certification * Working knowledge of regulatory and pharmaceutical processes * Solid project management, cross functional facilitation, communication and presentation skills. * Team player, self-starter, persistent, tactful, persuasive, independent worker who take on ownership in driving tasks/projects to completion * Readily adapts to and manages change * Process improvement and leadership skills focused on implementing robust, efficient systems & processes, * Analytical skills in data management, interpretation and reporting * Experience with Change Control Management system, e.g., Trackwise, * Ability to establish relationships with key stakeholders across multiple functional areas, both onsite and virtually. * Excellent organizational skills and communication skills, communicating concisely and timely with clients.

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