MDM - (Master data Management)
hace 1 mes
Note : This is a generic role don't go through the job description
Major Accountabilities:
- Ensures, defines and governs consistent master data throughout the whole master data life cycle and global business processes and defines the matrix of responsibilities within the MD process and the person that defines the parameter, the person who updates SAP with the right value, etc -Ensures that local material master data integrity and quality is established by analyzing basic requirements, maintaining the attributes in the systems and assuring all data introduced in the system is reliable and comes from the correct sources and challenges data consistency and completeness and verifies, correct and completes requests for data maintenance complying with Global Master Data processes and related SOPs.
- Identifies areas for improvement regarding Global Material Master processes, tools and rules and supports improvement processes.
- Responsible for specific Master Data Management processes (expertise, key account) to build, extend and share knowledge within self-directed working teams.
- Train and support the assigned functional SPoCs and Subject Matter Experts on site and ensure compliance with GMP and regulatory requirements (including record management) and continuous improvement of quality relevant processes within area of responsibility.
- Ensures permanent data quality and assists in data base cleaning.
- Ensure material availability in line with the approved production plan.
- Ensure daily MRP oversight for all BOM material, analysis of requirements and Purchase Orders management.
- Ensure management of daily MRP exception messages & appropriate follow up.
- Own, in ERP System, MRP relevant data and materials technical specifications and ensure no Purchase Orders are past due in the ERP System.
- Management of purchased item Complaints/Returns to supplier.
- Provide a load -balanced dispatch list for incoming materials to the warehouse and Quality department that ensures these activities are completed in line with the production needs.
- Control and follow-up of supplier’s service level indicators: Quality OTIF, lead-time violation.
- Lead action plans to achieve supplier delivery performance targets and drive for continuous improvement.
- Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)
Regards,
Mohammed Ilyas,
You can reach me through email - Mohammed@Vtekis. com
Additional Information
All your information will be kept confidential according to EEO guidelines.
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