Job Description

• Performing day to day activities of processing master Data tickets assigned as per the relevant SOPs , business matrix, SLA time lines & KPIs . • The primary focus of the associate is to learn & develop understanding to generate insights through data using available tools & technologies. • By analyzing the basic requirements, maintaining the attributes in the systems, and ensuring that all the data included in the system are reliable and from the right sources, ensure that the integrity and quality of site master data is established. • Basic understanding of Material Master data Process and Supply chain objects. • Basic Understanding of Pharma product and lifecycle events • High priority maintenance of data quality of master data and avoid duplication • Develop understanding of working in a GxP environment and adhere to the compliance policies of Novartis • Work in a team environment ensuring collaboration and mutual respect • Focus on innovation and bringing a fresh perspective to the traditional processes • Ensure accountability & ownership of the assigned tasks • Participate and complete all mandatory trainings assigned • Good communication skills (both written & verbal) • Responsible for setting the right priorities to ensure timely release of material codes to manufacturing sites in order to guarantee successful implementation of the products on the market. • Contribute in continuous improvement projects to achieve operational excellence Preferred candidate profile Material Master Updating, Creation of Purchase info record, Source list, Global Material/ SAP Pharma background. SHARE RESUMES TO NEDUNURI.SAIKUMAR@MANPOWER.CO.IN COMPANY : NOVARTIS ( 1 YEAR CONTRACT ROLE )

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