A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.
Post : Assoc Mgr Data Mgmt
Job Description
The Global Associate Master Data Manager has to maintain global master data for Clinical Finished Goods by maintaining the corresponding Master Data objects (e.g. Material Master, Study master, Batch Master, Bill of Materials and Recipes) following global quality standards/processes and providing support to the Line Function- Drug Supply Management. Global Associate Master Data Manager creates and maintains worldwide unique identified materials through the whole material life cycle ( from Drug Supply Management Forecast and Demand planning to the production and distribution of Clinical Finished Goods) to be managed within Novartis SAP systems. Global Associate Master Data Manager is responsible for material uniqueness following consistency rules to ensure high quality of material defining or describing attributes. The Associate Master Data Manager should ensure Global materials data integrity and quality by analysing basic requirements of Data required for Planning and Packaging of Clinical Finished goods He / She also ensures maintenance of data related to regulatory compliance of the Clinical Finished Goods Materials.
• Creates/Maintains Global Master Data, challenges data consistency and provides support to the Line Function Users in SAP systems.
• Data/Information provider to verify/correct and complete requests for data • Identifies areas for Improvement regarding Global Master Data Processes, Tools and Rules.
• Proactively investigates to correct identified errors.
• Creates and maintains Material types related to various types of Global Studies- IRT Based, Double Blind Patient Based, Single Blind, and Open Label.
• Acts as Master Data Single Point of Contact for Clinical Finished Goods to other departments/function, e.g. PHAD, CHAD, PSP, TRD QA and Finance.
• Supports / Assists in Improvement of Materials management processes.
• Understands the product ‘life cycle’ from Development and Manufacturing to Distribution of all affected material storage/movement/billing types from/to vendors/customers
• Responsible for specific Global Master Data Management processes (expertise, key account) to build, extend and share knowledge within self directed working team.
• Build on to future capabilities in Training / On-boarding of new members in the Master Data Group -Clinical Finished Goods.
• Performs complex transactions and queries using the appropriate tools.
• Ensures high level of Data quality and assists in data base cleaning.
• Ensure GMP compliance within area of responsibility.
Candidate Profile
Experience : Min 4+ yrs exp in MDM.
Academic Qualification: Preferably Masters in Science / Diploma in Scientific / Pharmacy related background. Other qualification levels as appropriate. Knowledge: The position requires an understandin English: fluent – any additional language would be advantageous Prior experience in Data Management or related field desired. Preferred experience/knowledge in the pharmaceutical industry and/or supply chain management
Additional Information:
Experience: 4+ yrs
Industry Type: Pharma/ Healthcare/ Clinical research
Functional Area: R&D
Job ID: 233506BR
Last Date: 1st March, 2018
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