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You'll code with machine learning languages like DataBricks and Python Libraries to synthesize millions of data sets into patterns that answer ad hoc requests and then use Tableau for data visualization.
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Strong Knowledge of Data Warehouses/Lakehouse architectures, Master Data Management, Data Quality Management, Data Integration, and Data Warehouse architecture.
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Establish and maintain effective communication and collaboration with functional area peers including Pharmacovigilance, Drug Supply, Quality Assurance, Regulatory Affairs, Legal, Medical Writing, Biostatistics and Data Management to meet program objectives and support achievement of goals.
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The Specialist, Planning and Master Data will be responsible for creating, updating, and maintaining master data elements supporting Client' Cell Therapy treatment center account management.
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Our continued success is achieved through our omnichannel fluency and curated digital suite of capabilities, including Account Services, Creative, Digital and Brand Strategy, Digital Production and Project Management, 3D Animation, Digital Development, and Video.
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You will be involved in holistic surveillance build out which will require excellent understanding and hands-on experience in big data (Hadoop - Cloudera stack) technologies like hive, spark, Kafka, Angular JS to architect, develop and support sophisticated analytics pipeline using Machine Learning algorithms.
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Strong understanding of regulatory requirements and compliance issues affecting clients related to privacy and data protection, such as PCI DSS, GLBA, Basel II, EU Data Protection Directive, International Cross Border, and U.S. State Data Privacy Laws.
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Generates SOPs and Work Practices within Celgene’s Document Management System and electronic work plan template and measurement data templates to establish the Use, Maintenance and Calibration plans for GMP equipment.
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Must have 6+ years of pharma / clinical research / data management / health care experience or 8+ years of project management experience (and / or applicable work experience). Manage and maintain vendor budgets for assigned clinical trials and process flows and data exchanges with global pharmacovigilance for clinical trial serious adverse events.
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Key Responsibilities Joining a team of highly qualified materials management and supply chain professionals, this individual will be responsible for supporting the supply chain management process, systems, and software functions for MRP, ERP, data sources, testing, integrations, reporting, analytics, and more within the cell therapy network.
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Data science, machine learning, optimization models, PhD in Machine Learning, Computer Science, Information Technology, Operations Research, Statistics, Applied Mathematics, Econometrics, Successful completion of one or more assessments in Python, Spark, Scala, or R, Supervisory experience, Using open source frameworks (for example, scikit learn, tensorflow, torch.
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Intelligent Asset Management, With A Team of Leading Practitioners having deep functional & industry knowledge specializing in the area of Asset Integrity and Reliability Management, Master Data Management, EAM & Maintenance Execution, Material & MRO Management, Industry Analytics and Digital Industrial Workforce.
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In-depth knowledge and thorough experience in programming, configuring, and/or integrating using/with Azure integration tools like Data factory, LogicApps, Functions, API Management, Data catalog, WebApps, Integration service environment, configuring monitoring & diagnostics, etc., and connectivity & security configurations (certificates, encryptions, etc.
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Master Data Management: Oversight the establishment and maintenance of core master data sets to be established to support pharmaceutical lifecycle from development to commercialization partnering with related functions to ensure a building in model to support all eQMS systems and evolving Global GMP capabilities and awareness for data management and records retention.
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Experience with MES infrastructure, ALM and Veeva document/change management systems and middleware WebMethods. Provide CSV & validation Production and Project support to S12 MES Next Gen. Complete all tasks required per the Change Management Process for S12 MES Next Gen SOP and in compliance with CSV and related SOPs. Review the summary reports from testing/validation to ensure all issues are resolved and approved.
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data management warehousing jobs in Florham Park, NJ
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