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Supply Chain and Master Data Analyst II

Teva Pharmaceuticals
Full-time
Remote friendly (Edison, NJ)
United States
Operations

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Role Summary

Supply Chain and Master Data Analyst II. Maintains and manages material and production master data, updating master data and monitoring changes through ERP/MES/MDG systems. Establishes procedures to ensure accuracy of master data and provides support as an ERP, MDG or MES system expert. Requires understanding of pharmaceutical regulatory requirements and end-to-end pharmaceutical production processes.

Responsibilities

  • Maintain work areas and perform job functions safely in accordance with cGMPs, SOPs and batch record instructions.
  • Complete training requirements and maintain 100% compliance with assignments.
  • Create new material masters and initiate changes to material masters in the ERP system.
  • Create and revise BOM, Recipe and Production Version in the ERP system; maintain Packaging Master Record for Finished Goods; coordinate with MES for manufacturing records and packaging masters.
  • Create tests and maintain the MBR in MES; coordinate with ERP for manufacturing records and packaging masters.
  • Initiate TrackWise change controls and manage them through their lifecycle to ensure on-time closure.
  • Coordinate master data creation with MS&T to align with project timelines.
  • Coordinate with Supply Chain Planning to ensure master data readiness to support production schedules.
  • Write/revise SOPs and Work Instructions to support master data processes and requirements.
  • Cross-train and support MDG, MES and ERP as needed.
  • Provide technical support to operations for MES execution as required.
  • Provide end user training for ERP, MDG and/or MES as needed.
  • Possibly serve as a business process owner for SAP Master Data Management and/or MES.
  • Perform additional duties such as running reports and analyses to support TLMS system and team KPIs.

Qualifications

Your experience and qualifications

Any equivalent combination of education, training, and/or experience will be considered.

Education/Certification/Experience

  • Bachelorβ€šΓ„Γ΄s degree required; Supply Chain or related field.
  • Minimum 4 years of experience within a pharmaceutical or related manufacturing facility.
  • Working knowledge of QAD and TrackWise; familiarity with Glorya, SAP, MDG and MES preferred.
  • Working knowledge of master data concepts and end-to-end material flow; basic Supply Chain principles preferred.

Skills

  • Proficient in Microsoft Excel, Access, Word and Outlook.
  • Strong ability to organize resources and set priorities.
  • Ability to make administrative and procedural decisions; strong written communication skills.
  • Ability to analyze reports and make recommendations to support production demand.

Problem Solving

  • Work on problems of moderate scope, analyzing data and factors to determine solutions.
  • Exercise judgment within defined practices and select methods for resolution.
  • Typically receive little to moderate instruction and general guidance on new assignments.
  • Proactively recommend methods and procedures for problem resolution.
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