Teva Pharmaceuticals is looking to solve the problem of maintaining and managing material and production master data to ensure consistency and accuracy, which is a foundational business enabler.
Requirements
- Working knowledge of QAD and TrackWise; Glorya, SAP, MDG and MES preferred.
- Proficient in Microsoft Excel, Access, Word and Outlook.
- Has a working knowledge of theories, practices and procedures as it relates to master data
- Working knowledge of end-to-end material flow and basic Supply Chain principles preferred.
- Knowledge of pharmaceutical regulatory requirements
- Basic understanding of the end to end pharmaceutical production process, including packaging and distribution to the distribution center(s)
- Experience with ERP, MDG and/or MES systems
Responsibilities
- Create new material masters and initiate changes to materials masters throughout the material lifecycle in the ERP system.
- Create and revise the Bill of Material (BOM), Recipe and Production Version (PV) in the ERP system.
- Creates tests and maintains the MBR in the Manufacturing Execution System.
- Initiate TrackWise change controls (CCs) and/or complete TrackWise CC tasks as assigned as it relates to the creation and maintenance of master data.
- Work with MS&T to coordinate master data creation to align with project timelines and needs.
- Work with Supply Chain Planning to ensure master data readiness to support the production schedule.
- Writes/revises procedures (SOPs and Work Instructions) to support business process and technical requirements of maintaining master data.
Other
- A minimum Bachelor’s degree required; Supply Chain or industry related fields.
- A minimum 4 years of experience within pharmaceutical or related manufacturing facility.
- Good interpersonal, organizational, and communication skills (both oral and written)
- Ability to make administrative/procedural decisions and judgments
- Ability to create, compose, and edit written materials
