Job Details:

• 6+years with SAP
• 6+years of Project Management
• 6+ years of Business Requirements Documentation
• 6+ years with Systems Development Life Cycle (SDLC)
• 6+ yeas of Stakeholder Management
• This position will be split between SAP responsibilities and IT Plan operations for Biologic Development labs.

Detailed Description:

• Experience in gathering and documenting system requirements specifications for SAP in Manufacturing preferably in the Pharmaceutical sector.
• Provide input to and during the analysis of the "As-Is" and "To-Be" processes, specifically from local regulations and statutory requirements standpoint.
• Provide input to and during the analysis process in terms of how SAP meets local regulations and requirements.
• Ability to work with minimum supervision and under severe time constraints.
• Significant experience in the Pharmaceutical sector or in other FDA regulated industries. At lease 2 full implementation cycles in the functional area.
• Strong knowledge of Good Manufacturing Practices and local regulations.
• Experience in the implementation of the PP, MM, QM and WM Modules.
• Experience with Product Planning, Manufacturing Execution, Inventory/Warehouse Management, Bar Coding, Product Costing, and Quality Management
• Working knowledge of the SDLC
• Command of project management techniques and tools.
• Ability to work independently with minimal supervision
• Excellent written and oral communication skills
• Experience with business partner and stakeholder management
• Ability to build a strong network across business units
• Highly organized and possesses the ability to manage multiple projects and priorities at the same time.