SAP EWM Configuration Analyst

Role Title: SAP EWM Configuration Analyst Employment Type: Contract Contract Duration: 6-month rolling contract; the overall project extends for 18 months. Preferred Location: Mundelein, IL (Onsite work required from Tuesday to Thursday) Role Description: We are looking for an SAP EWM Configuration Analyst. They need experience in SAP MM, PP, IM, and APO, with an emphasis on the EWM and IM module. Contribute to the SAP S/4 Manufacturing Product team responsible for the Plan to Produce process, including MM, PP and EWM modules. Activities include leading the operational support, enhancements, and release management of the S/4 Manufacturing systems Understand business processes in Manufacturing, Supply chain and related areas Support, architect, design and help with requirements elicitation in EWM and IM modules within SAP S/4 and ECC systems Contribute to best practices in architecting, designing & supporting S/4 PP and MM and ECC SCM applications Collaboration on projects with end-users & team members Gather and document functional/business requirements from users & sponsors Author & communicate business process design (BPD), business systems design (BSD) and system test plans Schedule & perform BSD walk-through with development team and end users Support the development of team members during detailed design & coding phase String & system integration test execution Rollout & Production support Requirements: Bachelors Degree in Computer Science or related At least 7 years total SAP systems experience with SAP EWM & IM, MM, PP and APO experience. Experience with SQL or other Data Analytical tools a plus Basic knowledge of EDI functions and use Strong integration point knowledge with APO, SD, LO and FI modules Must have a strong knowledge of discreet, process, and repetitive manufacturing processes, preferably in the medical device/healthcare industry. Experienced with labelling software such as OpenText Document Presentment Previous development experience a plus Strong communication skills - both written and verbal Experience with FDA, global trade compliance practices and import procedures a plus Must be self-motivated with capability to work independently Availability for 10-15% travel