SAP EWM Configuration Analyst We are seeking an experienced SAP EWM Configuration Analyst to join our SAP S/4 Manufacturing Product team. The ideal candidate will have expertise in SAP MM, PP, IM, and APO, with a strong emphasis on the EWM and IM modules. Role Responsibilities Contribute to the Plan-to-Produce process, including MM, PP, and EWM modules within SAP S/4 Manufacturing systems. Lead operational support, system enhancements, and release management for SAP S/4 Manufacturing systems. Understand and support business processes in Manufacturing, Supply Chain, and related areas. Architect, design, and elicit requirements for EWM and IM modules in SAP S/4 and ECC systems. Promote best practices in the architecture, design, and support of S/4 PP, MM, and ECC SCM applications. Collaborate on projects with end users and cross-functional team members. Gather and document functional and business requirements from stakeholders. Author and communicate Business Process Designs (BPD), Business Systems Designs (BSD), and system test plans. Conduct BSD walkthroughs with development teams and end users. Provide support to development team members during detailed design and coding phases. Perform string and system integration testing. Support system rollouts and provide production support. Qualifications Required Bachelor’s degree in Computer Science or a related field. Minimum of 7 years of experience with SAP systems, including ECC manufacturing solutions. Hands-on experience with SAP S/4 HANA and strong functional knowledge of EWM , IM , MM , PP , and APO modules. Solid understanding of integration points with APO, SD, LO, and FI modules. Knowledge of discrete, process, and repetitive manufacturing processes, ideally within the medical device or healthcare industries. Strong communication skills, both written and verbal. Self-motivated and capable of working independently. Availability for 10–15% travel. Preferred Experience with SQL or other data analytics tools. Basic knowledge of EDI functions and applications. Familiarity with labeling software, such as OpenText Document Presentment. Prior development experience. Knowledge of FDA regulations, global trade compliance practices, and import procedures.
