SAP Consultant

2 days ago

Mundelein, United States Bayforce Full time

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.


Responsibilities

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

  • Bachelor’s Degree in Computer Science or related
  • At least 7 years total SAP systems experience and ECC manufacturing solutions
  • Strong functional and business knowledge 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

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