Job Title: SAP S/4 HANA Implementation Engineer 3
2 resources needed
Location: Onsite, Sunnyvale, CA
Project Duration: 09 Months
Interview Process: Zoom Interview with In-Person Interview, Total 2 Rounds (For Non-Local can go for Zoom)
Position Requested 2 Openings
- Strictly functional candidate
- New project
- Need to be a part of project blueprint
- Strictly locals
- SAP PP S/4 HANA side (not ECC HANA side) core pp experience
- S/4 HANA New Implementation
- Interfacing Mes Tools - Experience
- PLM
- SENIOR CONSULTANT NEEDED - WHO WORKED IN REGULATED ENVIRONMENT END - END PP IMPLEMENTATION EXPERIENCE (HEAVY MANUFACTURING BACKGROUND)
- 1 - S/4 HANA IMPLEMENTATION EXPERIENCE
- MIGRATING FROM ECC HANA TO S/4 HANA
- MINIMUM 5 YEARS OF PP MODULE
- This is a Functional role, we are not looking for a Technical or Developer kind of candidates.
- Need someone who can work onsite.
- SAP PP with S/4 HANA Side of it. (New Implementation) within a Manufacturing Environment.
- Senior person who has worked on End-to-End Implementation
At least 2 to 3 implementation SAP PP
And 1 implementation on S/4 HANA
- SAP PP integrate with any MES system.
- SAP PP integrate with any PLM application.
- Worked in regulatory environment.
- SAP PPDS is not mandatory.
- Open to consider non-local consultant who's willing to relocate at their own expenses from day one.
- Minimum 10+ years of SAP experience
- - Minimum of 5 years of experience in SAP PP module with SAP S/4 HANA
- - Strong knowledge and hands-on functional configuration and design experience in standard SAP Production Planning (PP) Discrete and Repetitive Manufacturing, integrated with PLM application, MES system and SAP PPDS. Very good understanding of integration of SAP modules in End-to-end business processes
- - Experienced to Propose, Build, Configure, Integrate, Test and Document solutions meeting specific functional and technical customer requirements.
- - Good understanding of business processes in medical device industry, broad experience working with industry standards, regulations, CSV (Computer Systems Validation) and guidelines in medical device industry
- - Work closely with peers in other IT verticals such as Development and Integration, Infrastructure, Information Security and Project management office.
- - Good understanding of GXP and SOX requirements, should have working experience in a validated environment.
- - Ability to understand business requirements from business users and prepare and review functional specifications.
- - Self-motivated, Go-getter and competent to work independently.
Skills :