Need - SAP PP-QM Architect | Indianapolis, IN | Onsite | 12 months | C2C

As a Principal Consultant, required to have thorough knowledge of Manufacturing operations and Quality management along with integration with other modules e.g. GBT, MM, WM, EWM, SD, EHS and clinical trials.

Will be part of a team working on multiple projects like EWM implementation, manufacturing expansion, supporting S4 Hana landscape, working on several enhancements/Innovation items in PP, QM and other SCM areas.

Involved in impact assessment (for S/4HANA conversion), simplification Items review, requirement gathering, configuration adjustment, development support and testing, cut-over planning, deployment and hyper-care support.

Responsible to contribute as part of a team on project processes, deliverables, proposal development and client trainings as per project/organization needs.

Guide/mentor/lead the team for successful project deliveries.

Responsible for reviewing solutions designed by the team members and proposing improvements.

Responsible for liaising with client business teams and advising the client.

Dealing with customer on day to day basis and win customer confidence.

Should have 20 + years of experience in SCM area with majority of the experience in consulting experience in Manufacturing operations and quality management modules.

Should have at least 5+ end to end implementation projects experience where you have performed a role of solution architect or subject matter expert at client location.

Should have experience in all the project categories including greenfield, bluefield, upgrade, conversions etc.

Must have through knowledge in following QM areas: QM Master Data, Quality Planning, Inspection process, Notifications, Supplier Quality Management, Test Equipment Management, Batch Management.

Strong SAP PP/MO SME with knowledge of PI Sheets, Process Order Management, MES integration, BoM/Recipe Management and integration with QM and EWM, Variant Configuration, Object Dependencies

Thorough Knowledge in integration with other modules like EWM,TM, GBT, MM, WM, CO and SD

Good understanding of business processes in the life sciences / pharmaceutical domain.

Ability to understand business requirements from business users and prepare/review requirement document, functional specifications, solution design, Project estimations.

Good understanding of GXP and SOX requirements.

Should have working experience in a highly regulated environment.

Should be aware of release governance processes and have experience in working on any incident management and test execution tool.

Handled post go live critical issue resolving till stabilization