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Manager, Enterprise - Tech Ops; SAP

Job in Boise, Ada County, Idaho, 83708, USA
Listing for: Sumitomo Pharma
Full Time position
Listed on 2026-01-30
Job specializations:
  • IT/Tech
    Data Analyst, Data Engineer, SAP Consultant
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Position: Manager, Enterprise Applications - Tech Ops (SAP)

Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner.

For more information on SMPA, visit our website  or follow us on Linked In.

Manager, Enterprise Applications - Tech Ops (SAP)
Job Overview

We are seeking a highly motivated and experienced SAP S/4

HANA Solution and Functional Manager to manage and drive our digital transformation across critical Technical Operations and Supply Chain processes. This pivotal role will focus on ensuring the seamless, compliant, and integrated operation of our core business processes—from Production to Delivery, Intercompany, Logistics, and Customer and Patient facing Integration scenarios.

The successful candidate will own the end-to-end design, configuration, integration, and validation of SAP S/4

HANA solutions, ensuring strict adherence to global pharmaceutical GxP and regulatory requirements. This is a challenging and rewarding opportunity for a seasoned SAP professional to make a significant impact on our operational efficiency, effectiveness, and audit readiness.

Job Duties and Responsibilities Production-to-Delivery & Core Functional Leadership
  • Process Ownership: Lead the analysis, design, configuration, and implementation of SAP S/4

    HANA solutions across the entire value chain, focusing on:
  • Order-to-Shipment (SD/LE): Sales Order processing, intercompany transactions, delivery processing, Billing and Invoicing.
  • Logistics Execution (LE): Shipment planning, transportation, and trade compliance.
  • Production Planning (PP): Integration of Production Orders with material planning and execution.
  • Extended Warehouse Management (EWM): Management of inventory and warehouse operations related to finished goods and raw materials.
  • Module Configuration: Expertly configure and customize SAP S/4

    HANA modules (SD, LE, PP, EWM) to align highly complex pharmaceutical business processes, including batch management, quality inspection, and serialization requirements.
  • Functional Design: Develop detailed functional designs, configuration documents, and technical specifications for enhancements, custom developments (e.g., RICEF objects), and complex business scenarios.
Enterprise Integration Management
  • Salesforce Integration: Design, implement, and maintain robust, compliant, and scalable integrations between SAP S/4

    HANA (Master Data and Transaction Data) and the Salesforce platform, ensuring accurate data flow for customer orders and financial reconciliation.
  • CGTO Integration: Strategically design and implement integration points between SAP S/4

    HANA and Cell and Gene Therapy Operations (CGTO) systems, ensuring full traceability and compliant transfer of data for patient-specific manufacturing and logistics processes.
  • System Architecture: Collaborate with Enterprise Architects to ensure solution design adheres to best practices for data integrity, performance, and security across the integrated landscape.
GxP Compliance, Validation & Quality Assurance
  • Validation Leadership: Actively participate in, and often lead, validation activities, including the generation of validation protocols (IQ, OQ, PQ) and execution of system validation and User Acceptance Testing (UAT) scripts.
  • Regulatory Compliance: Ensure all SAP S/4

    HANA configurations, custom code, and documentation strictly comply with pharmaceutical industry standards, including GxP (GMP, GDP) requirements, 21 CFR Part 11, and global data privacy regulations.
  • Testing Oversight: Own and drive the full testing lifecycle:
  • Participate in Unit Testing (UT) and System Integration Testing (SIT).
  • Lead and document User Acceptance Testing (UAT) with business stakeholders.
  • Collaborate with the testing team to identify, manage, and resolve defects through a formal change control process.
Leadership, Management & Support
  • Project Execution: Manage and prioritize…
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