Director, IT Applications

Sumitomo Pharma


Job Location:

Marlborough, NH - USA

Monthly Salary: $ 186880 - 233600
Posted on: 27 days ago
Vacancies: 1 Vacancy

Job Summary

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 womens 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 LinkedIn.

Summary

We are seeking a highly motivated and experienced Director IT Supply Chain and Quality to play a pivotal role in our ongoing digital transformation journey. Reporting to the Sr. Director of IT this leadership position will be responsible for defining the strategic direction leading the implementation and ensuring the optimal utilization of SAP S/4HANA across key pharmaceutical business functions. The ideal candidate will possess deep functional and technical expertise in the core SAP modules critical to Production Delivery Supply Chain Quality Management (QM) Manufacturing (PP/ME) Extended Warehouse Management (EWM) Intercompany and Direct Procurement (MM) within a regulated environment. This is a challenging and rewarding opportunity for a seasoned SAP professional to make a significant impact on our organizations operational efficiency compliance and effectiveness.

Key Responsibilities

Strategic Leadership & Roadmap

  • Define and own theSAP S/4HANA functional and solution roadmapaligned with the companys digital transformation strategy and business goals in the pharmaceutical sector.

  • Serve as the primarysolution architect and functional expertfor all integrated S/4HANA modules (focusing on PP MM QM SD EWM and related master data).

  • Lead the translation of complex business requirements into scalable compliant and efficient SAP S/4HANA solutions leveraging best practices fit-to-standard analysis and industry knowledge.

  • Manage a portfolio of SAP projects and enhancement initiatives ensuring alignment with budget timeline and quality standards.

Implementation & Optimization

  • Direct and govern end-to-end SAP S/4HANA implementation projectsfrom blueprinting configuration testing go-live through post-implementation support.

  • Oversee the functional design and configuration for core business processes including:

    • Procurement:Direct Intercompany and Source-to-Pay processes (MM integration).

    • Supply Chain & Manufacturing:Production planning (PP) execution (ME integration) inventory management and material requirements planning (MRP).

    • Quality & Compliance:Quality Management (QM) processes including batch management inspection plans stability studies and integration with manufacturing and logistics.

    • Warehouse & Logistics:Advanced/Embedded Warehouse Management (EWM) for a regulated warehouse environment.

  • Ensure that all SAP solutions adhere toGXP FDA and other regulatory requirementsapplicable to the pharmaceutical industry including validation and documentation standards.

Team Management & Governance

  • Lead mentor and manage a team of internal SAP functional consultants solution architects and external system integrators.

  • Establish and enforce robustSAP governance processes including change management release management and documentation standards.

  • Act as the key interface between the IT department Business Process Owners and Executive Leadership.

Qualifications

  • 10 years of progressive experiencein SAP functional and solution delivery with direct experience leading SAP S/4HANA implementation or large-scale transformation projects.

  • Deep hands-on functional expertise across multiple core SAP modules specifically:PP (Production Planning) QM (Quality Management) MM (Materials Management) and EWM (Extended Warehouse Management).

  • Demonstrated experience in ahighly regulated industry (Pharmaceutical Biotech or Medical Device) with a clear understanding of GXP validation and compliance requirements.

  • Proven track record of success in a leadership capacity managing large complex cross-functional teams and projects.

Education & Technical Skills

  • Bachelors or Masters degree in Computer Science Information Technology Engineering or a related field.

  • Strong understanding of S/4HANA architecture Fiori apps embedded analytics and modern SAP integration technologies.

  • Exceptional communication presentation and interpersonal skills with the ability to influence and align stakeholders at all levels of the organization.

** Travel requirements - up to 25%

The base salary range for this role is $186880 to $233600. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases short incentive plan participation eligibility for our 401(k) plan medical dental vision life and disability insurances and leaves provided in line with your work state. Our robust time-off policy includes flexible paid time off 11 paid holidays plus additional time off for a shut-down period during the last week of December 80 hours of paid sick time upon hire and each year thereafter. Total compensation including base salary to be offered will depend on elements unique to each candidate including candidate experience skills education and other factors permitted by law.

Disclaimer: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities duties and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time as needed.

Confidential Data:All information (written verbal electronic etc.) that an employee encounters is considered confidential.

Compliance: Achieve and maintain Compliance with all applicable regulatory legal and operational rules and procedures by ensuring that all plans and activities for and on behalf of Sumitomo Pharma America (SMPA) and affiliates are carried out with the best industry practices and the highest ethical standards.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Mental/Physical Requirements: Fast paced environment handling multiple demands. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time.

Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) employer

Qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital domestic partnership or civil union status; sex gender; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.


Required Experience:

Director

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 womens health rare diseases cell & gene therapies and CNS. With several marketed products and a diverse pipeli...

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Improving health of people everywhere - innovative treatments, science, and tech to address patient needs in oncology, urology, women's health, rare diseases, CNS, and cell & gene therapy.

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