Director, IT Applications
Company: Sumitomo Pharma
Location: Marlborough
Posted on: April 2, 2026
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Job Description:
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
https://www.us.sumitomo-pharma.com 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
organization’s operational efficiency, compliance, and
effectiveness. Key Responsibilities Strategic Leadership & Roadmap
Define and own the SAP S/4HANA functional and solution roadmap
aligned with the company’s digital transformation strategy and
business goals in the pharmaceutical sector. Serve as the primary
solution architect and functional expert for 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 projects from 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 to GXP, FDA, and other regulatory requirements
applicable 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
robust SAP 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
experience in 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 a
highly 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 Bachelor’s or
Master’s 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. The base salary
range for this role is $186,880 to $233,600. 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.
Keywords: Sumitomo Pharma, Leominster , Director, IT Applications, IT / Software / Systems , Marlborough, Massachusetts