Director, Supply Chain

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Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. With several marketed products in the U.S., Canada, and Europe, a diverse pipeline of early- to late-stage assets, and in-house advanced technology capabilities, 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 (https://c212.net/c/link/?t=0&l=en&o=4190475-1&h=3440496098&u=https://www.us.sumitomo-pharma.com/&a=https://www.us.sumitomo-pharma.com ) or follow us on LinkedIn (https://c212.net/c/link/?t=0&l=en&o=4190475-1&h=2504638834&u=https://www.linkedin.com/company/sumitomo-pharma-america/&a=LinkedIn) .

Job Overview

We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Director, Supply Chain. This position will have three key and complimentary responsibilities:

• Commercial Supply Chain strategic planning and supplier oversight.
• Lead in the design, implementation, and utilization of systems and processes to support the Supply Chain organization (planning software, ERP, visualization, reporting, master data, data analytics).
• Support for commercialization of clinical product candidates.
  
  

Job Duties And Responsibilities

• Responsible for all aspects of supply management inclusive of planning, sourcing, logistics and supplier relations in support of commercial products.
• Oversee and approve financial commitments (work orders, purchase orders, etc.) and legal contracts (Manufacturing Service Agreements, etc.) pursuant to company’s delegation of authority matrix.
• Project management of multiple initiatives related to supply chain management, with focus on systems and processes that support Supply Chain organization (planning software, ERP utilization, product strategy, Logistics, etc.).
• Work closely with R&D (Clinical Operations, Clinical Development, Regulatory Affairs), CMC, Commercial and Quality with focus on supporting commercialization of clinical product candidates.
• Oversee management of suppliers including contract manufacturing; ensure activities are performed per the approved supply agreement.
• Support the Sales & Operations Planning process to ensure coordinated efforts among groups participating in the S&OP process.
• Pursue/develop cost efficient supply chain systems and processes.
• Support the evaluation of potential suppliers and make appropriate recommendations to management.
• Support global business initiatives for supply chain as required. Lead cross-functional teams in the management of critical suppliers.
• Maintain market intelligence related to areas of responsibility and maintain streamlined and well-understood business processes and systems.
• Lead internal efforts to implement best practices throughout the supply and distribution organization.
• Implement data analytics allowing for robust decision making and inputs into various governance forums.
• Oversee strategic face-to-face business meetings with contract manufacturing partners.
• Perform in-depth, complex analysis to evaluate supply chain initiatives. Evaluate current processes or tools and recommend improvements. Generate business case analysis for supply chain projects.
• Ensure activities and operations are performed compliantly and within budget.
  
  

Key Core Competencies

• Significant experience in supply chain and distribution management in pharmaceutical or other FDA regulated environment.
• Deep understanding of regulatory and technical influences and ability to assess business and financial implications of decisions.
• Strong ability to interact with suppliers, internal customers and upper management in a professional manner.
• Strong knowledge of GMP manufacturing, quality assurance, regulatory affairs, budget planning, financials and clinical operations for biological and small molecule pharmaceuticals.
• Demonstrated ability to lead process improvement activities; delivering business processes and/or technical solutions that satisfy multiple sets of stakeholders.
• Knowledge of and interest in supply chain optimization and simulation.
• High degree of organizational awareness, ability to connect the dots to understand all the interdependency and big picture.
  
  

Education And Experience

• Bachelor’s degree in a related field required.
• Minimum 10 – 15 years (w/o Masters) or 8 – 12 years (with Master’s) of relevant experience in biotech or pharmaceutical industry.
• Ability to build a collaborative relationship with SMP and other key global partners.
• Experience in strategic global supply chain and supplier relationship management.
• Ability to manage regulatory and technical changes and assess business and financial implications of decisions.
• Strong negotiation skills and demonstrated competence to interact with suppliers, external and internal customers.
• Financial acumen and budgeting experience.
• Effective influencing and communication skills.
  
  

The base salary range for this role is $182,200 to $227,800. 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.

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.

Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. With several marketed products in the U.S., Canada, and Europe, a diverse pipeline of early- to late-stage assets, and in-house advanced technology capabilities, 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 (https://c212.net/c/link/?t=0&l=en&o=4190475-1&h=3440496098&u=https://www.us.sumitomo-pharma.com/&a=https://www.us.sumitomo-pharma.com ) or follow us on LinkedIn (https://c212.net/c/link/?t=0&l=en&o=4190475-1&h=2504638834&u=https://www.linkedin.com/company/sumitomo-pharma-america/&a=LinkedIn) .

At Sumitomo Pharma America, our work is guided by the Sumitomo Pharma mission, vision and values, which tie closely to our company’s cultural pillars.

Our Mission

To broadly contribute to society through value creation based on innovative research and development activities for the betterment of healthcare and fuller lives of people worldwide

Our Vision

For Longer and Healthier Lives, we unlock the future with cutting edge technology and ideas