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Supply Chain Program Manager Jobs in Woonsocket, RI

Brownhealth

Director Pharmacy Supply Chain

Providence, RI · On-site

$130K - $172K/yr

The Director, Pharmacy Supply Chain serves as Brown University Health's (BUH) authoritative ... management, storage, distribution, diversion prevention, and 340B program optimization.

Verastem

Senior Director Supply Chain

Needham, MA · On-site

$260K - $300K/yr

The Senior Director, Supply Chain manages the relationships and activities with all Verastem's clinical and commercial contract manufacturing organizations (CMO'S) and is responsible for developing ...

Pwc

Supply Chain Execution Senior Associate

Boston, MA · On-site

$77K - $202K/yr

Industry/Sector Not Applicable Specialism Operations Management Level Senior Associate & Summary The Opportunity As a Supply Chain Execution Senior Associate, you will play a pivotal role in ...

Marathon TS

Operations Program Manager

Franklin, MA · On-site

$100K - $150K/yr

Operations Program Manager - (two roles) Marathon is seeking (two) experienced Operations Program ... In this role, you will serve as the primary liaison between operations, engineering, supply chain ...

Urgent

Pwc

Supply Chain Consulting - Relex Director

Boston, MA

$155K - $410K/yr

Industry/Sector Not Applicable Specialism Operations Management Level Director & Summary The Opportunity As a Supply Chain Consulting - Relex Director, you will lead efforts to optimize supply chain ...

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Supply Chain Program Manager information

See Woonsocket, RI salary details

$44.1K

$138K

How much do supply chain program manager jobs pay per year?

As of Aug 21, 2026, the average yearly pay for supply chain program manager in Woonsocket, RI is $130,753.00, according to ZipRecruiter salary data. Most workers in this role earn between $137,000.00 and $137,000.00 per year, depending on experience, location, and employer.

What is a supply chain program manager?

Supply Chain Program Managers are professionals responsible for overseeing and coordinating the end-to-end supply chain processes within an organization. They manage projects and programs that aim to improve the efficiency, cost-effectiveness, and reliability of sourcing, production, and distribution activities. Their role often involves working with cross-functional teams, managing supplier relationships, implementing new technologies, and ensuring that projects align with business objectives. Effective Supply Chain Program Managers help organizations optimize their operations and respond to market demands more efficiently.

What are the key skills and qualifications needed to thrive as a supply chain program manager?

To thrive as a Supply Chain Program Manager, you need expertise in supply chain operations, project management, and data analysis, typically supported by a bachelor's degree in business, supply chain management, or a related field. Familiarity with ERP systems (like SAP or Oracle), supply chain analytics tools, and project management certifications (such as PMP or Six Sigma) is often required. Strong leadership, problem-solving, and communication skills help coordinate cross-functional teams and drive continuous improvement. These skills and qualities are essential to optimize supply chain processes, reduce costs, and ensure timely delivery of products and services.

What are some common challenges supply chain program managers face when coordinating cross-functional teams?

Supply Chain Program Managers frequently encounter challenges such as aligning priorities between departments, managing communication across global teams, and addressing unexpected disruptions in the supply network. Effective collaboration is essential, as these managers must work closely with procurement, logistics, manufacturing, and IT to ensure seamless project execution. Strong organizational skills, adaptability, and proactive problem-solving are key to overcoming these hurdles and ensuring project goals are met on time and within budget.

What is the difference between Supply Chain Program Manager vs Supply Chain Analyst?

AspectSupply Chain Program ManagerSupply Chain Analyst
CredentialsBachelor's degree in supply chain, logistics, or related field; PMP or similar certificationsBachelor's degree in supply chain, logistics, or related field; often no certification required
Work EnvironmentOversees multiple projects, manages teams, collaborates with stakeholdersAnalyzes data, prepares reports, supports supply chain decision-making
Employer & Industry UsageUsed in manufacturing, retail, logistics companies for managing programsCommon in logistics, retail, manufacturing for data analysis and process improvement

The Supply Chain Program Manager focuses on overseeing complex supply chain projects and managing teams, while the Supply Chain Analyst primarily analyzes data to support supply chain decisions. Both roles require a similar educational background, but the Program Manager often holds certifications and has broader responsibilities.

What cities near Woonsocket, RI are hiring for Supply Chain Program Manager jobs?

Cities near Woonsocket, RI with the most Supply Chain Program Manager job openings:

Supply Chain Program Manager jobs near you

Manager, Global Clinical Supply Chain Planning

Takeda Pharmaceutical Company Limited

Boston, MA • On-site

Full-time

Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New

Takeda Pharmaceuticals rating

7.3

Company rating: 7.3 out of 10

Based on 71 frontline employees who took The Breakroom Quiz

69th of 86 rated pharmaceutical

Job description

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
OBJECTIVES / PURPOSE:
  • Responsible for developing end-to-end supply plan for innovative medicines in clinical development. The Manager, Planning Lead will attend clinical project meetings to gather relevant information, translating clinical trial protocol information into a study supply plan, forecast study product requirements, interacting and negotiation with key project stakeholders to provide delivery timelines and budget.
  • Maintains enterprise view of clinical supply chain connecting CMC, clinical operations, and commercial manufacturing perspectives across the development portfolio.
  • Responsible for scenario planning, clinical supply recommendations, and risk mitigation through detailed insight of supply and demand issues for assigned clinical programs.

ACCOUNTABILITIES:
  • The Manager, Planning Lead will be a primary Interface between clinical supply stakeholders, including Clinical Operations, Pharmaceutical Sciences (PS), GSQ, Clinical Supplies operations, and Quality Assurance.
  • Interfaces with Pharmaceutical Sciences group to ensure that trial supplies are appropriately supported and that appropriate stability programs are in-progress, and/or appropriate expiry dating exists.
  • Works closely with Logistics function to proactively plan, document, and facilitate global cross-border supply strategies, including requirements associated with controlled substances, compliance to global trade standards, and in-country investigational product regulatory requirements for delivery of product to final destinations.
  • Develop Operational Supply Plans for portfolio of development products both internal and acquired through external partnerships. Oversee forecast planning and inventory management of all relevant investigational medicines and comparators for portfolio, leading in matrix of SMEs spanning Takeda supply chain, Takeda pharmaceutical sciences organizations and external partners.
  • Lead operational feasibility assessment, scenario analysis and risk mitigation for new clinical protocols, representing the clinical supply chain to global PS teams and global program teams.
  • Develop and maintain detailed clinical supply models for supply scenarios which provides a study baseline against which to monitor assumptions and inventories of finished goods in ongoing clinical trials.
  • Lead establishment of enterprise approach to supply/demand modelling, risk identification, and scenario planning for clinical supply chain, lead cross functional planning teams to respond to unplanned events. Develop supply options, facilitate decision making, and communicate updated manufacturing and supply plans to all impacted stakeholders.
  • Responsible for execution of Operational Supply Plan throughout development lifecycle, identifying leading indicators of supply risk and escalating through PS Lead and GPL to course correct.
  • Liaise among Clinical Operations, Pharmaceutical Sciences, and Procurement disciplines in planning and managing appropriate levels of CTM and comparator supply in partnership with internal and external stakeholders.
  • Utilizes SmartSignals software to request packaging/labeling/distribution jobs, manage inventory, and shipments.

CORE ELEMENTS RELATED TO THIS ROLE:
  • Good communication, organizational, and team collaboration skills.
  • Must work effectively with global work associates.
  • Ability to interact effectively at high levels, between customers and suppliers, and to manage and resolve
    issues and to provide effective feedback.
  • Must be able to handle multiple projects simultaneously while maintaining high quality results.
  • Must be able to recognize potential conflict and escalate when necessary.
  • Presentation Skills- ability to give professional and concise presentations at internal and external meetings
  • Must be aware and compliant to regulations and requirements for functioning under GMP, GDP, and GCP's and Annex 6 and EU CT Directive, and DEA or local controlled-substance regulations as required.

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:
  • Degree in Engineering, Management, Pharmacy or other scientific/technical degree, or significant job-related experience.
  • 4+ years relevant Pharmaceutical Industry and/or Contract Provider experience, completion of 2-year Post-PharmD Fellowship experience in, or MBA is preferred.
  • Experience with Medical Devices a plus.
  • Basic understanding of GxP principles and/or ability to learn key GxP methodology
  • Provides input into Interactive Response Technology (IRT) design for randomization, supplying drug to depots and sites.
  • Proficiency in computer software applicable to IRT, Excel
  • MS Project or equivalent project management software is a plus
  • Contribute to process improvements
  • Ability to influence stakeholders from many technical disciplines and at many levels.
  • Ability to apply multiple lenses to analyze and represent complex interdependencies, scenarios, and tradeoffs.

Takeda Compensation and Benefits Summary
We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.
For Location:
Boston, MA
U.S. Base Salary Range:
$116,000.00 - $182,270.00
The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.
U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.
EEO Statement
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Locations
Boston, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Job Exempt
Yes
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.

What Takeda Pharmaceuticals employees say

Pay

Benefits

Hours and flexibility

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About Takeda Ventures

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Industry

Investment clubs and venture capital companies, pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

San Diego, CA, US

Social media

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