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Director Global Supply Chain Planning

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Beam Therapeutics

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Location:
United States , Cambridge, MA / Durham, NC

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Category:
IT - Administration

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Contract Type:
Employment contract

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Salary:

210000.00 - 260000.00 USD / Year
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Job Responsibility:

  • Develop and implement supply chain analytics, planning, and resilience processes and policy across the global supply chain for all stages of the product lifecycle
  • Oversee and manage global end to end supply planning and network design as Beam transitions from clinical to commercial stage company over next few years
  • Ensures appropriate inventory, including design/policy for Raw and Critical Materials (pDNA, mRNA, gRNA, mAb, lipids), Drug Substance, Bulk Drug Product, and Finished Drug Product
  • Oversee and manage S&OP process
  • Collaborate cross-functionally with ClinOps and Program teams to ensure accurate demand forecasts and scenarios/analytics
  • Responsible for supply network analysis to support tactical and strategic decision making
  • Coordinate with Finance, Program Teams, CMC and PD to ensure robust modeling of product and network scenarios to support decision-making in governance forums
  • Perform risk-based review of supply chain in order to determine appropriate inventory levels
  • Communicate demand uncertainties or risks and develop options for optimizing supply network capacity and capabilities
  • Deliver a response plan for disruptive challenges
  • Ensure that plan and capabilities of each CDMO and suppliers are adapted to minimize the risk of disruption and deliver an effective response to ensure resilience
  • Ensure optimal economics, and adequate supply chain security in partnership with Finance for Budget, LRP and capital planning processes
  • Oversee team to develop supply chain strategies, bringing integrated solutions to the production network
  • Hire, develop and mentor staff as needed
  • Direct activities of all functions involved in planning, warehousing, logistics to ensure control of materials from the receipt of raw materials to the delivery of the finished product including inventory controls
  • Oversee and publish metrics to reflect the effectiveness and efficiency of department activities including supply chain KPIs on inventory, responsiveness and costs
  • Implement KPIs that drives accountability and improvement in both operational and financial metrics
  • Partner with NC Mfg to implement standardized site planning and scheduling processes and procedures
  • Participate in the design & implementation of SAP Phase 3 and IT roadmap in preparation for commercial launch
  • Other duties as assigned

Requirements:

  • BS/BA degree in Business, Science, Engineering or related field with 15+ years of experience in global supply chain from pharma, biotech or cell & gene therapy companies
  • Prior drug development, manufacturing, clinical operations experience is a plus
  • Master's degree or MBA preferred
  • Prior management skills with leadership experience building and sustaining global teams
  • Passion for patients, collaborative and effective leader
  • Advanced knowledge of contracts, negotiation, vendor management
  • Knowledge of practical implications of Sarbanes-Oxley controls
  • Knowledge of continuous improvement methodologies and tools
  • Strong organizational and facilitation skills, with high degree of customer focus
  • Focuses on immediate and urgent business needs while driving long term strategic plans and capability & organizational development
  • Provides strategy, vision and direction regarding issues that may have company-wide impact
  • Requires in-depth knowledge of the functional area, business strategies, and the company’s goals
  • Possesses industry-leading knowledge of sourcing direct materials
  • Expertise and track record in manufacturing and supply chain execution and oversight
  • Expert in standing up a formal S&OP process
  • Extensive experience in supply chain planning, SAP ERP system, capacity modeling, supply network strategy and optimization
  • Expertise and proven track record in supply chain risk management
  • Possesses in-depth knowledge of industry and system best practices
  • Solid knowledge of regulatory requirements, regulatory guidances, including pharmaceutical GMPs and ICH guidance
  • Current on Biopharma supply chain, manufacturing technologies, supplier network, CMO network, performance and capacity
  • Possesses understanding and application of principles, concepts, practices, and standards for DS and DP manufacturing in the biopharma industry
  • Strong communication, negotiation, and interpersonal skills
  • Strong analytical skills and ability to clearly communicate at tactical and strategic level with team and Sr Management
  • Ability to work in a dynamic and challenging environment
  • Some travel may be required
  • Must be able to work onsite, not a remote role

Nice to have:

  • Prior drug development, manufacturing, clinical operations experience is a plus
  • Master's degree or MBA preferred

Additional Information:

Job Posted:
May 20, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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