Jobs · Management · California

VP, Global Manufacturing and Supply Chain

Structure Therapeutics · South San Francisco, CA · 3 wk ago
On-siteManagement$300k–$390k/yrFull-time

Position Summary

As we continue to advance our innovative product pipeline and progress our lead obesity development program towards commercialization and launch, we are seeking a Vice President, Global Manufacturing & Supply Chain reporting to the SVP of Technical Operations to lead our end-to-end manufacturing, supply chain and commercial readiness activities.

Key Responsibilities

  • External Manufacturing

    • Develop and lead the external manufacturing strategy across DS, DP, and packaged/finished product to support global clinical trials and commercial supply.
    • Establish external manufacturing team, process, governance, KPIs, working agreements and business review cadence with partnership mindset and monitor execution and ongoing production performance.
    • Ensure reliable execution of manufacturing operations to meet PDUFA, launch, and ongoing supply needs—including campaign planning, batch release, and issue resolution.
    • Lead CDMO governance and relationship management, including executive-level interactions, KPIs, and escalation pathways.
    • Serve as the executive leader and primary point of accountability for CDMO performance, including quality, timelines, cost, and compliance.
    • Partner with Quality and Regulatory to ensure GMP compliance, inspection readiness, and alignment with global regulatory expectations.
    • Collaborate cross-functionally with CMC Development, Quality, Supply Chain, and Regulatory to align on technical transfers, validation strategies, and lifecycle management.
    • Proactively identify risks and implement mitigation plans to ensure continuity and robustness of external manufacturing operations.
    • Provide strategic input into make/buy decisions, site selection, and future-state network design.
    • Support business development and sourcing efforts related to manufacturing.
  • Global Supply Chain and Commercial Readiness

    • Oversee supply of clinical trial materials across global studies in alignment with Clinical Operations, CMC, and Regulatory teams.
    • Direct global demand forecasting, supply planning, and inventory strategies to support clinical and commercial needs.
    • Lead commercial launch execution activities within Tech Ops.
    • Ensure adequate capacity planning, tech transfer, and commercial-scale readiness in coordination with Technical Operations and Quality.
    • Select and implement the necessary planning and performance/risk monitoring tools to enhance visibility and data availability within the supply chain.
    • Oversee global logistics and distribution, 3PL selection and oversight, serialization and anticounterfeiting programs and ensure compliance with all global trade regulations.
    • Carry out an interim global PM role as Structure grows & help develop timelines and key activities.

Qualifications

  • Minimum bachelor’s degree in supply chain, Engineering, or related field (MBA preferred).

  • 20+ years of progressive leadership experience in biopharmaceutical manufacturing, supply chain, technical operations with at least 5+ years’ experience in external CDMO management.

  • Proven success in building or scaling manufacturing and supply chain teams and leading new product launches.

  • Deep understanding of GMP compliance, Regulatory CMC expectations and global supply chain requirements.

  • Experience with small molecule API manufacturing, oral solid dosage forms and combination products.

  • Deep understanding of GMP, GDP, and international regulatory requirements, with launch readiness experience in the U.S. and EU markets.

  • Excellent business acumen and demonstrated ability to think strategically and ensure excellence in execution in complex programs operation under tight timelines and budgets.

  • Excellent leadership, communication, and cross-functional collaboration skills.

  • Ability to influence internal and external stakeholders.

  • Partnership mindset and ability to build relationships with key partners in Quality, Regulatory, CMC, Technical Operations, R&D and Commercial functions.

  • Demonstrated success in building scalable teams, leading complex projects and driving accountability in matrixed organizations.

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