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VP, Global Manufacturing and Supply Chain

Structure Therapeutics
August 30, 2026
Remote friendly (South San Francisco, CA)
United States
Operations
Position Summary
Vice President, Global Manufacturing & Supply Chain to lead end-to-end manufacturing, supply chain, and commercial readiness activities.

Key Responsibilities
External Manufacturing
- Develop and lead external manufacturing strategy across DS, DP, and packaged/finished product to support global clinical trials and commercial supply.
- Establish external manufacturing team, governance, KPIs, working agreements, and business review cadence; monitor execution and performance.
- Ensure manufacturing execution to meet PDUFA, launch, and ongoing supply needs (campaign planning, batch release, issue resolution).
- Lead CDMO governance and relationship management (executive interactions, KPIs, escalation).
- Accountable for CDMO performance: quality, timelines, cost, and compliance.
- Partner with Quality and Regulatory for GMP compliance and inspection readiness.
- Collaborate with CMC Development, Quality, Supply Chain, and Regulatory on technical transfers, validation strategies, and lifecycle management.
- Identify risks and implement mitigation plans.
- Provide input into make/buy, site selection, and future-state network design.
- Lead CDMO sourcing/selection (needs definition through RFP, selection, and start-up).

Global Supply Chain and Commercial Readiness
- Oversee global clinical trial material supply.
- Direct demand forecasting, supply planning, and inventory strategies for clinical/commercial needs.
- Contribute to global launch strategies and lead commercial launch execution within Tech Ops.
- Ensure capacity planning, tech transfer, and commercial-scale readiness with Technical Operations and Quality.
- Select/implement planning and performance/risk monitoring tools.
- Oversee global logistics/distribution, 3PL selection/oversight, serialization/anticounterfeiting, and global trade compliance.
- Interim global PM support as the company grows (timelines and key activities).

Qualifications
- Bachelor’s degree in supply chain, Engineering, or related field (MBA preferred).
- 20+ years progressive leadership in biopharmaceutical manufacturing/supply chain/technical operations; 5+ years in external CDMO management.
- Proven success building/scaling manufacturing & supply chain teams; leading new product launches.
- Deep understanding of GMP, GDP, Regulatory CMC expectations, and global supply chain requirements; U.S./EU launch readiness.
- Experience with small molecule API manufacturing, oral solid dosage forms, and combination products.
- Strong business acumen; strategic thinking and execution under tight timelines/budgets.
- Excellent leadership, communication, and cross-functional influence; partnership mindset.

Travel Required: Up to 30%

Application Instructions
Apply through the official career page at BambooHR.