VP, Global Manufacturing and Supply Chain
Structure Therapeutics
June 25, 2026
Remote friendly (South San Francisco, CA)
United States
Operations
Position Summary
Vice President, Global Manufacturing & Supply Chain reporting to the SVP of Technical Operations 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 for global clinical trials and commercial supply.
- Establish external manufacturing team, process, governance, KPIs, working agreements; monitor execution and production performance.
- Ensure manufacturing execution for PDUFA, launch, and ongoing supply (campaign planning, batch release, issue resolution).
- Lead CDMO governance/relationships (executive interactions, KPIs, escalation pathways) and accountability for quality, timelines, cost, and compliance.
- Partner with Quality and Regulatory for GMP compliance, inspection readiness, and global regulatory alignment.
- Collaborate cross-functionally on technical transfers, validation strategies, and lifecycle management.
- Identify risks and implement mitigation plans; provide input into make/buy, site selection, and network design.
- Lead CDMO strategic sourcing/selection from needs definition to RFP, selection, start-up.
Global Supply Chain and Commercial Readiness
- Oversee clinical trial material supply globally.
- Direct demand forecasting, supply planning, and inventory strategies.
- Contribute to global launch strategies; lead commercial launch execution within Tech Ops.
- Ensure capacity planning, tech transfer, and commercial-scale readiness.
- Select planning/performance/risk monitoring tools; oversee logistics, 3PLs, serialization/anti-counterfeiting, and global trade compliance.
- Interim global PM as the company grows.
Qualifications
- Bachelor’s in supply chain, Engineering, or related field (MBA preferred).
- 20+ years progressive leadership in biopharmaceutical manufacturing/supply chain/technical operations; 5+ years external CDMO management.
- Proven success building/scaling teams and leading new product launches.
- Deep GMP and Regulatory CMC knowledge; global supply chain requirements.
- Experience with small molecule API, oral solid dosage forms, and combination products.
- Deep GMP/GDP and international regulatory knowledge; launch readiness in U.S. and EU.
- Excellent strategic/business acumen; leadership, communication, and cross-functional collaboration.
- Partnership mindset; ability to influence stakeholders and build scalable teams.
Travel Required: Up to 30%
Application Instructions
Apply via the official career page at BambooHR.
Vice President, Global Manufacturing & Supply Chain reporting to the SVP of Technical Operations 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 for global clinical trials and commercial supply.
- Establish external manufacturing team, process, governance, KPIs, working agreements; monitor execution and production performance.
- Ensure manufacturing execution for PDUFA, launch, and ongoing supply (campaign planning, batch release, issue resolution).
- Lead CDMO governance/relationships (executive interactions, KPIs, escalation pathways) and accountability for quality, timelines, cost, and compliance.
- Partner with Quality and Regulatory for GMP compliance, inspection readiness, and global regulatory alignment.
- Collaborate cross-functionally on technical transfers, validation strategies, and lifecycle management.
- Identify risks and implement mitigation plans; provide input into make/buy, site selection, and network design.
- Lead CDMO strategic sourcing/selection from needs definition to RFP, selection, start-up.
Global Supply Chain and Commercial Readiness
- Oversee clinical trial material supply globally.
- Direct demand forecasting, supply planning, and inventory strategies.
- Contribute to global launch strategies; lead commercial launch execution within Tech Ops.
- Ensure capacity planning, tech transfer, and commercial-scale readiness.
- Select planning/performance/risk monitoring tools; oversee logistics, 3PLs, serialization/anti-counterfeiting, and global trade compliance.
- Interim global PM as the company grows.
Qualifications
- Bachelor’s in supply chain, Engineering, or related field (MBA preferred).
- 20+ years progressive leadership in biopharmaceutical manufacturing/supply chain/technical operations; 5+ years external CDMO management.
- Proven success building/scaling teams and leading new product launches.
- Deep GMP and Regulatory CMC knowledge; global supply chain requirements.
- Experience with small molecule API, oral solid dosage forms, and combination products.
- Deep GMP/GDP and international regulatory knowledge; launch readiness in U.S. and EU.
- Excellent strategic/business acumen; leadership, communication, and cross-functional collaboration.
- Partnership mindset; ability to influence stakeholders and build scalable teams.
Travel Required: Up to 30%
Application Instructions
Apply via the official career page at BambooHR.