Senior Director, Supply Chain and Manufacturing Alliance Management

Senior Director, Supply Chain and Manufacturing Alliance Management

Hybrid - Boston Area

Damora Therapeutics is an innovative biotechnology company that aims to fundamentally redefine care for people with hematologic disorders. We are advancing a new generation of biologics to treat mutant calreticulin-driven myeloproliferative neoplasms, including essential thrombocythemia and myelofibrosis, where there is significant medical need for new disease-modifying treatments. With multiple programs with best-in-class potential on track to enter clinical development in 2026, our goal is to rapidly bring forward optimized treatments with broad mutation coverage and exceptional convenience to dramatically improve patient outcomes.

This is a unique opportunity to join a science-driven company at a formative stage, where early clinical data will directly shape development strategy and drive long-term value. The right candidate will join a team with significant early- and late-stage development experience, with the goal of quickly moving through dose escalation/expansion into pivotal trials.

The Senior Director, Supply Chain and Manufacturing Alliance Management
, will be responsible for overseeing and ensuring the seamless execution of supply chain operations and manufacturing collaborations for Damora. This role encompasses the strategic and operational leadership required for technical transfer, process validation, clinical supply management, and launch preparation. The incumbent will additionally act as the primary point of contact for financial forecasting, and contractual matters while supporting product lifecycle and regulatory readiness.

• Serve as the single point of contact for all analytical, manufacturing, warehousing, and supply chain collaborations.
• Oversee execution of signed contracts, ensuring adherence to timelines, budgets, and resource allocation for all analytical, manufacturing, warehousing, and supply chain CDMOs.
• Provide 24‑month manufacturing forecasts with monthly progress updates on collaborative activities.
• Address and elevate manufacturing or quality issues proactively, driving resolution with our collaborations.
• Maintain a structured gap assessment to track changes in manufacturing processes and analytical testing for proactive management.
• Manage and maintain financial forecast for Technical Operations.

• Lead short- and mid‑term forecasting of clinical demand and supply.
• Collaborate with Clinical Operations and external suppliers/CMOs to maintain adequate inventory levels and prevent supply disruptions.
• Implement or enhance tools to maintain up‑to‑date demand and supply tracking, working with Clinical Operations to keep sufficient clinical supply.
• Monitor and coordinate release activities across supply‑chain stakeholders, including Drug Substance (DS), Drug Product (DP), labeling and packaging (L&P), and testing entities.
• Manage the inventory and shipment logistics of all Damora product and associated samples.
• Provide recommendations on packaging design and distribution. Plan and manage execution of initial supplies and resupplies for assigned studies, designing strategic plans to supply study drug to complex global clinical trials using sound supply‑chain techniques.
• Act as IRT System Lead, supporting vendor selection activities and providing input into user‑requirement specifications of IRT management module(s).
• Review IRT strategy to ensure it supports the strategic supply plans and that IRT settings are adjusted to optimize the supply chain.
• Leverage the inventory‑management capabilities of the IRT to manage studies appropriately.
• Establish and lead ES&OP cycles to ensure launch readiness and standardize reporting for marketing and commercial teams.

• Bachelor’s degree in science, engineering, or another relevant field; advanced degree preferred.
• 15+ years of experience in supply chain and manufacturing within the biotech/pharma industry.
• Proven track record in alliance management and supply‑chain management.
• Experience in regulatory submissions, BLA preparation, and post‑approval launch activities.
• Strong…