Executive Director, CMC Development – Technical Operations

Jasper Therapeutics

. Serve as CMC Program Leader for assigned clinical-stage development programs .

Posted 9/21/2026full-timeRemote • United StatesLead💰 $290,000 - $300,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in CMC program leadership, integrating technical operations and product development strategies into actionable plans. Proficient in coordinating cross-functional teams to ensure clinical readiness and timely supply chain management for clinical trials.

Highest-signal resume keywords

CMC Program LeadershipAnalytical Development SupportClinical Supply Chain CoordinationDrug Product ManufacturingRegulatory Affairs Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

CMC Development PlansTechnical Operations StrategyDrug Substance DevelopmentDrug Product DevelopmentClinical Trial Management

Soft Skills

Hands-On LeadershipProblem SolvingCross-Functional Collaboration

Industry Keywords

CDMOCROQuality ControlPhase 2 Clinical ProgramDevice/Combination Product

About the role

Key responsibilities & impact

Serve as CMC Program Leader for assigned clinical-stage development programs
Translate Technical Operations and product-development strategy into integrated CMC development plans and execute them successfully
Provide hands-on leadership for designated programs
Support Analytical Development and Quality Control (AD/QC) across the Jasper product portfolio
Lead technical activities conducted through CDMOs and CROs
Partner with Supply Chain, Device/Combination Product, Quality, Regulatory Affairs, Clinical Operations, and Project Management to ensure CMC readiness for clinical development
Serve as primary point of contact for all CMC activities supporting the ongoing Phase 2 clinical program in China
Plan and execute local/regional clinical drug supply and device activities
Coordinate with Clinical Operations, Supply Chain, and external partners to ensure timely clinical supply availability
Support drug product manufacturing, release, packaging/labeling, shipment, inventory, and expiry management for local clinical trials
Identify and resolve CMC and supply-related issues affecting clinical trial timelines
Support device and combination-product activities for assigned clinical programs
Serve as KP701 CMC Program Lead
Translate clinical and regulatory objectives into executable CMC activities, milestones, timelines, budgets, and deliverables
Oversee drug substance and drug product development and manufacturing

Requirements

What you’ll need

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