Director, GMP Shared Resource, Sloan Kettering Institute of MSK.

Responsibilities: Operational Leadership Oversee day-to-day operations of the GMP shared resource facility, including: Facility maintenance, environmental monitoring and suite readiness Equipment maintenance, qualification, and lifecycle management Raw material sourcing, qualification and inventory management Ensure manufacturing suites are appropriately configured, equipped, and compliant for all scheduled GMP activities Support technology transfer and onboarding of new processes into the facility Analytical and Quality Control Leadership (Core Function)Provide strategic and technical leadership of all QC and analytical operations, positioning the function as a central enabler of product release and regulatory compliance Establish and maintain a phase-appropriate, risk-based analytical control strategy across multiple product modalities (e.g., cell therapies, viral vectors, biologics) Oversee: Assay development, qualification, validation, and lifecycle management In-process, release, and stability testing programs Method transfer, comparability, and bridging strategies for evolving processes Ensure all analytical methods are: Scientifically rigorous and fit-for-purpose Fully compliant with cGMP and data integrity standards Scalable and adaptable to emerging technologies and product platforms Build and maintain robust analytical infrastructure and capabilities, including: Instrumentation strategy and platform standardization Reference standards and critical reagents Trending, statistical analysis, and data review systems Drive timely and compliant batch disposition by ensuring QC readiness aligns with manufacturing timelines Collaborate closely with MSK research laboratories to translate early-stage assays into GMP-compliant methods Quality and Compliance Partner with MSK’s Clinical Research Quality Assurance unit to: Maintain documentation and ensure regulatory compliance Oversee and maintain core quality systems, including deviations, CAPA, change Control and Document management. Drive continuous improvement of the Quality Management System (QMS)Ensure continuous inspection readiness and serve as the primary subject matter expert during regulatory audits and user inspections Strategic Planning and Financial Stewardship Develop long-term operational strategies aligned with institutional needs Manage infrastructure and operating budgets Establish sustainable models to support facility growth and evolving demand People Leadership Recruit, train, and mentor a multidisciplinary team Foster a high-performing, inclusive culture grounded in integrity and accountability Stakeholder Engagement Build and maintain strong, collaborative relationships across MSK, including research, clinical, and quality organizations Serve as a key liaison between GMP operations and internal and external stakeholders Communicate proactively regarding operational readiness, risks, and strategic initiatives The deadline for applications is September 15th, 2026. MSK is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects of recruiting and employment. Women and minority candidates are strongly encouraged to apply.