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

Job description

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

Memorial Sloan Kettering Cancer Center (MSKCC) is seeking a Director for the GMP Shared Resource Facility. This faculty position is fully supported by the institution and provides strategic leadership and operational oversight for a shared, hoteling-based manufacturing and quality control environment. The Director is responsible for ensuring that all manufacturing suites and associated QC/analytical operations operates and are maintained in a continuous state of inspection readiness, meeting all regulatory, cGMP and institutional safety requirements while advancing operational efficiency and scientific innovation. This role requires a highly experienced leader capable of integrating cutting edge science, operational rigor, quality and compliance,within a complex shared-resource environment.

Applicants should have Ph.D. in life sciences and substantial (10+ years) GMP experience in a leadership role.

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.

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Worksite address

new york, NY, 10261, US

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.