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Director, GMP Shared Resource, Sloan Kettering Institute of MSK

Job in New York, New York County, New York, 10261, USA
Listing for: The American Society for Cell Biology
Full Time position
Listed on 2026-09-01
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 200000 - 320000 USD Yearly USD 200000.00 320000.00 YEAR
Job Description & How to Apply Below
Position: Director, GMP Shared Resource, Sloan Kettering Institute of MSK.
Location: New York

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 Final date to receive 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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