Quality Control Laboratory Specialist, CTCEF

2 weeks ago

New York, New York, United States Memorial Sloan Kettering Cancer Center Full time

Compensation Range:
$23.03-$34.67

Company Overview:

At Memorial Sloan Kettering Cancer Center (MSK), our mission is clear: to eradicate cancer for good. Our dedicated teams provide tailored, compassionate, and expert care to patients of all ages.

Our scientists engage in groundbreaking translational and clinical research, driven by fundamental studies conducted at our Sloan Kettering Institute, enhancing our understanding of cancer and improving prevention, diagnosis, and treatment methods.

MSK is committed to nurturing the next generation of scientists and clinicians who will carry our mission forward both at MSK and globally.



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Job Summary:

The Quality Control Laboratory Specialist at CTCEF will conduct essential testing to facilitate the release of cell therapy products produced at the Cell Therapy Cell Engineering Facility (CTCEF).

This role also includes monitoring cell therapy products in patient samples following treatment.

The QC team works closely with various internal and external teams to ensure the proper reception and processing of QC samples.


Key Responsibilities:

  • Execute a variety of assays; Cellular (e.g., Viability, flow cytometry, cytotoxicity, cell growth assays), Molecular (e.g., DNA extraction, PCR, Southern Blot, QPCR, ddPCR), and Biochemical (e.g., endotoxin, mycoplasma, ELISA).
  • Ensure timely completion of all sample testing, adhering to both Release and Quality timelines.
  • Provide immediate notification of any abnormal test results and assay failures.
  • Prepare all necessary QC sample Material Transfer Document forms for delivery to in-house and third-party laboratories.
  • Offer support during the patient infusion process.
  • Complete the required documentation in accordance with cGMP guidelines.
  • Assist in drafting and revising standard operating procedures (SOPs).
  • Contribute to the documentation of deviations and non-compliance investigations.
  • Support the validation process and enhancements of assays.

Essential Qualifications:

  • 1-2 years of laboratory experience, with hands-on expertise in molecular biology techniques such as QPCR, PCR, DNA extraction, and cell culture being crucial.
  • Experience in a clinical laboratory or a regulated therapeutic manufacturing environment is highly preferred.
  • Ability to work independently and proactively, following through on tasks and projects.
  • Action-oriented with a readiness to embrace new opportunities and challenges with urgency, high energy, and enthusiasm.
  • Proficient in Microsoft Office applications (Word, Excel, PowerPoint, Outlook) and relevant office software.

Core Competencies:

  • Strong communication skills with the ability to interact confidently and professionally at all levels.
  • Adaptability to new projects as required to support the team.
  • Skilled in planning and prioritizing work to meet commitments with meticulous attention to detail.

Additional Information:

  • Schedule: On-site
  • Reporting to the CTCEF QC Supervisor

Hourly Compensation Range:
$23.03-$34.67

Helpful Links:
MSK Compensation Philosophy
  • Review our comprehensive benefits offerings #LI-POST MSK is an equal opportunity and affirmative action employer dedicated to diversity and inclusion in all facets of recruiting and employment.

    All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sexual orientation, national origin, age, religion, creed, disability, veteran status, or any other factor that cannot lawfully be used as a basis for an employment decision.

Federal law mandates that employers provide reasonable accommodations to qualified individuals with disabilities. Please inform us if you require a reasonable accommodation to apply for a job or to perform your job.

Examples of reasonable accommodations include modifications to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or utilizing specialized equipment.

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