The people of Memorial Sloan Kettering Cancer Center (MSK) are united by a singular mission: ending cancer for life. Our specialized care teams provide personalized, compassionate, expert care to patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it. MSK is dedicated to training the next generation of scientists and clinicians, who go on to pursue our mission at MSK and around the globe. One of the world’s most respected comprehensive centers devoted exclusively to cancer, we have been recognized as one of the top two cancer hospitals in the country by U.S. News & World Report for more than 30 years.

Pay Range: $23.03-$34.67

Company Overview:
The people of Memorial Sloan Kettering Cancer Center (MSK) are united by a singular mission: ending cancer for life. Our specialized care teams provide personalized, compassionate, expert care to patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it. MSK is dedicated to training the next generation of scientists and clinicians, who go on to pursue our mission at MSK and around the globe.

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Job Description:
Quality Control Laboratory Technician, CTCEF

The QC Technician will perform the necessary testing to enable the release of cell therapy products manufactured at the Cell Therapy Cell Engineering Facility (CTCEF). Additionally, the role involves monitoring cell therapy products in patient samples post-treatment. The QC team collaborates closely with several internal and external teams to ensure the reception and processing of QC samples.

Role Overview:
· Perform various assays: Cellular (e.g. Viability, flow cytometry, cytotoxicity, cell growth-based assays), Molecular (e.g. DNA extraction, PCR, Southern Blot, QPCR, ddPCR), Biochemical (e.g. endotoxin, mycoplasma, ELISA).
· Ensure all sample testing is completed promptly, meeting both Release and Quality timelines.
· Provide immediate notification of abnormal test results and assay failures.
· Prepare all QC sample Material Transfer Document forms as needed for delivery to in-house and third-party labs.
· Provide support during the patient infusion process.
· Prepare the necessary paperwork as per cGMP guidelines.
· Assist with writing and revising standard operating procedures (SOPs).
· Contribute to writing deviation and non-compliance investigations.
· Assist with the validation process and assay improvements.

Key Qualifications:
· 1-2 years of laboratory experience or a master's degree is required. Hands-on experience in molecular biology techniques such as QPCR, PCR, DNA extraction, and cell culture is essential.
· Experience in a clinical laboratory or a controlled therapeutic manufacturing environment is highly preferred.
· The ability to work proactively and independently, and to follow through on tasks and projects.
· Action-oriented and eager to take on new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.
· Advanced skills in Microsoft Office software (Word, Excel, PowerPoint, Outlook) and relevant office applications.

Core Skills:
· Excellent communication skills and the ability to interact confidently and professionally at all levels.
· Flexibility to adapt to new projects as required to support the group.
· Adept at planning and prioritizing work to meet commitments with a keen eye for detail.

Additional Information:
· Location: 417 E 68th

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