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Cell Therapy Quality Control Specialist
2 months ago
Pay Range:
$23.03-$34.67
Company Overview:
At Memorial Sloan Kettering Cancer Center (MSK), our team is driven by a singular mission: to eradicate cancer for life. Our dedicated care teams offer personalized, compassionate, and expert treatment to patients of all ages.
Guided by groundbreaking research from our Sloan Kettering Institute, scientists at MSK collaborate to perform innovative translational and clinical research, revolutionizing our understanding of cancer and enhancing our capabilities in prevention, diagnosis, and treatment.
MSK is committed to nurturing the next generation of scientists and clinicians who will carry forward our mission both at MSK and globally.
Please review important announcements about vaccination requirements and our upcoming EHR implementation by clicking here .Important Note for MSK Employees:
Your Career Hub profile serves as your internal resume submitted to the hiring team. Ensure your profile is complete with your skills, relevant experience, and education (if required). Click here to learn more. Please note, this link is only accessible for MSK employees.
Job Description:
Quality Control Laboratory Technician, CTCEF
The QC Technician is responsible for conducting 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 reception and processing of QC samples.
Role Overview:Conduct a variety of assays including: 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.
Promptly notify relevant parties of abnormal test results and assay failures.
Prepare all necessary QC sample Material Transfer Document forms for delivery to in-house and third-party laboratories.
Provide support during the patient infusion process.
Complete required documentation in accordance with cGMP guidelines.
Assist in writing and revising standard operating procedures (SOPs).
Contribute to the documentation of deviations and non-compliance investigations.
Aid in the validation process and improvements of assays.
Key Qualifications:
1-2 years of laboratory experience is required. Hands-on experience with molecular biology techniques such as QPCR, PCR, DNA extraction, and cell culture is essential.
Experience in a clinical laboratory or controlled therapeutic manufacturing environment is highly preferred.
The ability to work proactively and independently, while following through on tasks and projects is crucial.
Action-oriented individuals who are eager to embrace new opportunities and challenges with a sense of urgency, high energy, and enthusiasm are encouraged to apply.
Proficiency in Microsoft Office software (Word, Excel, PowerPoint, Outlook) and relevant office applications is necessary.Core Skills:
Exceptional communication skills with the ability to interact confidently and professionally at all levels.
Flexibility to adapt to new projects as needed to support the team.
Adept at planning and prioritizing work to meet commitments, with a keen attention to detail.
Additional Information:
Schedule:
On-site
Reporting to the CTCEF QC Supervisor
Hourly Range:
$23.03-$34.67
Helpful Links:
MSK Compensation Philosophy
Review our great benefits offerings
Closing:
MSK is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects 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 which cannot lawfully be used as a basis for an employment decision.
Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job.Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.
