Quality Assurance Lab Technician
2 weeks ago
Compensation Range:
$23.03-$34.67
Company Overview:
At Memorial Sloan Kettering Cancer Center (MSK), our team is driven by a shared goal: to eradicate cancer for good.
Our dedicated care teams deliver personalized, compassionate, and expert treatment to patients of all ages.Informed by groundbreaking research conducted at our Sloan Kettering Institute, scientists at MSK work collaboratively to advance innovative translational and clinical research, revolutionizing our understanding of cancer and enhancing our capabilities in prevention, diagnosis, and treatment.
MSK is committed to educating the next generation of scientists and clinicians, who will continue our mission both at MSK and globally.
Please review important announcements regarding 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 applicable). Click here to learn more. Please note, this link is only accessible for MSK employees.
Job Summary:
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 collaborates closely with various internal and external teams to ensure the effective reception and processing of QC samples.
Role Responsibilities:1. 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)
- Biochemical (e.g., endotoxin, mycoplasma, ELISA)
2. Ensure timely completion of all sample testing, adhering to both Release and Quality timelines.
3. Provide immediate notification of any abnormal test results and assay failures.
4. Prepare all necessary QC sample Material Transfer Document forms for delivery to in-house and third-party laboratories.
5. Support the patient infusion process as required.
6. Prepare documentation in accordance with cGMP guidelines.
7. Assist in writing and revising standard operating procedures (SOPs).
8. Contribute to the writing of deviation and non-compliance investigations.
9. Assist with validation processes and improvements in assays.
Key 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 essential.
- Experience in a clinical laboratory or controlled therapeutic manufacturing environment is highly preferred.
- Ability to work proactively and independently, following through on tasks and projects.
- Action-oriented with a willingness 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 Skills:
- Excellent communication skills, capable of interacting confidently and professionally at all levels.
- Flexibility to adapt to new projects as necessary to support the team.
- Strong planning and prioritization skills 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 excellent benefits offerings
Closing:
MSK is an equal opportunity and affirmative action employer dedicated 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 mandates that employers provide reasonable accommodation 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 accommodation 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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