Cell Engineering Quality Assurance Technician

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 future generations. Our dedicated teams provide tailored, compassionate, and expert care to patients of all ages.

Guided by groundbreaking research from our Sloan Kettering Institute, our scientists engage in collaborative efforts 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 nurturing the next generation of scientists and clinicians, who will continue our mission both at MSK and globally.

Please review important announcements about vaccination requirements and our upcoming EHR implementation by clicking here .

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Job Responsibilities:
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 groups to ensure the timely reception and processing of QC samples.

Key Duties:

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 all sample testing is completed in a timely manner, adhering to both Release and Quality timelines.

3. Promptly notify relevant parties of any abnormal test results or assay failures.

4. Prepare all necessary QC sample Material Transfer Document forms for delivery to in-house and third-party laboratories.

5. Provide support during the patient infusion process.

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 to assays.

Essential Qualifications:

1-2 years of laboratory experience is required. Proficiency in molecular biology techniques such as QPCR, PCR, DNA extraction, and cell culture is essential.

Experience in a clinical laboratory or a regulated therapeutic manufacturing environment is highly preferred.

The ability to work independently and proactively, with a strong follow-through on tasks and projects.

Action-oriented and enthusiastic about tackling new challenges with urgency and high energy.

Advanced skills in Microsoft Office applications (Word, Excel, PowerPoint, Outlook) are necessary.

Core Competencies:

Excellent communication skills with the ability to engage confidently and professionally at all levels.

Flexibility to adapt to new projects as required to support the team.

Adept at planning and prioritizing tasks to meet commitments with a keen attention to detail.

Additional Information:
Location: 417 E 68th St, NYC

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.

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