QC Lab Assistant, GMP, Shared Resource Core Facility (Good Manufacturing Practices)
- Pay
- $73,382 – $107,601 per year
- Location
- New York, NY · On-site
- Job type
- Full-time
- Level
- Mid-level
- Experience
- 3+ years
- Education
- Bachelor's degree
- Listed
- 18 days ago
Skills & highlights for this role
- Molecular biology techniques (qPCR, PCR, flow cytometry, DNA extraction)
- Cell-based assays
- CRISPR-mediated gene knockout
- Single cell cloning
- SOP drafting
- Experimental design and planning
- Data analysis, interpretation, and trending
- Laboratory equipment maintenance
- GLP documentation
- Microsoft Word
- Microsoft PowerPoint
- Microsoft Excel
- FlowJo
- GraphPad Prism
Also useful
- GMP compliance
- Cell and gene therapy QC testing
- Assay qualification and method optimization
- Quality systems and data management
About Us
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.
Memorial Sloan Kettering Cancer Center seeks QC Lab Assistant, GMP, Shared Resource Core Facility (Good Manufacturing Practices) in New York, NY to build, compile, review and trend test results details to support the release of cell and gene therapy products manufactured within the GMP Shared Resource Core Facility.
Partner closely with the Manufacturing, Process Development and Quality Assurance teams to support the receipt, handling, processing and testing of Quality Control samples throughout the manufacturing lifecycle. Plan and coordinate QC lab activities and maintain accurate QC documentation, test records and result logs for each manufactured product in compliance with GM requirements and established quality control program.
Support cell therapy operations and contribute to patient infusion activities, quality systems and data management activities. Perform and support analytical development assay activities including assay qualification and method optimization to support product characterization and release testing activities. EEO/VETS/ADA.
REQUIREMENTS: Bachelor's degree or equivalent in Biology, Chemistry, Pharmaceutical Sciences, Biochemistry, or other related scientific field and 3 years of experience in the position offered or related.
Requires 3 years of experience with all of the following: molecular biology techniques like qPCR, PCR, flow cytometry and DNA extraction and cell based assays; gene editing techniques CRISPR mediated gene knock out and single cell cloning; drafting SOPs, designing & planning experiments; data analysis, interpretation and trending; maintaining laboratory equipment and documenting results under GLP conditions; and software application skills including Microsoft Word, PowerPoint, Excel, FlowJo, GraphPad Prism and SnapGene. #LI-DNI Pay Range: $35.59 - $55.18 FSLA Status: Non-Exempt Closing: At MSK, we believe in fair, competitive pay that reflects your job, experience, and skills.
Equal opportunity and legal notices
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.
From Msk's careers page, first listed on Rolev.ai on October 23, 2026. Rolev.ai is not the employer.
How Rolev.ai helps with this application
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Common questions
What is the salary for the QC Lab Assistant, GMP, Shared Resource Core Facility (Good Manufacturing Practices) role at Msk?
The QC Lab Assistant, GMP, Shared Resource Core Facility (Good Manufacturing Practices) posting at Msk states compensation of $73,382 – $107,601 per year. It is listed as a full-time position. Final pay may depend on location, experience, and interview evaluation on Msk's official career site.
Where is the QC Lab Assistant, GMP, Shared Resource Core Facility (Good Manufacturing Practices) job at Msk located?
This QC Lab Assistant, GMP, Shared Resource Core Facility (Good Manufacturing Practices) position at Msk is located in New York, NY (On-site). Always check Msk's application page for specific state eligibility or relocation policies.
What qualifications are required for QC Lab Assistant, GMP, Shared Resource Core Facility (Good Manufacturing Practices) at Msk?
For the QC Lab Assistant, GMP, Shared Resource Core Facility (Good Manufacturing Practices) role, Msk highlights 3+ years of relevant experience; a bachelor's degree; experience with Molecular biology techniques (qPCR, PCR, flow cytometry, DNA extraction), Cell-based assays, CRISPR-mediated gene knockout, Single cell cloning, SOP drafting, Experimental design and planning. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.
How do I apply for the QC Lab Assistant, GMP, Shared Resource Core Facility (Good Manufacturing Practices) position at Msk?
This listing links directly to Msk's Workday application page. You can apply directly on Msk's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.