Assistant, Cell Manufacturing
About The Position
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. Cell Manufacturing Assistant, Biotherapeutics Core Facility Exciting Opportunity at MSK: The Biotherapeutics Core Facility (BTCF) develops, validates, and implements procedures critical to gene transfer-related clinical research including: genetic engineering and ex vivo transduction of patient cells, cell line development, vector production, R&D and process development work relating to vector production and transduction of patient cells, analysis of gene transfer efficiency and transgene expression in patient cells. We are seeking a meticulous and proactive individual who has excellent organizational skills and strong attention as a Cell Manufacturing Assistant to assist in the aforementioned areas under general supervision Role Overview: cGMP Manufacturing: Participate in the cGMP Production of large-scale clinical-grade products such as, NK, TCR, and T cell products Tech Transfer activities: Assist in the production/development and quality control of ancillary cells, such as master cell banks Analyze gene expressions in cell lines, primary cell lines, and research samples using FACS, PCR, qPCR, etc Participate in process validation and tech transfer activities Participate in planning and discussion of laboratory projects with team leaders and managers Operates and maintain complex laboratory equipment such as FACS machine, qPCR machine, cell washers, and bioreactors Complete all documentation per GDP and cGMP regulation per BTCF’s SOPs and maintaining detailed experimental records Proactively participate in data analysis, data summary, data evaluation, and maintenance of corresponding databases in an accurate and timely fashion Development, writing and updating of SOPs and material lists General lab upkeep and organization
Requirements
- BA/BS with five (5) years related experience or MA/MS with three (3) years related experience; previous experience in cGMP or clinically regulated environment and knowledge of biotechnologies are strongly preferred.
- Must have experience with molecular and/or cellular biology techniques.
- Knowledge of basic computer applications and ability to use MS Office software
- Excellent communication skills and the ability to interact across all levels in a confident, professional manner.
- Ability to independently resolve issues and questions.
- Flexible to adapt to new projects as required for the support of the group.
- Capable of successfully prioritizing tasks.
- A good decision-maker, with proven success at taking initiative and making timely decisions that keep the organization moving forward.
- Ability to work in a fast-paced environment with a positive attitude
- Ability to carry out assignments in a thorough, conscientious fashion.
- Ability to follow detailed instructions, maintain accurate records and notes.
- Ability to work well in a team environment.
Responsibilities
- Participate in the cGMP Production of large-scale clinical-grade products such as, NK, TCR, and T cell products
- Assist in the production/development and quality control of ancillary cells, such as master cell banks
- Analyze gene expressions in cell lines, primary cell lines, and research samples using FACS, PCR, qPCR, etc
- Participate in process validation and tech transfer activities
- Participate in planning and discussion of laboratory projects with team leaders and managers
- Operates and maintain complex laboratory equipment such as FACS machine, qPCR machine, cell washers, and bioreactors
- Complete all documentation per GDP and cGMP regulation per BTCF’s SOPs and maintaining detailed experimental records
- Proactively participate in data analysis, data summary, data evaluation, and maintenance of corresponding databases in an accurate and timely fashion
- Development, writing and updating of SOPs and material lists
- General lab upkeep and organization
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
1,001-5,000 employees
