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Stem Cell Manufacturing Tech Jobs (NOW HIRING)

RN - Stem Cell Transplant I | The Future of Oncology is in Atlanta! Are you a clinical trailblazer ... Pursue professional growth, keep current with new technology, and maintain all required ...

... the Cell Manufacturing Program (CMP) within the Interdisciplinary Stem Cell Institute ... technology transfers and manufacturing readiness activities, including review of sponsor ...

... the Cell Manufacturing Program (CMP) within the Interdisciplinary Stem Cell Institute ... technology transfers and manufacturing readiness activities, including review of sponsor ...

... the Cell Manufacturing Program (CMP) within the Interdisciplinary Stem Cell Institute ... technology transfers and manufacturing readiness activities, including review of sponsor ...

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... Manufacturing & Technology team based in Somerset, NJ.Role OverviewLegend Biotech is seeking a ... stem cell, or autologous/allogeneic therapies strongly preferred).High proficiency in aseptic ...

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Stem Cell Manufacturing Tech information

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How much do stem cell manufacturing tech jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for stem cell manufacturing tech in the United States is $21.44, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $20.91 per hour, depending on experience, location, and employer.

What is a stem cell manufacturing tech?

Stem Cell Manufacturing Technicians are specialized laboratory professionals who produce, process, and quality-check stem cells for research, clinical, or therapeutic use. They work in controlled environments, following strict protocols to ensure the cells are viable, pure, and safe. Their responsibilities may include preparing culture media, monitoring cell growth, operating bioreactors, and documenting all procedures to comply with regulatory standards. These technicians play a crucial role in supporting advances in regenerative medicine and cell therapy.

What are some common challenges faced by stem cell manufacturing techs in maintaining product quality and consistency?

Stem Cell Manufacturing Technicians often encounter challenges in maintaining strict adherence to Good Manufacturing Practice (GMP) protocols, as even small deviations can impact cell quality and safety. Ensuring sterility and preventing contamination in a cleanroom environment is critical and requires strong attention to detail and careful handling of materials. Additionally, technicians must consistently document every step of the process and adapt to evolving standard operating procedures, which may change as new research or technology is implemented. Collaboration with quality control and research teams is essential to troubleshoot issues and uphold the highest standards in product consistency.

What are the key skills and qualifications needed to thrive as a stem cell manufacturing tech, and why are they important?

To thrive as a Stem Cell Manufacturing Tech, you need a background in cell biology or biotechnology, experience with aseptic techniques, and at least a bachelor’s degree in a life science field. Familiarity with Good Manufacturing Practice (GMP) regulations, bioreactor operation, and specialized laboratory equipment is typically required. Attention to detail, strong problem-solving skills, and effective teamwork help ensure process accuracy and regulatory compliance. These skills and qualities are critical for producing high-quality, safe cell therapy products in a tightly regulated environment.

What are popular job titles related to Stem Cell Manufacturing Tech jobs?

For Stem Cell Manufacturing Tech jobs, the most frequently searched job titles are:

Infographic showing various Stem Cell Manufacturing Tech job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 2% As Needed, 88% Full Time, 4% Part Time, 2% Contract, and 3% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $44,602 per year, or $21.4 per hour.

Cellular Biologist II, Global Stem Cell Array

New York, NY

The Jackson Laboratory
Biotechnology Research and Development • 1 - 5K employees

$73K - $82K/yr

Full-time

Posted 26 days ago


The Jackson Laboratory rating

8.6

Company rating: 8.6 out of 10

Based on 24 frontline employees who took The Breakroom Quiz


Job description

EMPLOYER: The Jackson Laboratory

POSITION: Cellular Biologist II, Global Stem Cell Array

DUTIES: The Cellular Biologist II, Global Stem Cell Array, performs project planning, experimental design, method development, execution of laboratory procedures, adaptation of protocols, data collection and analysis, documentation, and contribution to reports and other written materials for human/mammalian cell culture. Primary responsibilities include implementing and performing cell biology related tasks and procedures; planning and monitoring resources needed to conduct tasks such as the cell culture (manual or automated), spatial transcriptomics, and hyperplexed imaging technologies of the laboratory; maintaining inventory control; coordinating space, field, equipment, and/or facilities; may monitor expenditures; documentation of results; implementing protocols from the literature; identifying problems, troubleshooting, and analyzing variations observed and reported in regular testing protocols; modifying, refining, or adapting techniques and procedures; modifying and/or adjusting quality control measures; leading exchange of research information through demonstration and instruction; performing and independently monitoring automated and manual cell culture and related activities; adapting protocols and developing new workflows with periodic support as required; working collaboratively to perform all necessary protocols for workflows that include, but are not limited to, fibroblast expansion, reprogramming, iPSC expansion on the robotic platform(s), or manually as required; storing and withdrawal of specimens from liquid nitrogen and freezers and prepare media and reagents required for daily work; working closely with the laboratory operations team to ensure reagent/consumable inventory is accurately and efficiently stocked; planning and monitoring resources needed to operate the Global Stem Cell Array; maintaining inventory control; coordinating space and field questions; may be required to participate in the monitoring and tracking of resources/expenditures across projects; working closely with departmental leadership and a multidisciplinary team of scientists and technical specialists; and providing documentation and feedback including the creation and modification of SOPs, filing of file tickets to software and automation teams, and providing feedback at inter- and intra-team meetings. The role will be in regular collaboration with cross functional partners such as project managers, engineering teams, and software or technical support personnel to ensure smooth day-to-day laboratory operations in a production focused environment and will collaborate with engineers and other staff when resolving more complex issues.

RATE OF PAY: Between $73,382 and $82,311 per year.

REQUIREMENTS: Bachelor's degree or foreign equivalent in a directly related specialty of biology, such as biotechnology, forensic science, or biology, and two years of experience in a professional laboratory scientific role performing both automated and manual cell culture operations for induced pluripotent stem cell (iPSC) lines in compliance with Laboratory Information Management Systems. Additionally all qualified applicants must have experience with the following proficiencies/ skills over a period of 24 months: (1) Automated iPSC Derivation and Cell Culture Operations including production and handling of biological materials to support automated induced pluripotent stem cell (iPSC) reprogramming, expansion, maintenance and assay execution, including robotic media exchange, passaging, thawing, and cryopreservation; (2) Processing whole blood, skin, saliva, and fibroblast samples; isolation of PBMCs using manual and automated array systems; preparation of biological inputs for downstream reprogramming and discovery workflows within Laboratory Information Management Systems platforms; (3) Executing fibroblast reprogramming protocols, initiation of stem cell discovery pipelines, and transition of primary cell types into pluripotent states under controlled manual and automated conditions; (4) Implementation, development, and continuous improvement of novel automated assays and workflows; analysis and assessment of robotic system performance; identification and resolution of automation related process issues affecting biological sample production; and (5) Maintenance of organized, accurate records; independent troubleshooting with concise error reporting to scientific teams; exclusive use of the Laboratory Information Management Systems tracking system for sample and process traceability.

ADDRESS OF EMPLOYMENT: The Jackson Laboratory, 619 W. 54th Street, New York, NY 10019

About JAX:

The Jackson Laboratory is an independent, nonprofit biomedical research institution with a National Cancer Institute-designated Cancer Center and nearly 3,000 employees in locations across the United States (Maine, Connecticut, California),Japan andChina. Its mission is to discover precise genomic solutions for disease and empower the global biomedical community in the shared quest to improve human health.

Founded in 1929, JAX applies over nine decades of expertise in genetics to increase understanding of human disease, advancing treatments and cures for cancer, neurological and immune disorders, diabetes, aging and heart disease. It models and interprets genomic complexity, integrates basic research with clinical application, educates current and future scientists, and provides critical data, tools and services to the global biomedical community. For more information, please visitwww.jax.org.

EEO Statement:

The Jackson Laboratory provides equal employment opportunities to all employees and applicants for employment in all job classifications without regard to race, color, religion, age, mental disability, physical disability, medical condition, gender, sexual orientation, genetic information, ancestry, marital status, national origin, veteran status, and other classifications protected by applicable state and local non-discrimination laws.


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