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Car T Cell Therapy Manufacturing Associate Jobs

$83K - $104K/yr

Legend Biotech is seeking an Associate Scientist, Global MSAT Automation as part of the Global ... cell manufacturing development (CAR-T, stem cell, or autologous/allogeneic therapies strongly ...

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Car T Cell Therapy Manufacturing Associate information

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How much do car t cell therapy manufacturing associate jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for car t cell therapy manufacturing associate in the United States is $20.84, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.32 per hour, depending on experience, location, and employer.

What is a Car T Cell Therapy Manufacturing Associate?

Car T Cell Therapy Manufacturing Associates are specialized professionals responsible for producing chimeric antigen receptor (CAR) T cells, which are used in advanced cancer immunotherapy treatments. They work in highly regulated laboratory or cleanroom environments to isolate, genetically modify, and expand patient-derived T cells according to strict quality and safety standards. Their role involves operating sophisticated equipment, following detailed protocols, and ensuring the final cell therapy product meets all regulatory and clinical requirements before being administered to patients.

What are the key skills and qualifications needed to thrive as a Car T Cell Therapy Manufacturing Associate?

A Car T Cell Therapy Manufacturing Associate needs a strong background in biotechnology, cell culture, and aseptic techniques, often supported by a bachelor’s degree in life sciences or a related field. Familiarity with Good Manufacturing Practices (GMP), laboratory information management systems (LIMS), and cell processing equipment is typically required. Attention to detail, problem-solving, and teamwork are vital soft skills for ensuring precise manufacturing and effective collaboration. These competencies are crucial to maintain product quality, regulatory compliance, and patient safety in the production of advanced cell therapies.

What are some common challenges faced by Car T Cell Therapy Manufacturing Associates during the production process?

Car T Cell Therapy Manufacturing Associates often encounter challenges related to maintaining strict aseptic techniques and adhering to precise protocols, as the process involves handling patient-specific cells in a controlled environment. Ensuring product quality and consistency while working under tight timelines can be demanding, especially given the time-sensitive nature of cell therapies. Additionally, associates must stay updated with evolving regulatory requirements and collaborate closely with quality control and process development teams to troubleshoot and optimize procedures.

What is the difference between Car T Cell Therapy Manufacturing Associate vs Cell Processing Technician?

AspectCar T Cell Therapy Manufacturing AssociateCell Processing Technician
CredentialsTypically requires a Bachelor's degree in life sciences or related fieldOften requires a diploma or associate degree in a relevant science or technical field
Work EnvironmentManufacturing facilities focused on cell therapy production, adhering to GMP standardsLaboratories or manufacturing units involved in cell processing and preparation
Industry UsageCommonly employed in biotech and pharmaceutical companies specializing in cell therapiesUsed across biotech, research labs, and manufacturing plants in cell-based products

The Car T Cell Therapy Manufacturing Associate and Cell Processing Technician roles share similarities in working within cell therapy production environments and requiring knowledge of GMP standards. However, the associate position often demands a higher educational background and involves more responsibilities in manufacturing processes, while the technician role may focus more on hands-on cell processing tasks. Both roles are vital in the development and production of cell therapies, with overlapping skills but different levels of responsibility.

What cities are hiring for Car T Cell Therapy Manufacturing Associate jobs?

Cities with the most Car T Cell Therapy Manufacturing Associate job openings:

What are popular job titles related to Car T Cell Therapy Manufacturing Associate jobs?

For Car T Cell Therapy Manufacturing Associate jobs, the most frequently searched job titles are:

Infographic showing various Car T Cell Therapy Manufacturing Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $43,341 per year, or $20.8 per hour.

Senior Scientist, Allogeneic T-Cell Therapy Process Development

Gaithersburg, MD • On-site

AstraZeneca
Pharmaceutical Product Wholesalers • 10K+ employees

$98K - $135K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz


Job description

Senior Scientist, Allogeneic T-Cell Therapy Process Development: Cell Therapy CMC
Do you have a passion for science? Would you like to apply your expertise to impact a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you!
We are looking for a Senior Scientist to join our Allogeneic T-Cell Therapy Process Development team. In this role, you'll be instrumental in supporting the development of clinical manufacturing processes for allogeneic CAR-T and TCR-T products.
At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person. This is an opportunity to work with curious minds in an inclusive culture, where you'll be evaluating cell therapy process and technology improvements, contributing to process understanding and characterization, and assisting tech transfer to a cGMP environment.
About AstraZeneca in Gaithersburg, MD:
Our Gaithersburg, Maryland facility creates life-changing medicines for people around the world. This campus employs more than 3,500 experts in our field and is only a short drive from Washington, DC. This modern and vibrant scientific campus is the home of R&D and Oncology in the US. Here, we play host to some of the most cutting-edge technology and lab spaces, all designed to inspire collaboration and cross-functional science. We believe employees benefit from being challenged and inspired at work. We are dedicated to creating a culture of inclusion and collaboration.
The Gaithersburg site offers a variety of amenities to help boost productivity and help keep our employees happy and healthy. This includes a fitness center, employee healthcare clinic, electric vehicle charging stations, dry cleaning, full-service cafeteria and copy center. This is where you'll find newly designed, activity-based workspaces to suit a variety of working styles while increasing collaboration between teams.
Summary of the group:
The Allogeneic T-Cell Therapy Process Development team within the Cell Therapy Technical Operations (CTTO) group and Cell Therapy Enterprise Unit is responsible for developing, optimizing, characterizing, and scaling manufacturing processes for allogeneic CAR-T and TCR-T cell therapies. The team supports cell engineering and process development activities required to generate high-quality allogeneic T-cell products, including optimization of gene editing, culture expansion, scale-up, and process characterization strategies. In addition, the group produces material to support IND-enabling studies and works closely with cross-functional partners to enable technical transfer to clinical and commercial manufacturing sites. The team also contributes to product characterization, manufacturing deviation support, regulatory submissions, and continuous improvement of cell therapy manufacturing processes.
Main Duties & Responsibilities:
This position within the Allogeneic T-Cell Therapy Process Development team will involve a substantial amount of hands-on cell culture work, including human CAR-T and TCR-T cell generation, in vitro expansion, scale-up, and characterization of culture processes. The role will require performing gene editing activities and manipulation of human primary cells, while applying strong scientific judgment to support process optimization, process characterization, and development of scalable manufacturing approaches.
As a Senior Scientist, you will independently own the design, execution, analysis, interpretation, and documentation of process development studies. You will be expected to lead studies with minimal supervision, use data-driven decision-making to guide next steps, troubleshoot technical challenges, and contribute to the overall technical strategy for allogeneic CAR-T and TCR-T process development.
This role will also require close cross-functional collaboration with Process Development, Analytical Development, Manufacturing, Quality, Regulatory, and other partner functions to support process understanding, technology transfer, and clinical manufacturing readiness. In addition, you will provide scientific guidance and mentorship to junior scientists and associates, helping to strengthen technical capability, experimental rigor, and effective execution across the team. Responsibilities will include supporting tech transfer activities such as batch record and SOP development, real-time troubleshooting, investigation and impact assessment of deviations, change control management, process monitoring and data analysis, and risk assessments. Additionally, you will author and contribute to development reports, scientific publications, patents, and regulatory filings in different countries and regions. Position may require traveling domestically and abroad.
Required Skills
  • Experience culturing human primary cells (T cell culture experience necessary).

  • Knowledgeable about upstream and downstream process development for cell therapies both laboratory based and tech transfer based

  • Strong flow cytometry T cell characterization experience.

  • Experience engineering cells in scale-up processes with manufacture-ready genome editing tools and DNA/RNA transfection approaches.

  • Familiar with the fundamentals of DOE.

  • Strong background in experimental design and data analysis skills are essential.

  • Ability to think critically, analytically and have demonstrated troubleshooting and problem-solving skills based on deductive reasoning.

  • Excellent teamwork and communication skills including proven technical writing skills are required. Position may require weekend work.

Desired Skills:
  • Knowledge about immunology is highly desirable.

  • Experience with cell editing technologies: CRISPR/Cas9, base editing, etc.

  • Experience with viral transduction techniques desirable.

  • GMP experience preferred.

  • Experience with cell characterization (dPCR, ELISA, NGS) ideal.

  • Scientific rigor in assessing own data and that of others. Utilizes forward-looking perspective to contribute to "go/no go" decisions.

Education/Experience:
  • BS degree in Biochemical Engineering, Biomedical Engineering, Biotechnology, or related field with >6 years of relevant experience or MS degree with a minimum of 4 years or PhD with a minimum of 1 year of relevant proven experience.

Why AstraZeneca?
At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we're opening new ways to work, pioneering cutting edge methods, and bringing unexpected teams together. Interested? Come and join our journey.
So, what's next!
Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it's yours.
The annual base pay for this position ranges from $112,304.00 - $168,456.00. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
03-Sep-2026
Closing Date
29-Sep-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB