1

Car T Cell Therapy Manufacturing Associate Jobs

$110K - $145K/yr

Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of ...

We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies ... Perform and verify manufacturing activities for commercial and clinical cell therapy products in ...

New

We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies ... Perform and verify manufacturing activities for commercial and clinical cell therapy products in ...

We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies ... Perform and verify manufacturing activities for commercial and clinical cell therapy products in ...

Showing results 21-40

Car T Cell Therapy Manufacturing Associate information

See salary details

$12

$20

$33

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.

Manager, CAR-T Cell Collection Operations

Remote

Full-time

Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Johnson & Johnson rating

8.3

Company rating: 8.3 out of 10

Based on 113 frontline employees who took The Breakroom Quiz


Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Procurement

Job Sub Function:

Strategic Sourcing

Job Category:

Professional

All Job Posting Locations:

Raritan, New Jersey, United States of America, Remote (US)

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for a Manager, CAR-T Cell Collection Operations to join our team in Raritan, NJ.

An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.

Remote work options may be considered on a case-by-case basis and if approved by the Company.

Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy. This innovative strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR-T platform and investigational treatment.

Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our cell therapy products? Apply today for this exciting opportunity to be part of the #CAR-T team!

Supported by their direct Senior Manager, the CAR-T Cell Collection Operations Manager coordinates and maintains virtual supplier network of apheresis and cryopreservation starting material for clinical and commercial CAR-T products primarily based in United States. With subject matter expertise, they lead the technical relationship with Operating Company-level cell therapy teams and closely collaborate with commercial CAR-T teams. They will facilitate cell collection site certification activities related to apheresis and cell lab, support/provide training for technicians/nurses as needed, and facilitate near-real-time apheresis and/or cryopreservation quality investigation when required.

The Manager is responsible for effectively collaborating with "hospitals as suppliers" and completes appropriate technical analyses to ensure quality services. They will maintain positive collaborations with other operation groups, identifying options to improve performance. The Manager may implement programs to reduce supply base and achieve cost reduction goals. They will lead supplier capabilities, including capacity planning and inventory management. This role provides global and multi-site support.

Key Responsibilities:

  • Manage and maintain commercial CAR-T apheresis and cryopreservation activities in support of 2500-3000 CAR-T patient commercial supply chain activities.

  • Serve as primary POC for apheresis center, local cryopreservation cell laboratories, as well as, contracted third party apheresis/cryopreservation centers within assigned regions.

  • Serve as apheresis Subject Matter Authority for internal and external teams.

  • Facilitate and conduct site qualification and training for collections and/or cryopreservation requirements.

  • Activate site as approved supplier, prior to First Patient In (FPI) date.

  • Ensure timely receipt of recall communications from apheresis centers and evaluate impact to product quality.

  • Ensure timely release of quality fresh/cryopreserved apheresis starting material.

  • Complete quality issues management within 24-48 hours post apheresis.

  • Complete risk and change management.

  • Develop solid understanding of information technology, logistic transport and regulatory requirements affecting collection and cryopreservation of apheresis starting material.

  • Maintain metrics to manage site performance.

Qualifications:

Education:

  • Minimum of a Bachelor's/University or equivalent degree required; focused degree in Nursing, Medical Laboratory Science, or equivalent scientific or engineering field is preferred

Experience and Skills:

Required:

  • Minimum 6 years of relevant work experience

  • Hands-on experience with Immunology, Cell Biology, Cell Therapy, Apheresis, and/or Cryopreservation

  • Strong communication and interpersonal skills, with the ability to work independently and in a cross-functional team environment, to effectively support supplier relationship with cell collection sites

  • Ability to engage with hospital personnel to communicate specific and technical requirements for apheresis and cell cryopreservation

  • Proven experience with Good Tissue Practices (GTP) and current Good Manufacturing Practices (cGMP)

  • Flexibility to adapt to changing situations and ambiguity, to prioritize tasks according to objectives, and provide problem resolution

  • Strong written and verbal communication skills

Preferred:

  • Hospital experience or understanding of drug development and regulatory submission requirements

  • Experience with quality issues management (e.g., investigations, deviations, CAPAs, etc.)

Other:

  • Requires up to 15% domestic and international travel

  • Requires ability and flexibility to work on weekends/off hours for patient support, including the ability to accommodate different global time zones (i.e., LATAM, NA, and EMEA)

#LI-Remote

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.

If you are under 18 years of age, you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parent's consent for the background check.

Required Skills:

Preferred Skills:

Business Data Analysis, Business Savvy, Category Management Strategy, Consulting, Cost Management, Due Diligence, Market Savvy, Negotiation, Problem Solving, Process Improvements, RFx Management, Risk Assessments, Risk Management, Spend Analysis, Strategic Sourcing, Supplier Collaboration, Technical Credibility, Vendor Management, Vendor Selection

The anticipated base pay range for this position is :

$102,000.00 - $177,100.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation -120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year
Holiday pay, including Floating Holidays -13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave - 80 hours in a 52-week rolling period10 days
Volunteer Leave - 32 hours per calendar year
Military Spouse Time-Off - 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

What Johnson & Johnson employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom