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Car T Cell Therapy Analytical Development Jobs (NOW HIRING)

... analyses to ensure quality services. They will maintain positive collaborations with other ... Hands-on experience with Immunology, Cell Biology, Cell Therapy, Apheresis, and/or Cryopreservation

... development, validation and execution of high-throughput cell-based assays to characterize CAR-T ... Therapy, Antibody Engineering, and Protein Chemistry groups to advance T cell therapies. The ...

... the discovery and development of novel engineered CAR T and eTCR T cell therapeutics for the ... Strong quantitative and analytical skills are desirable Compensation Overview Seattle - WA: $152 ...

... for our CAR-T cell therapy products. The successful candidate will work with a talented and ... in analytical method development, qualification, and method transfer activities within the ...

NJ · On-site

... for our CAR-T cell therapy products. The successful candidate will work with a talented and ... in analytical method development, qualification, and method transfer activities within the ...

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Car T Cell Therapy Analytical Development information

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$37.5K

$75K

$111.5K

How much do car t cell therapy analytical development jobs pay per year?

As of Sep 9, 2026, the average yearly pay for car t cell therapy analytical development in the United States is $74,986.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,000.00 and $93,000.00 per year, depending on experience, location, and employer.

What is Car T Cell Therapy Analytical Development?

CAR T Cell Therapy Analytical Development refers to the process of designing, optimizing, and validating laboratory tests used to assess the quality, potency, safety, and consistency of CAR T cell therapies during their research, manufacturing, and clinical development. Professionals in this field develop and implement assays to characterize CAR T cells, monitor their function, and ensure compliance with regulatory standards. Their work is crucial for advancing CAR T cell products from early-stage research through clinical trials and into commercial manufacturing, ultimately ensuring that these innovative therapies are both safe and effective for patients.

What are the key skills and qualifications needed to thrive in Car T Cell Therapy Analytical Development?

To thrive in CAR T Cell Therapy Analytical Development, you need a solid background in cell biology, immunology, and analytical assay development, usually supported by an advanced degree in a life sciences field. Familiarity with flow cytometry, ELISA, qPCR, and regulatory compliance systems such as GMP is typically required. Strong problem-solving abilities, attention to detail, and effective teamwork are standout soft skills in this area. These skills and qualities are crucial for ensuring the safety, efficacy, and regulatory compliance of innovative cell therapy products.

What are some typical challenges faced by professionals in Car T Cell Therapy Analytical Development, and how can they be managed?

Professionals in CAR T Cell Therapy Analytical Development often encounter challenges such as ensuring assay robustness, maintaining sample integrity, and adapting to evolving regulatory requirements. Handling complex biological materials requires strong attention to detail and the ability to troubleshoot unexpected results. Collaboration with cross-functional teams—such as manufacturing, quality control, and clinical development—is essential to address technical hurdles and implement best practices. Staying updated on the latest technologies and regulatory guidance helps in successfully navigating these challenges and advancing therapeutic programs.

What is the difference between Car T Cell Therapy Analytical Development vs Car T Cell Manufacturing Specialist?

AspectCar T Cell Therapy Analytical DevelopmentCar T Cell Manufacturing Specialist
Primary FocusDeveloping and validating analytical methods to assess CAR T cell productsOverseeing the production and manufacturing processes of CAR T cells
Required SkillsAnalytical techniques, assay development, quality controlManufacturing protocols, GMP compliance, process optimization
Work EnvironmentLaboratories, R&D settingsManufacturing facilities, production floors
Industry UsageUsed in research, development, and quality assurance of CAR T productsUsed in large-scale production and process execution

While both roles are essential in CAR T cell therapy, Analytical Development focuses on creating and validating tests to ensure product quality, whereas Manufacturing Specialists handle the actual production process. Understanding these differences helps in choosing the right career path or job focus within the CAR T cell therapy industry.

What are popular job titles related to Car T Cell Therapy Analytical Development jobs?

For Car T Cell Therapy Analytical Development jobs, the most frequently searched job titles are:

Infographic showing various Car T Cell Therapy Analytical Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $74,986 per year, or $36.1 per hour.

Manager, CAR-T Cell Collection Operations

Remote

Full-time

Retirement, PTO

This job post has expired 2 days ago. Applications are no longer accepted.


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