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Cell Therapy Process Development Jobs (NOW HIRING)

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Cell Therapy Process Development information

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How much do cell therapy process development jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for cell therapy process development in the United States is $33.68, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $41.35 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a cell therapy process development professional?

To thrive in Cell Therapy Process Development, you need a solid background in cell biology, biotechnology, or a related field, often supported by a relevant degree and experience with cell culture techniques. Familiarity with bioprocessing equipment, Good Manufacturing Practice (GMP) regulations, and analytical tools such as flow cytometry and PCR is typically required. Strong problem-solving skills, attention to detail, and effective teamwork enhance performance in this collaborative and innovative environment. These competencies ensure the safe and efficient development of cell therapies, meeting rigorous quality standards and advancing clinical applications.

What are some typical challenges faced by professionals in cell therapy process development, and how are they addressed?

Professionals in Cell Therapy Process Development often encounter challenges such as scaling up production processes from laboratory to clinical or commercial scale while maintaining product quality and consistency. Additional hurdles include adhering to strict regulatory requirements and managing complex collaborations across cross-functional teams, like quality assurance, regulatory affairs, and manufacturing. These challenges are typically addressed through rigorous process optimization, thorough documentation, and ongoing communication with stakeholders to ensure that all aspects of the process meet industry standards and regulatory expectations.

What is the difference between Cell Therapy Process Development vs Cell Therapy Manufacturing Specialist?

AspectCell Therapy Process DevelopmentCell Therapy Manufacturing Specialist
CredentialsTypically requires a degree in biology, biochemistry, or biomedical engineering; certifications in GMP or cell therapy are commonSimilar credentials; often holds degrees in related fields and GMP certifications
Work EnvironmentResearch labs, development facilities, early-stage process optimizationManufacturing plants, production floors, quality control labs
Industry UsageFocuses on developing and optimizing cell therapy processesInvolved in large-scale production and process execution

Cell Therapy Process Development professionals focus on designing and refining cell therapy procedures, while Cell Therapy Manufacturing Specialists handle the production and quality assurance in manufacturing settings. Both roles require similar educational backgrounds and certifications but differ mainly in their work environment and specific responsibilities.

What is cell therapy process development?

Cell Therapy Process Development refers to the design, optimization, and scaling up of manufacturing processes for cell-based therapies, such as CAR-T cells or stem cell products. Professionals in this field work on translating laboratory research into reproducible, efficient, and safe production methods that meet regulatory standards. This involves working with cell culture techniques, bioreactors, quality control, and process validation to ensure that therapies can be produced consistently for clinical and commercial use. The goal is to develop robust processes that deliver safe and effective cell therapies to patients.
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What cities are hiring for Cell Therapy Process Development jobs? Cities with the most Cell Therapy Process Development job openings:
What states have the most Cell Therapy Process Development jobs? States with the most job openings for Cell Therapy Process Development jobs include:
What job categories do people searching Cell Therapy Process Development jobs look for? The top searched job categories for Cell Therapy Process Development jobs are:
Infographic showing various Cell Therapy Process Development job openings in the United States as of August 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% In-person job distribution, with an average salary of $70,060 per year, or $33.7 per hour.

Director of Product Sciences, Cell Therapy Analytical Development

Novartis

East Hanover, NJ • On-site

$19K - $288K/yr

Full-time

Medical, Retirement, PTO

Re-posted 21 days ago


Novartis rating

7.5

Company rating: 7.5 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

64th of 86 rated pharmaceutical


Job description

Job Description Summary

Position: Director of Product Sciences – Cell Therapy Analytical Development
Location: East Hanover, NJ, United States (On-Site)
LI #onsite
Novartis: Pioneering New Frontiers: At Novartis, our mission in Cell Therapy Analytical Development and Operations is to innovate for patient benefit. We are seeking an inspiring Director of Product Sciences to design, lead, and support implementation of analytical CMC strategies to de-risk and enable early-to-late clinical development and commercialization of groundbreaking Cell Therapy products.
Your Impact: As the Director of Product Sciences, you will lead cross functional teams and drive product understanding by extended characterization, your wealth of knowledge in Immunology, Process and Analytics. You will be instrumental in shaping our product characterization landscape, setting standards, and guiding our product portfolio’s analytical strategies from inception to commercialization.


Job Description

Key responsibilities:

  • Generate, incorporate, and commoditize product knowledge linking immunological first-principles, patient starting material characteristics, process performance, product quality, and patient clinical outcomes via correlative analysis and mechanistic studies to support and enable Targe Product Profile.
  • Establish guidance and framework to standardize product characterization strategies. Assess and define attribute criticality (CQA vs non CQA), specification setting, and control strategy justification to enable patient access to safe and efficacious cell therapy products.
  • Advance product pipeline through expended capabilities and innovation to enable continued product and process understanding, extended characterization of cell therapy product, process intermediates and starting materials to inform new cell therapy programs and improve manufacturing success.
  • Serve as subject matter expert in T cell immunology, patient starting material and cell therapy product characteristics. Design extended /exploratory characterization assays to assess T cell lineage, cytokine and effector molecule secretion and intracellular production; proliferation, degranulation, and cytotoxicity; memory composition, differentiation, and exhaustion/anergic/activation status; chemokine/trafficking receptor expression; and polarization states.
  • Collaborate with cross functional teams including Analytical Development, Process Development, Quality Control, Quality Assurance, Regulatory CMC, Biostatistics to drive pipeline cell therapy products forward.
  • Drive data-driven decision-making by ensuring effective data management, analysis, and reporting, and support regulatory filings as required.

Requirements:

  • Ph.D. in Immunology or a related field with 10 years of experience in understanding and characterizing the human immune system and cell products.
  • A minimum of 5 years of industry experience in Cell Therapy CMC development is required.
  • A minimum of 5 years of leadership skills, encompassing both direct and matrix management.
  • Proven track record in early to late phase development, commercialization, and life cycle management of cell therapy products.
  • Technical expertise in cell therapy process and product characterization, and correlative analysis.
  • Extensive experience in regulatory filing requirements and addressing health authority questions.
  • Exceptional communications, scientific writing, and presentation skills.

Desirable Requirements:

  • Hands-on interest and experience in relevant analytical methods.
  • Strong foundation and practical experience in statistics.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining

to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Commitment to Diversity & Inclusion: The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.

Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between $192,00-$288,000/year; however, while salary ranges are effective from 1/1/24 through 12/31/24, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers who are focused on building and advancing a culture of inclusion that values and celebrates individual differences, uniqueness, backgrounds and perspectives. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to fostering a diverse and inclusive workplace that reflects the world around us and connects us to the patients, customers and communities we serve.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$192,000.00 - $288,000.00


Skills Desired

Budget Management, Coaching Skills, Data Science, Experiments Design, Laboratory, Npi (New Product Introduction), People Management, Problem Solving Skills, Process Simulation, R&D, Waterfall Project Management

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