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Cell Therapy Process Development Jobs in Virginia

Inova Health System

Oncology Hospitalist (MD/DO)

Fairfax, VA · On-site

$128.75 - $170/hr

Partner with the cell therapy physician to round jointly and make medical decisions using a co ... Ability to successfully complete the credentialing process by third-party payors and Ability to ...

Inova

Oncology Hospitalist (MD/DO)

Fairfax, VA · On-site

$127.75 - $168.75/hr

Partner with the cell therapy physician to round jointly and make medical decisions using a co ... Ability to successfully complete the credentialing process by third-party payors and Ability to ...

Inova

Oncology Hospitalist (MD/DO)

Fairfax, VA · On-site

$128.75 - $170/hr

Partner with the cell therapy physician to round jointly and make medical decisions using a co ... Ability to successfully complete the credentialing process by third-party payors and Ability to ...

Inova Primary Care

Oncology Hospitalist (MD/DO)

Fairfax, VA

$127.75 - $168.75/hr

Partner with the cell therapy physician to round jointly and make medical decisions using a co ... Ability to successfully complete the credentialing process by third-party payors and Ability to ...

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Cell Therapy Process Development information

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.
What are popular job titles related to Cell Therapy Process Development jobs in Virginia? For Cell Therapy Process Development jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Cell Therapy Process Development jobs in Virginia look for? The top searched job categories for Cell Therapy Process Development jobs in Virginia are:
What cities in Virginia are hiring for Cell Therapy Process Development jobs? Cities in Virginia with the most Cell Therapy Process Development job openings:
Cell Therapy Process Development jobs near you
Infographic showing various Cell Therapy Process Development job openings in Virginia as of August 2026, with employment types broken down into 66% Full Time, and 34% Part Time. Highlights an 100% In-person job distribution.

Scientist- Oncology Cell Therapy

Kelly Services

Arlington, VA

$48/hr

Full-time, Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 16 days ago

Job description

Kelly Science is seeking a Scientist- Oncology Cell Therapy for a fully benefited long term contract with a growing company located in Gaithersburg, MD.
 
Pay: $48.00/hour
Shift: Monday-Friday 1st Shift
Employment Type: Full Time; 12-month contract
 
Position Summary:
We are seeking a talented Scientist or Senior Scientist to join our dynamic team focused on developing next-generation CAR-T and T cell-based therapies for solid tumors. In this role, you will design and execute laboratory experiments, develop and optimize methods, and analyze scientific data to advance our immunotherapy programs. You’ll play a key part in preclinical oncology studies, collaborating with cross-functional teams to achieve project milestones in a productive and supportive environment.
 
Essential Skills & Experience:
  • BS with 5+ years, MS with 2+ years of relevant experience
  • Strong hands-on experience in in vivo preclinical models and oncology studies.
  • Strong experience with CAR-T cell therapies.
  • Hands-on in vitro experience supporting T cell research.
  • Excellent verbal and written communication skills.
  • Proven ability to work collaboratively in cross-functional teams.
Preferred Qualifications:
  • Experience with flow cytometry and immune cell profiling.
  • Skilled in cell-based functional assays (cytotoxicity, proliferation, cytokine analysis).
  • Experience with primary human T cell isolation, activation, and functional characterization.
  • Familiarity with viral or non-viral genetic modification of T cells.
  • PBMC manipulation and assay experience.
  • Knowledge of solid tumor models and molecular biology skills.
 
Interested? Please apply today for immediate consideration!
 
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.