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Cell Therapy Process Development Jobs in Gainesville, FL

Kincell Bio, LLC

Supervisor, Manufacturing

Gainesville, FL · On-site

$54K - $74K/yr

Experience in cell gene therapy manufacturing and/or aseptic processing. Management ... Possible Process Development supporting autoclaving, cleaning, & prep work * Media and Buffer Prep ...

Kincell Bio, LLC

Office Coordinator

Gainesville, FL · On-site

$16.25 - $21.75/hr

... process development and GMP manufacturing, testing and release from early clinical to pivotal ... Kincell Bio is focused on supporting innovative companies developing immune cell therapies ...

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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 Gainesville, FL is $30.52, according to ZipRecruiter salary data. Most workers in this role earn between $25.05 and $37.45 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.
What are popular job titles related to Cell Therapy Process Development jobs in Gainesville, FL? For Cell Therapy Process Development jobs in Gainesville, FL, the most frequently searched job titles are:
What job categories do people searching Cell Therapy Process Development jobs in Gainesville, FL look for? The top searched job categories for Cell Therapy Process Development jobs in Gainesville, FL are:
What cities near Gainesville, FL are hiring for Cell Therapy Process Development jobs? Cities near Gainesville, FL 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 Gainesville, FL as of August 2026, with employment types broken down into 69% Full Time, and 31% Part Time. Highlights an 100% In-person job distribution, with an average salary of $63,475 per year, or $30.5 per hour.

Contingent Worker, Manufacturing Associate I

Kincell Bio, LLC

Gainesville, FL • On-site

Full-time

Posted 7 days ago

Job description

Kincell Bio engineers cells into therapies. With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. Kincell Bio is focused on supporting innovative companies developing immune cell therapies, including autologous and allogeneic CAR-T, TCR, TILs, Tregs and CAR-NK technologies. We offer challenging career opportunities, competitive benefits, and an environment that recognizes and rewards performance.
For more information, please visit our website at www.kincellbio.com.
As a Contingent Manufacturing Associate I, you will be operating automatic and manual cell and gene therapy equipment with a variety of complexities in CAR-T, CAR-M, or CAR-NK processes in accordance with standard operating procedures and policies. You will perform quality control analyses as required to complete in-process batches and identify variations. You will be trained in handling hazardous materials and emergency procedures since you will be handling leukapheresis cellular materials.
As part of manufacturing operations, you will be relied on to have a good understanding of procedures, techniques, tools, materials, and equipment. Your work and decision-making will be team-based and will focus on the prioritization of workflows centered on the process and available resources. You will follow standard operating procedures to complete tasks which may vary in scope, complexity, and timing.
Patients need individuals who take pride in their work and look for successful outcomes. You will be operating cell and gene therapy process equipment of varying complexity with different processes in accordance with standard operating procedures.
Essential Duties and Responsibilities
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document.
  • Working knowledge of Word and Excel
  • Demonstrate Aseptic Qualification
  • Maintaining personal responsibility with Personal Protective Equipment (PPE)
  • Be a collaborator when a team develops Standard Operating Procedures or Manufacturing Batch Records
  • Conduct Quality Control analyses in a Manufacturing setting
  • Able to learn how to handle materials and bring them into a Manufacturing cleanroom.
  • Clean Equipment and Manufacturing Suite / Rooms
  • Be accountable for your own Safety. Also, be accountable for maintaining your own training requirements.
  • Collaborate with the Investigation team when investigating Quality and Safety Incidents
  • Author Minor Quality / Safety Incident Investigation (Deviations) and Minor CAPAs
  • Develop a knowledge of GXP procedures (GMP, GLP, GCP, GDP, etc.)
  • Must help with cleaning with Equipment and Manufacturing process rooms.
  • Contribute to the team's success by sharing knowledge.
  • Review of Applicable Logbooks
  • Support and Conduct Enrollment of Materials / Bill of Materials.
  • Create Purchase Requests / Procuring Items as needed.
  • Escort Vendors / Visitors into the cleanroom
  • Conduct post-campaign line or area clearance

Qualifications
The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully.
Required:
  • Bachelor of Science degree in Natural Sciences (i.e., Biology, Chemistry, etc.) or Engineering (Chemical, Biomedical, etc.) and 0-2 years of manufacturing experience required or equivalent combination of education and experience.
  • Must be able to work 40 hours per week.
  • Ability to work independently and stay on task in a fast-paced environment without direct supervision.
  • Must be able to recognize when processes, procedures, equipment, products, materials, etc. are out of specification.
  • Hiring will be contingent on passing a visual acuity test. Proof of passing a visual acuity test within the past year will be accepted
  • Effective oral communication.
  • Ability to work well with others in a collaborative team environment.
  • Regular and reliable performance and attendance are required.
  • Able to work in a rapidly changing climate - reacts well to change.
  • Must be able to perform mathematical calculations such as converting milliliters to liters or grams to kilograms. Understands significant figures and rounding.
  • Must be able to lift bags and/or containers of media.
  • Must be able to stand and/or sit for extended periods.
  • Manage your own time and professional development. Be accountable for your own results and prioritized workflows.

Preferred:
  • Have knowledge of cell and gene therapy processing, the metric system, and scales.
  • cGMP clean room experience.

Physical Requirements
  • Vision Acuity Testing
  • Use of a Face Mask

Travel Requirements
  • None

Location
  • This is a site-based temporary position located in Gainesville, FL, and will require some non-standard working hours, including scheduled early mornings, late evenings, and/or weekends.

#LI-Onsite
Kincell Bio provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. Kincell Bio complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
NOTE TO EMPLOYMENT AGENCIES: Kincell Bio values our relationships with our Recruitment Partners. We will only accept resumes from those partners who have been contracted by a member of our Human Resources team to collaborate with us. We are not responsible for any fees related to resumes that are unsolicited or are received without contract.

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