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Cell Therapy Manufacturing Jobs (NOW HIRING)

Lancesoft

Cell Therapy Technician

Frederick, MD · On-site

$25 - $27/hr

The Cell Therapy Technician will perform and/or verify all tasks associated with the manufacture of ... commercial product following batch records and standard operating procedures (SOPs) to ensure safe ...

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Cell Therapy Manufacturing information

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$13

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How much do cell therapy manufacturing jobs pay per hour?

As of Jun 22, 2026, the average hourly pay for cell therapy manufacturing in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

How much does a gene therapy scientist make?

A gene therapy scientist's salary typically ranges from $80,000 to $150,000 annually, depending on experience, education, and location. Senior roles or those with specialized skills in cell and gene editing may earn higher salaries, especially in biotech or pharmaceutical companies involved in cell therapy manufacturing.

Is cell therapy profitable?

Cell therapy manufacturing can be profitable due to high demand for regenerative treatments and personalized medicine. However, it requires significant investment in specialized equipment, skilled personnel, and compliance with regulatory standards, which can impact overall profitability for companies and roles in this field.

What are some common challenges faced in Cell Therapy Manufacturing, and how can new team members prepare for them?

Cell Therapy Manufacturing professionals often encounter challenges such as maintaining strict aseptic conditions, managing complex documentation requirements, and ensuring compliance with evolving regulatory standards. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and staying current on industry regulations. Collaboration with quality control, process development, and regulatory teams is essential for troubleshooting and continuous improvement in this rapidly advancing field.

What is cell therapy manufacturing?

Cell therapy manufacturing involves producing living cells used to treat diseases, such as cancer or autoimmune disorders. It requires specialized facilities, adherence to strict quality standards, and knowledge of bioprocessing techniques to ensure the safety and efficacy of the final product.

What are the key skills and qualifications needed to thrive in Cell Therapy Manufacturing, and why are they important?

To excel in Cell Therapy Manufacturing, a strong background in biology or biotechnology, laboratory techniques, and GMP (Good Manufacturing Practice) compliance is essential, often supported by a relevant degree or certification. Familiarity with bioprocessing equipment, aseptic techniques, and electronic batch record systems is typically required. Attention to detail, teamwork, and strong problem-solving skills help individuals adapt to the complex and regulated environment. These competencies ensure the safe, reliable, and high-quality production of cell-based therapies critical for patient treatment.

What is the difference between Cell Therapy Manufacturing vs Cell Culture Technician?

AspectCell Therapy ManufacturingCell Culture Technician
Required CredentialsTypically requires a Bachelor's degree in biology, biotechnology, or related field; certifications in GMP or cell processing are commonUsually requires a high school diploma or associate degree; some roles may need basic lab certifications
Work EnvironmentCleanroom, GMP-compliant manufacturing facilities, regulated environmentLaboratories, research facilities, or production areas, often less regulated
Employer & Industry UsageBiotech, pharmaceutical companies, cell therapy manufacturing plantsResearch labs, biotech companies, academic institutions

Cell Therapy Manufacturing involves working in regulated, GMP-compliant environments to produce cell-based therapies, requiring specialized training and certifications. In contrast, Cell Culture Technicians focus on maintaining cell cultures in research or less regulated settings, with generally fewer certifications needed. Both roles are essential in the biotech industry but differ in scope, environment, and credential requirements.

Who manufactures CAR-T cell therapy?

Cell therapy manufacturing for CAR-T cell therapy is primarily conducted by biotechnology and pharmaceutical companies such as Novartis, Gilead Sciences (Kite Pharma), and Bristol-Myers Squibb. These companies develop, produce, and distribute CAR-T therapies, which require specialized facilities, quality control, and regulatory compliance. Job roles in this field often involve skills in cell culture, bioprocessing, and Good Manufacturing Practice (GMP).
More about Cell Therapy Manufacturing jobs
What cities are hiring for Cell Therapy Manufacturing jobs? Cities with the most Cell Therapy Manufacturing job openings:
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What job categories do people searching Cell Therapy Manufacturing jobs look for? The top searched job categories for Cell Therapy Manufacturing jobs are:
Cell Therapy Manufacturing jobs near you
Infographic showing various Cell Therapy Manufacturing job openings in the United States as of June 2026, with employment types broken down into 83% Full Time, 13% Part Time, and 4% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.
Cell Therapy Manufacturing Specialist

Cell Therapy Manufacturing Specialist

Cellares

Bridgewater, NJ

$20 - $45/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 17 days ago

Job description

Position Summary
 
Night Shift: 6 PM- 6 AM
 
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Specialist to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. 
 
Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.
Responsibilities
  • Perform routine procedures following written instructions (SOPs, batch records, solution documents, protocols, etc.)
  • Execute manufacturing processes in both an R&D and GMP environments, following protocols and/or standard operating procedures (SOPs)
  • Provide user feedback to engineering and process teams, support with requirements gathering and review
  • Support reagent preparation, leukopak processing, and sample testing in an R&D and GMP environment
  • Contribute to analysis and presentation of technical results at departmental meetings
  • Perform routine clean room and laboratory activities including ordering, cleaning, restocking, and equipment qualification/maintenance
  • Operate in a controlled GMP environment and perform gowning as per procedure
  • Complete required training and ensure compliance with established internal and external control procedures
  • Assist in the execution of process, equipment and cleaning validation
  • Responsible for revising and originating production records, standard operating procedures, protocols and reports
  • Initiate and support the closure of Deviation Reports and CAPAs
  • Train and mentor new manufacturing associates on procedures, aseptic techniques, equipment and trouble-shooting skills
  • Review in-process and completed documents for accuracy and to make sure batch records are turned in to area management within specified days of completion
  • Work with Quality Control, Facilities, Materials Management, Quality Assurance and Validation to complete assignments
  • Other duties as assigned
Requirements
  • Bachelor's Degree or diploma in a scientific or related field is required
  • 1+ years of experience within the biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy
  • Must know and follow job safety procedures, attend required health and safety training, proactively promote safety at work, and promptly report actual and potential accidents and injuries
  • Must comply with the safety policies of the company and site
  • Adherence to cGMPs is required at all times during the manufacturing of Cell Therapy products
  • Proficiency in Drug Product-related process equipment
  • Must have experience following protocols, SOPs, and/or GMP documentation
  • Excellent verbal, written, presentation, and interpersonal skills
  • Strong analytical and problem-solving skills
  • Self-motivated and passionate about advancing the field of cell therapy
  • Self-awareness, integrity, authenticity, and a growth mindset
  • Desire to be part of a rapidly evolving organization, with compelling technology, and take products and processes to the next level
$20 - $45 an hour
Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, and Onsite lunches. All displayed pay ranges are approximate, negotiable, and location dependent.
This is Cellares

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company's Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares' Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.

Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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About Cellares

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

11 - 50 Employees

Headquarters location

South San Francisco, CA, US

Year founded

2019

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