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Cell Therapy Operations Jobs (NOW HIRING)

Supply Chain Technical Lead for Robotics - External Supply and Technical Operations Support Reporting to the Global Head for Cell Therapy Procurement, theSupply Chain Technical Lead for Roboticswill ...

... operations as well as works as part of a team to execute GMP runs in close collaboration with Materials Management, Quality Control and Quality Assurance. Responsibilities of the Cell Therapy ...

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Cell Therapy Operations information

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$11

$26

$53

How much do cell therapy operations jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for cell therapy operations in the United States is $26.24, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $30.29 per hour, depending on experience, location, and employer.

What are some of the unique challenges faced by professionals in Cell Therapy Operations, and how can they be effectively managed?

Professionals in Cell Therapy Operations often encounter challenges related to stringent regulatory requirements, maintaining product quality, and coordinating multidisciplinary teams. Managing these challenges involves rigorous adherence to Good Manufacturing Practices (GMP), continuous training, and clear communication among scientists, quality assurance specialists, and manufacturing staff. Strong project management skills and adaptability are also essential, as processes and technologies in cell therapy are rapidly evolving. Team members benefit from cross-functional collaboration and a proactive approach to problem-solving to ensure safe and timely delivery of therapies to patients.

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

To thrive in Cell Therapy Operations, you need a background in biology or related life sciences, experience with Good Manufacturing Practice (GMP), and familiarity with cell culture techniques. Proficiency with laboratory information management systems (LIMS), aseptic processing, and regulatory documentation is often required, along with certifications such as cGMP or GxP training. Attention to detail, teamwork, and strong problem-solving abilities are vital soft skills for ensuring quality and compliance. These skills and qualities are essential for maintaining product integrity, meeting regulatory standards, and supporting the development of life-saving cell therapies.

What is the difference between Cell Therapy Operations vs Cell Manufacturing Specialist?

AspectCell Therapy OperationsCell Manufacturing Specialist
Required CredentialsBiotech or life sciences degree, GMP trainingBiotech or related degree, GMP certification
Work EnvironmentLaboratories, cleanrooms, production facilitiesManufacturing floors, labs, quality control areas
Industry UsageDeveloping and managing cell therapy processesProducing cells at scale for therapies
Common Search IntentUnderstanding roles in cell therapy operationsJobs related to cell manufacturing processes

Cell Therapy Operations professionals focus on managing and optimizing the entire cell therapy process, including process development and quality assurance. In contrast, Cell Manufacturing Specialists are primarily involved in the production and scaling of cell products. Both roles require similar credentials and work in related environments, but their core responsibilities differ in scope and focus within the cell therapy industry.

What are Cell Therapy Operations?

Cell Therapy Operations refer to the processes and activities involved in the manufacturing, quality control, supply chain, and delivery of cell-based therapies to patients. This field ensures that living cells used for treatments, such as CAR-T therapies, are produced, tested, and distributed under strict regulatory standards. Professionals in Cell Therapy Operations coordinate between research, production, clinical teams, and regulatory bodies to ensure safe, effective, and timely delivery of these advanced therapies. Their work is essential for scaling up cell therapies from research to widespread clinical use.
More about Cell Therapy Operations jobs
Infographic showing various Cell Therapy Operations job openings in the United States as of June 2026, with employment types broken down into 2% Internship, 4% As Needed, 50% Full Time, 40% Part Time, and 4% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $54,588 per year, or $26.2 per hour.
Cell Therapy Manufacturing Specialist

Cell Therapy Manufacturing Specialist

Cellares

Bridgewater, NJ โ€ข On-site

$20 - $45/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 10 days ago


Job description

Position Summary
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Night Shift: 6 PM- 6 AM
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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.ย 
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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. 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