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Cell Therapy Manufacturing Jobs (NOW HIRING)

AstraZeneca

Lead Cell Therapy Specialist

Tarzana, CA · On-site

In this role, you will lead and coordinate daily manufacturing execution, ensuring personnel ... High School Diploma with at least 5 years of relevant cell therapy, pharmaceutical, biotech, or GMP ...

Bristol Myers Squibb

Manufacturing Associate

Summit, NJ · On-site

$27.83 - $33.72/hr

Execute Cell Therapy Manufacturing operations in compliance with Source Governing Documents (SOPs, Work Instructions, Batch Records, Forms) * Prioritize safety; report safety events within 24 hours ...

Lancesoft

Cell Therapy Specialist

Frederick, MD · On-site

$28 - $30/hr

The Cell Therapy Specialist 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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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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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.
Director, Operational Excellence- Cell Therapy Manufacturing

Director, Operational Excellence- Cell Therapy Manufacturing

AstraZeneca

Rockville, MD • On-site

$148 - $222K/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 2 days ago

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 71 rated pharmaceutical

Job description

About the role, the Director, Operational Excellence (OE) leads the network-wide OE agenda for AstraZeneca's autologous Cell Therapy. You will establish basic conditions and eliminate waste across the vein-to-vein value stream. You will operate in a matrix with site-based OE Leads. It sets strategy, governs the improvement portfolio, and delivers measurable outcomes in cost, productivity, service, quality, safety, and compliance. Additionally, it builds sustainable capabilities for scale.
This role offers flexibility to be based in Rockville, MD or Tarzana, CA.
You Will:
  • Lead end-to-end value stream mapping. Deploy Hoshin/strategy deployment to translate targets, such as COGM, capacity, and service, into a governed portfolio. This portfolio have clear owners, milestones, risks, and benefits. Additionally, create standardized COGM/productivity dashboards and benefit tracking with Finance.
  • Lead programs (cycle time, labor models, MES/EBR enablement, yield, changeovers/scheduling, deviation reduction, automation/technology insertion). Apply the AZ Lean Model (A3, VSM, standard work, daily/tier management, leader standard work, adapted SMED).
  • Facilitate development of business processes for training, batch execution, deviations, and patient/lot scheduling and logistics.
  • Lead Kaizen events; scale best practices across the Cell Therapy Development and Operations.
  • Define basic conditions for Cell Therapy Manufacturing Sites and build capability at all levels; coach leaders and value stream owners
  • Partner with Supply Chain to vein-to-vein flow, slotting, and cold-chain logistics, safeguarding Chain of Identity/Chain of Custody.
  • Ensure improvements uphold safety, patient focus, and cGMP for ATMPs (including GAMP and data integrity). Partner with Quality to reduce human error and increase First Pass Success and right-first-time performance.
  • Align senior leaders on priorities and resources; communicate impact through governance forums.

You Have :
  • Bachelor's in engineering/Life Sciences or related; advanced degree preferred.
  • 10+ years in GMP manufacturing; 5+ years leading programs.
  • Recognized Lean Six Sigma Black Belt or equivalent depth of OE expertise.
  • COGM/productivity improvements using lean, digital, and analytics.
  • Expertise in value stream management and lean (Hoshin, A3, VSM, standard work, tier/visual management, leader standard work); Genba execution.
  • Command of cGMP, data integrity, and GAMP; experience with MES/EBR/LIMS and other digital systems
  • Track record in cross-site program leadership, portfolio governance, and benefits realization with Finance.
  • Demonstrated experience in Influence without authority, change leadership, and process/project/risk/Analytical skills.

The annual base pay for this position ranges from $148 to $222K. Our positions offer eligibility for multiple incentives an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
12-Jun-2026
Closing Date
09-Jul-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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