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Cell Therapy Operations Jobs (NOW HIRING)

Novartis

$138K - $257K/yr

Summary #LI-Remote The Associate Director Cell Therapy Operations Manager is in the Southeast geography. This is a remote& field-based role that covers thefollowing, butnot limited to:Atlanta, GA ...

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How much do cell therapy operations jobs pay per hour?

As of Sep 2, 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 is 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.

What are the key skills and qualifications needed to thrive in cell therapy operations?

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 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 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 does a cell therapy operations specialist do?

A cell therapy operations specialist manages the manufacturing, processing, and quality control of cell-based therapies in a laboratory or clinical setting. They ensure compliance with regulatory standards, follow standard operating procedures, and often work with specialized equipment and documentation systems to support the production of personalized or off-the-shelf cell therapies.
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What job categories do people searching Cell Therapy Operations jobs look for?

The top searched job categories for Cell Therapy Operations jobs are:

Cell Therapy Operations jobs near you
Infographic showing various Cell Therapy Operations job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $54,588 per year, or $26.2 per hour.

Associate Director, Cell Therapy Operations- Southeast

Novartis

Remote

$138K - $257K/yr

Full-time

Medical, Retirement, PTO

Re-posted 11 days ago

Novartis rating

7.8

Company rating: 7.8 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical

Job description

Job Description Summary

#LI-Remote
The Associate Director Cell Therapy Operations Manager is in the Southeast geography. This is a remote& field-based role that covers thefollowing, butnot limited to:Atlanta, GA, Charlotte, NC and Jacksonville, FL. Associatemustresidewithin territory, or within a reasonable daily commuting distance of 60 miles from territory.
The Associate Director, Cell Therapy Operations Manager (AD, CTOM) is a field-based operational leader responsible for training, onboarding, and qualifying CAR-T treatment centers to support the safe, compliant, and successful delivery of Novartis CAR-T therapies. The AD, CTOM serves as the primary operational partner to assigned treatment centers, supporting ordering, logistics, apheresis collection, site readiness, quality compliance, and operational excellence while collaborating cross-functionally to resolve complex challenges and improve site performance.


Job Description

Major Accountabilities
  • Execute onboarding, training, qualification, and operational readiness activities for CAR-T treatment centers to support successful site activation and patient treatment.
  • Serve as the field-based operational lead for assigned treatment centers, supporting ordering, logistics, apheresis collection, product receipt, and treatment workflows.
  • Deliver high-quality operational support to treatment centers, care teams, and internal stakeholders to ensure consistent execution of CAR-T processes.
  • Resolve complex operational challenges related to ordering, logistics, apheresis collection, product handling, and site readiness.
  • Ensure compliance with operational, regulatory, quality, and procedural requirements, supporting ongoing inspection and audit readiness.
  • Lead site readiness, operational continuity, and refresher training initiatives to maintain consistent performance and adherence to Novartis standards.
  • Partner cross-functionally with Patient Support, Strategic Account Managers, Quality, Manufacturing, Clinical Operations, Medical Affairs, and other stakeholders to align strategy, improve processes, and drive successful patient outcomes.
  • Identify operational risks, implement process improvements, manage escalations, and drive continuous improvement initiatives across assigned treatment centers.
Minimum Requirements

Education: Bachelor's degree in science, healthcare, nursing, business, or a related discipline.

  • Minimum 7 years of healthcare, pharmaceutical, biotechnology, specialty operations, or related industry experience.
  • Experience supporting complex healthcare systems, treatment centers, academic medical centers, or multi-site institutions.
  • Demonstrated experience in cell therapy operations, specialty therapy operations, or other highly regulated healthcare environments.
  • Proven experience training, onboarding, educating, or supporting external healthcare stakeholders.
  • Ability to effectively operate within matrixed, cross-functional organizations and influence stakeholders without direct authority.
  • Strong project management, problem-solving, and operational execution skills with the ability to manage multiple priorities simultaneously.
  • Excellent communication, presentation, and relationship-management skills with internal and external stakeholders.

Candidate must reside within territory, or within a reasonable daily commuting distance of 60 miles from the territory border. Ability to travel 60-80% over a broad geography is required, with the ability to drive and/or fly within the territory. Must have a valid driver's license.

Preferred Qualifications
  • Direct experience supporting CAR-T, cell therapy, apheresis, blood or tissue collection, cryopreservation, transplant, or related specialty operations.
  • Experience working within GxP-regulated pharmaceutical, biotechnology, manufacturing, cell processing, hospital, or specialty healthcare environments.

The pay range for this position at commencement of employment is expected to be between$138,600.00 and $257,400.00/year; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$138,600.00 - $257,400.00


Skills Desired

Adaptive Strategy And Innovation (Inactive), Clinical Research, Cross-Functional Teamwork, Drug Development, Financial Management, Interpersonal Communication Skills (Inactive), Microsoft Project, Pmi (Project Management Institute) (Inactive), Pmp (Project Management Professional) (Inactive), Product Development, Program Management, Project Delivery, Project Implementations, Project Management Life Cycle (PMLC), Project Planning, R&D (Research And Development) (Inactive), Resource Allocation, Risk Management, Senior Management (Inactive), Stakeholder Management, Time Management Skills (Inactive), Waterfall Model

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