ZipRecruiter

Log In

1

Cell Therapy Operations Jobs (NOW HIRING)

next page

Showing results 1-20

All JobsCell Therapy Operations Jobs

Cell Therapy Operations information

See salary details

$11

$26

$53

How much do cell therapy operations jobs pay per hour?

As of Jul 11, 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
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 July 2026, with employment types broken down into 1% As Needed, 71% Full Time, 27% Part Time, and 1% Contract. 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.
QC Principal Scientist - Microbiology (Cell Therapy)

QC Principal Scientist - Microbiology (Cell Therapy)

Lonza

Portsmouth, NH • On-site

Full-time

Medical, Dental, Vision, Retirement

Re-posted 19 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

24th of 74 rated pharmaceutical

Job description

QC Principal Scientist - Microbiology (Cell Therapy)
Location: Portsmouth, NH, USA. Relocation assistance is available for eligible candidates.
Schedule: Day Shift, Monday - Friday, 8:00 AM - 5:00 PM (Standard 40-hour week)
As a QC Principal Scientist in our Microbiology department, you serve as the Subject Matter Expert (SME) and technical anchor for our Cell Therapy operations. You are responsible for the strategic oversight of microbial control activities, including method transfers, validation projects, and complex trend analysis. This is a high-level individual contributor role that acts as a technical advisor to site leadership and a mentor to junior staff, ensuring our personalized therapies meet global regulatory standards through scientific excellence.
What You'll Get
  • Technical Authority: Serve as a primary SME for Microbiology, influencing site-wide quality strategy and representing the department in cross-functional leadership teams.
  • Complex Problem Ownership: Lead high-visibility investigations and continuous improvement projects that directly impact the efficiency and compliance of the Cell Therapy asset.
  • Audit Leadership: Play a key role in regulatory inspections, acting as a primary technical witness and SME in both front and back-room settings.
  • Full Lonza Benefits: Medical, dental, vision, 401(k), and performance-based incentives. lonza.com/careers/benefits.

What You'll Do
  • Validation & Method Transfer: Lead the authoring and execution of protocols for method transfers, qualifications, and validations. You will identify technical risks and implement mitigation strategies to ensure on-time program completion.
  • Technical SME Oversight: Provide expert guidance to internal operations and contracted suppliers across a broad spectrum of microbiology disciplines. You will be the technical resource for cross-functional teams involving Manufacturing and Quality Assurance.
  • Audit Participation: Actively participate in internal and external audits (FDA, EMA, etc.). You will be responsible for defending technical data, explaining complex microbial processes, and supporting the "back-room" strategy team.
  • Investigation Leadership: Perform and lead high-complexity deviation and investigation activities. You will apply root cause analysis (RCA) to identify systemic issues and implement effective CAPAs.
  • Compliance & Review: Perform high-level review of laboratory records and author/approve QC SOPs, protocols, and specifications to ensure 100% adherence to cGMP and global regulatory guidelines (USP, EP, JP).
  • Data Mining & Trending: Troubleshoot assay and instrumentation issues through advanced data mining and trend analysis to support long-term laboratory operational health.

Who We're Looking For
  • Education: Bachelor's degree in Microbiology, Biochemistry, or a related Science discipline is required. An Advanced Graduate Degree (Master's or PhD) is highly preferred.
  • Experience: 5-10+ years of relevant experience in a professional GMP environment. You should have a proven track record of managing complex QC projects and leading technical investigations.
  • Technical Mastery: * Broad Microbiological Expertise: Extensive knowledge across multiple disciplines, including Sterility Testing, Endotoxin analysis, and Microbial ID/Genomics.
    • Regulatory Fluency: Expert knowledge of cGMP principles and global pharmacopeia (USP, EP, JP).
    • Systems Proficiency: Advanced experience with Quality Systems such as TrackWise and LIMS.
  • Soft Skills: * Analytical Leadership: Ability to mentor junior staff and resolve technical problems with little to no day-to-day instruction.
    • Strategic Communication: Strong ability to organize technical information into logical, coherent reports and present with confidence to site leadership and regulatory auditors.
    • Initiative: A champion for change who drives successful implementation of new initiatives.

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to lead the science behind the cure? Apply now.

What Lonza employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply