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Cell Therapy Jobs in Spring, TX (NOW HIRING)

Core Technician - Cell Therapy Location: This is an on-site position located in Houston, TX. As a Core Technician - Cell Therapy , you will play a critical role in the manufacturing of clinical and ...

Core Technician - Cell Therapy Location: This is an on-site position located in Houston, TX. As a Core Technician - Cell Therapy , you will play a critical role in the manufacturing of clinical and ...

Core Technician - Cell Therapy Location: This is an on-site position located in Houston, TX. As a Core Technician - Cell Therapy , you will play a critical role in the manufacturing of clinical and ...

Core Technician - Cell Therapy Location: This is an on-site position located in Houston, TX. As a Core Technician - Cell Therapy , you will play a critical role in the manufacturing of clinical and ...

Core Technician - Cell Therapy Location: This is an on-site position located in Houston, TX. As a Core Technician - Cell Therapy , you will play a critical role in the manufacturing of clinical and ...

Core Technician - Cell Therapy Location: This is an on-site position located in Houston, TX. As a Core Technician - Cell Therapy , you will play a critical role in the manufacturing of clinical and ...

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Cell Therapy information

See Spring, TX salary details

$9

$15

$21

How much do cell therapy jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for cell therapy in Spring, TX is $15.50, according to ZipRecruiter salary data. Most workers in this role earn between $13.27 and $17.12 per hour, depending on experience, location, and employer.

What is cell therapy?

Cell therapy is a type of medical treatment that involves the transplantation of live, healthy cells into a patient to repair or replace damaged tissues or cells. This therapy is often used to treat diseases such as certain cancers, blood disorders, and autoimmune conditions. The cells used can come from the patient (autologous) or from a donor (allogeneic). Cell therapy is a rapidly evolving field and is at the forefront of regenerative medicine, offering new hope for conditions that were previously difficult to treat.

What are some common challenges faced by professionals working in cell therapy, and how can they be addressed?

Professionals in Cell Therapy often encounter challenges such as maintaining strict regulatory compliance, ensuring product consistency, and addressing the complexity of manufacturing processes. These challenges can be addressed by staying up-to-date with evolving regulations, implementing rigorous quality control protocols, and working closely with cross-functional teams including quality assurance and regulatory affairs. Additionally, continuous training and adopting new technologies can help streamline workflows and enhance product safety and efficacy.

What are the key skills and qualifications needed to thrive in cell therapy, and why are they important?

To thrive in Cell Therapy, professionals need a solid background in cellular biology, laboratory techniques, and a relevant degree in life sciences or biotechnology. Familiarity with cell culture systems, flow cytometry, Good Manufacturing Practice (GMP) standards, and often certifications like ASCP or relevant laboratory accreditation are essential. Attention to detail, problem-solving, teamwork, and strong communication skills distinguish outstanding candidates in this field. These competencies ensure the safe, precise development and delivery of cell-based treatments, which is critical for patient outcomes and regulatory compliance.

What is the difference between Cell Therapy vs Clinical Research Coordinator?

AspectCell TherapyClinical Research Coordinator
Required CredentialsAdvanced degrees in biology, immunology, or related fields; specialized training in cell processingBachelor's degree in health sciences, nursing, or related fields; certification often preferred
Work EnvironmentLaboratories, manufacturing facilities, hospitals, research centersClinical trial sites, hospitals, research institutions
Employer & Industry UsageBiotech companies, pharmaceutical firms, hospitals involved in cell-based therapiesAcademic institutions, hospitals, clinical research organizations

Cell Therapy professionals focus on developing, manufacturing, and applying cell-based treatments, requiring specialized scientific skills. Clinical Research Coordinators manage clinical trials, ensuring protocol adherence and patient safety. While both roles operate within healthcare and research settings, Cell Therapy roles are more technical and lab-oriented, whereas Clinical Research Coordinators handle trial logistics and compliance.

What are popular job titles related to Cell Therapy jobs in Spring, TX?

For Cell Therapy jobs in Spring, TX, the most frequently searched job titles are:

What job categories do people searching Cell Therapy jobs in Spring, TX look for?

The top searched job categories for Cell Therapy jobs in Spring, TX are:

What cities near Spring, TX are hiring for Cell Therapy jobs?

Cities near Spring, TX with the most Cell Therapy job openings:

Infographic showing various Cell Therapy job openings in Spring, TX as of August 2026, with employment types broken down into 2% As Needed, 71% Full Time, 14% Part Time, and 13% Contract. Highlights an 76% Physical, 1% Hybrid, and 23% Remote job distribution, with an average salary of $32,231 per year, or $15.5 per hour.

Core Technician- Cell Therapy

Lonza

Houston, TX • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 days ago


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

26th of 86 rated pharmaceutical


Job description

Core Technician - Cell Therapy
Location: This is an on-site position located in Houston, TX.
As a Core Technician - Cell Therapy, you will play a critical role in the manufacturing of clinical and commercial cell therapy products within a highly regulated GMP environment. This position is responsible for performing aseptic cell processing activities, operating production equipment, completing GMP documentation, and supporting the safe and compliant manufacture of life-saving therapies. Working closely with Manufacturing, Quality, and Operational teams, you will help ensure products are produced according to established procedures, quality standards, and production schedules.
What you will get:
This is a competitive, hourly paid position. In addition, below you will find a comprehensive summary of the benefits package we offer:
  • Performance-related bonus.
  • Medical, dental and vision insurance.
  • 401(k) matching plan.
  • Life insurance, as well as short-term and long-term disability insurance.
  • Employee assistance programs.
  • Paid time off (PTO).

Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.
What you will do:
  • Participate in the aseptic processing and manufacture of clinical and commercial cell therapy products.
  • Perform aseptic cell culture manipulations within Grade A/B cleanroom environments.
  • Operate cell processing and manufacturing equipment according to approved SOPs.
  • Troubleshoot basic equipment issues and escalate concerns as appropriate.
  • Follow contamination control and containment strategies to maintain a compliant GMP manufacturing environment.
  • Participate in assigned customer Aseptic Process Simulations (APS).
  • Complete GMP documentation accurately, thoroughly, and in a timely manner.
  • Review manufacturing batch records (MBRs) and related GMP documentation as required.
  • Adhere to all safety policies, procedures, and applicable regulations.
  • Identify, document, and communicate deviations from standard procedures and accepted practices.
  • Provide accurate information and support during process deviation investigations.
  • Follow production schedules and execute assigned manufacturing activities efficiently.
  • Collaborate effectively with Manufacturing, Quality Assurance, Quality Control, and other site functions to support operational objectives.
  • Perform additional duties as assigned in support of manufacturing operations.

What we are looking for:
  • High school diploma or equivalent required; Associate degree in a scientific or technical discipline preferred.
  • 1-2 years of experience working with cell therapy technologies or related biopharmaceutical manufacturing processes in a cGMP environment.
  • Working knowledge of aseptic processing principles and cleanroom operations.
  • Ability to perform aseptic manipulations while maintaining product and environmental integrity.
  • Ability to read, understand, and follow SOPs, manufacturing instructions, and production schedules.
  • Understanding of cGMP requirements and the importance of regulatory compliance.
  • Experience completing GMP documentation and reviewing manufacturing records is preferred.
  • Proficiency with Microsoft Office applications, including Excel; experience with SAP and LIMS is desirable.
  • Strong organizational, time management, and prioritization skills.
  • Effective verbal and written communication skills.
  • Ability to work collaboratively within a team environment and resolve issues professionally.
  • Self-motivated, solution-oriented, and committed to operational excellence.
  • Ability to perform aseptic gowning on a routine basis.
  • Ability to stand for extended periods, up to 6 hours.
  • Ability to routinely lift up to 50 pounds.

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 shape the future of life sciences? Apply now.

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US