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Process Engineer Cell Therapy Jobs in Texas (NOW HIRING)

$13.75 - $17.75/hr

The Cell Therapy Technologist I is required to document each step of a process and/or procedure per the facility's standard operating procedures and policies. The Cell Therapy Technologist I complies ...

New

Manufacturing Supervisor - Cell Therapy

Houston, TX · On-site

$57K - $78K/yr

Coordinate activities across Manufacturing, Quality, Engineering, and other support teams to ensure ... Solid understanding of production process flow, batch documentation, and quality systems in a ...

Manufacturing Supervisor - Cell Therapy

Houston, TX · On-site

$57K - $78K/yr

Coordinate activities across Manufacturing, Quality, Engineering, and other support teams to ensure ... Solid understanding of production process flow, batch documentation, and quality systems in a ...

The Process Engineer is responsible for leading advanced process development across the full ... Support molding cell development and execution * Support EOAT design and fabrication * Manage mold ...

The Process Engineer is responsible for leading advanced process development across the full ... Support molding cell development and execution * Support EOAT design and fabrication * Manage mold ...

The Process Engineer is responsible for leading advanced process development across the full ... Support molding cell development and execution * Support EOAT design and fabrication * Manage mold ...

The Process Engineer is responsible for leading advanced process development across the full ... Support molding cell development and execution * Support EOAT design and fabrication * Manage mold ...

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Process Engineer Cell Therapy information

What does a Process Engineer in Cell Therapy do?

A Process Engineer in Cell Therapy is responsible for developing, optimizing, and overseeing the manufacturing processes used to produce cell-based therapies. They ensure that processes are efficient, scalable, and compliant with regulatory standards, while maintaining the quality and safety of the final product. Their work often involves collaborating with scientists, quality teams, and production staff to troubleshoot issues and implement improvements. Process Engineers in this field play a crucial role in bringing innovative cell therapies from the laboratory to clinical and commercial production.

What are the key skills and qualifications needed to thrive as a Process Engineer in Cell Therapy, and why are they important?

To thrive as a Process Engineer in Cell Therapy, you need a strong background in chemical or biomedical engineering, experience with cell culture processes, and often a relevant degree. Familiarity with GMP regulations, bioprocessing equipment, and quality control systems is typically required, along with experience using tools like bioreactors and analytical software. Excellent problem-solving, communication, and project management skills help you collaborate effectively and drive process improvements. These skills ensure the development and optimization of safe, scalable, and compliant cell therapy manufacturing processes.

What is the difference between Process Engineer Cell Therapy vs Process Engineer Bioprocess?

AspectProcess Engineer Cell TherapyProcess Engineer Bioprocess
CredentialsBachelor's/Master's in Bioengineering, Chemical Engineering, or related fieldsBachelor's/Master's in Bioengineering, Chemical Engineering, or related fields
Work EnvironmentCell therapy manufacturing facilities, GMP labsBiopharmaceutical production plants, GMP facilities
Industry UsageCell therapy companies, biotech firmsBiotech, pharmaceutical manufacturing
Common Search/ComparisonYesYes

Process Engineer Cell Therapy and Process Engineer Bioprocess roles share similar educational backgrounds and work environments, often within GMP manufacturing settings. The main difference lies in their focus: cell therapy engineers specialize in developing and scaling processes for cellular treatments, while bioprocess engineers work on broader biopharmaceutical production. Both roles are essential in biotech industries and often overlap in skills and certifications.

What are some typical challenges faced by Process Engineers in Cell Therapy manufacturing, and how are they addressed?

Process Engineers in Cell Therapy often encounter challenges such as scaling up production from clinical to commercial scale while maintaining stringent quality standards and regulatory compliance. Managing variability in biological materials and ensuring consistency across batches is another common hurdle. These challenges are typically addressed through robust process development, close collaboration with quality and manufacturing teams, and implementation of automation and data-driven process controls. Continuous training and adaptation to evolving regulatory guidelines also play a key role in overcoming these obstacles.
What job categories do people searching Process Engineer Cell Therapy jobs in Texas look for? The top searched job categories for Process Engineer Cell Therapy jobs in Texas are:
What cities in Texas are hiring for Process Engineer Cell Therapy jobs? Cities in Texas with the most Process Engineer Cell Therapy job openings:
Cell Therapy Technologist I

Cell Therapy Technologist I

Moffitt

On-site

$13.75 - $17.75/hr

Full-time

Posted 7 days ago

New


Job description

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times' Top Workplaces.

Summary

The Cell Therapy Technologist I, working with minimal supervision, will be responsible for performing cellular product processing using multiple processing and separation techniques. The Cell Therapy Technologist I is able to perform qualitative and quantitative assays on cell therapy products. Performed duties must adhere to aseptic technique when involving any cellular product production. The Cell Therapy Technologist I is required to document each step of a process and/or procedure per the facility's standard operating procedures and policies. The Cell Therapy Technologist I complies to the facility's standard operating procedures and policies which incorporate the cGMP/ cGTP, FACT, CAP and AABB regulatory standards applicable to cellular therapy product production and analysis. Must be trained and proficient in 5 or more technologist processes according to the Cell Therapy Training procedure. Must demonstrate the ability to gather data for the management team and project leaders.

Position Highlights:

  • Opportunity to join a NCI designated comprehensive cancer center in production of novel cellular therapy treatments for cancer patients
  • Participation in cutting edge adoptive cellular therapy treatments which include the culture and activation of immune cells to return to patients
  • Develop and perform assays on cellular products for safety and function
  • Involvement in the rapidly growing multiple clinical trials within the cell therapy area.

The Ideal Candidate

  • Experience in cell culture and aseptic technique.
  • Working knowledge of Adoptive Cell Therapy
  • Understanding of good documentation practices and requirements
  • The successful candidate will be a strong communicator, engaged, and will work closely with members of the Cell Therapy Team.
  • Exhibit interest and excitement in participating in the production of cellular products
  • Proficiency in ELISA, qPCR, Flow cytometry, and automated cell counting methods.

Responsibilities:

  • Working with minimal supervision, perform cellular product processing using multiple processing, cell culture, and separation techniques.
  • Complete qualitative and quantitative assays on cell therapy products including flow cytometry, qPCR and ELISA.
  • Comply with the facility's standard operating procedures and policies which incorporate the cGMP/cGTP, FACT, CAP and AABB regulatory standards applicable to cellular therapy product production and analysis.
  • Identify problems that may adversely affect product or testing performance and follow the Cell Therapies Facility standard operating procedures and policies whenever productprocessing or analytic testing are not within the defined acceptable criteria and/or levels of performance.
  • Handle fresh and frozen cellular products for shipment and infusion.
  • Maintain aseptic technique and work within a clean room environment.
  • Other duties as assigned.

Credentials and Qualifications:

  • Bachelor's Degree in Medical Technology or other Biological Science.
  • One or more years of cell therapy or related experience.
  • Demonstrated competency in diverse biological processes following good documentation practices.
  • Demonstrated ability to work independently to achieve expectedoutcomes

Salary Range

Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.


We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.

Moffitt Career Site

If you have the vision, passion, and dedication to contribute to our mission,then we have a place for you!

1. Equal Employment Opportunity

Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.

2. Reasonable Accommodation

Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email atHRReceptionists@moffitt.org. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.

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