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Cell Therapy Process Development Jobs in Texas (NOW HIRING)

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Core Technician - Cell Therapy Location: This is an on-site position located in Houston, TX. As a ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

Posted Job Advert Core Technician - Cell Therapy Location: This is an on-site position located in ... This position is responsible for performing aseptic cell processing activities, operating ...

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Showing results 21-40

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Cell Therapy Process Development information

What is cell therapy process development?

Cell Therapy Process Development refers to the design, optimization, and scaling up of manufacturing processes for cell-based therapies, such as CAR-T cells or stem cell products. Professionals in this field work on translating laboratory research into reproducible, efficient, and safe production methods that meet regulatory standards. This involves working with cell culture techniques, bioreactors, quality control, and process validation to ensure that therapies can be produced consistently for clinical and commercial use. The goal is to develop robust processes that deliver safe and effective cell therapies to patients.

What are the key skills and qualifications needed to thrive as a cell therapy process development professional?

To thrive in Cell Therapy Process Development, you need a solid background in cell biology, biotechnology, or a related field, often supported by a relevant degree and experience with cell culture techniques. Familiarity with bioprocessing equipment, Good Manufacturing Practice (GMP) regulations, and analytical tools such as flow cytometry and PCR is typically required. Strong problem-solving skills, attention to detail, and effective teamwork enhance performance in this collaborative and innovative environment. These competencies ensure the safe and efficient development of cell therapies, meeting rigorous quality standards and advancing clinical applications.

What are some typical challenges faced by professionals in cell therapy process development, and how are they addressed?

Professionals in Cell Therapy Process Development often encounter challenges such as scaling up production processes from laboratory to clinical or commercial scale while maintaining product quality and consistency. Additional hurdles include adhering to strict regulatory requirements and managing complex collaborations across cross-functional teams, like quality assurance, regulatory affairs, and manufacturing. These challenges are typically addressed through rigorous process optimization, thorough documentation, and ongoing communication with stakeholders to ensure that all aspects of the process meet industry standards and regulatory expectations.

What is the difference between Cell Therapy Process Development vs Cell Therapy Manufacturing Specialist?

AspectCell Therapy Process DevelopmentCell Therapy Manufacturing Specialist
CredentialsTypically requires a degree in biology, biochemistry, or biomedical engineering; certifications in GMP or cell therapy are commonSimilar credentials; often holds degrees in related fields and GMP certifications
Work EnvironmentResearch labs, development facilities, early-stage process optimizationManufacturing plants, production floors, quality control labs
Industry UsageFocuses on developing and optimizing cell therapy processesInvolved in large-scale production and process execution

Cell Therapy Process Development professionals focus on designing and refining cell therapy procedures, while Cell Therapy Manufacturing Specialists handle the production and quality assurance in manufacturing settings. Both roles require similar educational backgrounds and certifications but differ mainly in their work environment and specific responsibilities.

What are popular job titles related to Cell Therapy Process Development jobs in Texas?

For Cell Therapy Process Development jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Cell Therapy Process Development jobs in Texas look for?

The top searched job categories for Cell Therapy Process Development jobs in Texas are:

What cities in Texas are hiring for Cell Therapy Process Development jobs?

Cities in Texas with the most Cell Therapy Process Development job openings:

Cell Therapy Process Development jobs near you
Infographic showing various Cell Therapy Process Development job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

Manufacturing Supervisor (Cell Therapy CDMO)

The Woodlands, TX • On-site

Cellipont Bioservices
Biotechnology Research and Development • 51 - 200 employees
Learn more about Cellipont Bioservicesexternal

$55K - $75K/yr

Full-time

Medical, Retirement, PTO

Re-posted 8 days ago

Job description

"Bridging Innovation to Cure
"Developing and manufacturing your cell therapies from benchtop to bedside"
Summary
Cellipont Bioservices is growing, and we are looking for a Manufacturing Supervisor who believes in the potential bridging of client's discoveries to patient cures and who want to challenge the status quo and take Cellipont and its clients to the next level.
The Manufacturing Supervisor will provide hands-on direction for manufacturing personnel and activities. This position requires extensive technical expertise in aseptic techniques. Provide expertise in writing/reviewing SOPs, Batch Records, Deviations, CAPA's and other technical document/compliance documents as it relates to the Manufacturing Operations. The Manufacturing Supervisor is also responsible for ensuring all personnel activities are executed timely and cost effectively to ensure customer and stakeholder satisfaction. This role will also require the individual to demonstrate strong customer service capability, ability to work cross-functionally and possess strong leadership skills.
The Role
  • Oversee and schedule the manufacturing operations and personnel
  • Leads a manufacturing team to identify issues and propose adequate solutions
  • Responsible for training manufacturing personnel on the use of the Batch records, scheduling, ordering of raw materials, components and supplies, setting up production batches, and maintaining inventory
  • Ensure batches adhere to established Quality standards
  • GMP batch review and close-out with Quality Assurance group
  • Conduct interviews and provide input for hiring new manufacturing specialist.
  • Provide daily production updates to production managers, client representatives, and project managers
  • Provide guidance for continuous improvement initiatives within the Manufacturing team
  • Represent the department to clients and on cross-functional project teams
  • May operate production equipment and inspect, label, or package products
  • Work with Manufacturing, Quality, Engineering and Technology groups on issues and identifies process improvement opportunities
  • Ensure the completeness and accuracy of manufacturing documentation per approved procedures.
  • Identify and support the implementation of process efficiencies and areas for improvement
  • Ensures solutions are consistent with organization's objectives
  • Responsible for establishing performance standards, employee coaching and development, determining employee responsibilities, evaluating performance and rewarding as appropriate
  • Perform additional duties as needed

The Candidate
  • Bachelor's Degree - Life Sciences or Chemical Engineering and minimum 5 - 7 years in GMP environment with experience in GMP manufacturing operations/Cell Therapy/Human Cell Cultivation. CDMO experience preferred.
  • 3 years minimum of leadership/management experience in a GMP environment
  • Experience in writing, executing and reviewing SOPs / MBRs while maintaining proper GDP guidelines.
  • Good mechanical aptitude, familiar with general equipment associated with Cell and Gene Therapy Processing.
  • Detail oriented and highly motivated, follow oral and written instructions, communicate effectively, think logically, and thrive independently and/or in a fast-paced team environment
  • Must be proficient in Word and Excel.
  • Ability to interpret process trends and data and react appropriately to unexpected outcomes.
  • Innovative spirit, strong initiative and work ethic, and positive attitude
  • Ability to work flexible hours and inconsistent schedules as necessary to meet production demands and timelines
  • Must be available to work 2nd shift (2:00 PM - 11:00 PM), Monday through Friday, with occasional weekend or holiday support as needed

Work Environment
  • Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities
  • Ability to work off-shift and extra hours as required
  • Weekends & Holidays as required

POSITION BENEFITS
  • Opportunities for career growth within an expanding team
  • Defined career path and annual performance review & feedback process
  • Cross-functional exposure to other areas of within the organization
  • Robust benefit package designed for unique Health & Wellness needs, including coverage for your furry family members
  • 401K strong employer match
  • Tuition Reimbursement
  • Employee Referral Bonuses
  • Flexible work schedules and PTO based on role/level, increasing 1 PTO day each year and paid holidays
  • Gain experience in the cutting-edge cell therapy space

"At Cellipont Bioservices, we look for candidates with an innate desire to serve. Our "family" approach ensures you will get the mentorship you need to develop a satisfying career here!"
Notice to Agency and Search Firm Representatives
Cellipont Bioservices is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Cellipont Bioservices employee by a third-party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Cellipont Bioservices. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.

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