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Process Engineer Cell Therapy Jobs in Texas (NOW HIRING)

Viant

Process Engineer

San Antonio, TX · On-site

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 ...

T1 Energy Inc.

Senior Deposition Process Engineer

Austin, TX · On-site

$103K - $133K/yr

You'll be working at the leading edge of solar cell fab, owning critical deposition and thermal ... yield engineering teams. * Drive process characterization, DOE execution, and data analysis to ...

New

Lonza

Quality Control Project Lead - Cell Therapy

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Lead Quality Control activities supporting client programs through technology transfer, process ... Strong knowledge of cell therapy product development, technology transfer, analytical methods ...

Lonza

Quality Control Project Lead - Cell Therapy

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Lead Quality Control activities supporting client programs through technology transfer, process ... Strong knowledge of cell therapy product development, technology transfer, analytical methods ...

T1 Energy

Senior Diffusion Process Engineer

Austin, TX · On-site

$110 - $140/hr

You'll be working at the leading edge of solar cell fab, owning critical doping thermal processes ... Collaborate with equipment engineers and tool vendors to qualify new tool integrations, execute ...

T1 Energy Inc.

Senior Diffusion Process Engineer

Austin, TX · On-site

$103K - $133K/yr

You'll be working at the leading edge of solar cell fab, owning critical doping thermal processes ... Collaborate with equipment engineers and tool vendors to qualify new tool integrations, execute ...

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Showing results 21-40

All JobsProcess Engineer Cell Therapy JobsProcess Engineer Cell Therapy Jobs in Texas

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?

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

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

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:

Process Engineer Cell Therapy jobs near you
Infographic showing various Process Engineer Cell Therapy job openings in Texas as of June 2026, with employment types broken down into 100% Contract. Highlights an 100% In-person job distribution.

Process Engineer

Viant

San Antonio, TX • On-site

Full-time

Re-posted 18 days ago

Job description

About the company:
Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With nearly 6,000 employees across 24 locations worldwide, it delivers high-quality, life-enhancing products with the scale and expertise to bring devices to market efficiently. Learn more at Viant Medical's website or on LinkedIn.
About the role:
The Process Engineer is responsible for leading advanced process development across the full lifecycle of molding and manufacturing programs, applying expert scientific molding and cavity pressure control principles to deliver robust, optimized processes. This role provides hands-on technical leadership for tooling design, process validation (IQ, OQ, PQ), and DOE execution, while supporting NPI, sustaining engineering, and business development initiatives. The Principal Process Engineer serves as a key technical interface between Viant, customers, tool shops, and internal teams to ensure regulatory compliance and best-in-class production outcomes.
  • Work Model: Remote
  • Travel Requirement: 75% travel across Viant locations in the US but mainly to Costa Rica, Tijuana, BC, and Vega Baja, PR sites.

What you'll do:
  • Lead the process development cycle
  • Evaluate processes for robustness, accuracy, and optimization
  • Initiate improvement projects
  • Quality/Metrology support: Assist site QE on KPI/KPO impacting part quality and process control
  • Partner with GTS/Site Tooling Engineer on design requirements
  • Partner with Tool Engineer on design and development requirements
  • Support business development by selling tooling solutions and resolving processing issues
  • Support corrective actions, re-validations, and tool/process optimization
  • Oversee process development through I.Q. and O.Q. runs; report required
  • Complete other related projects and tasks assigned
  • Demonstrate expert knowledge and performance
  • Apply scientific molding (Decoupled 2 and Decoupled 3)
  • Expert in cavity pressure monitoring and control (RJG)
  • Join technical reviews with customers and mold shops
  • Support DFM and tool design reviews with Tool Engineers
  • Support molding cell development and execution
  • Support EOAT design and fabrication
  • Manage mold shop deliverables and expectations (SIM reports)
  • Confirm receiving-site requirements (press/shot size/tonnage/special sequence) and machine capability studies
  • Develop processes, review Moldflow data for start-up and debug
  • Travel to customer sites, tool shops, and Viant facilities as needed; trip report required
  • Prepare, track, and communicate Process DOEs, report results and recommendations
  • Manage multiple concurrent projects (minimum 20 active)

Requirements:
Education:
  • Bachelor of Science Degree in Engineering or related plastics discipline or 4-year engineering degree or equivalent completion of a 4,000 hour or 2-year process engineering apprenticeship.
  • Certification from a school in advanced molding or RJG Master Molder 2 (or equivalent).
  • Certification in Basic Mold Flow (or equivalent) is a plus.
  • Certification in Master Molding 3 is a plus.

Years of Experience:
  • 10+ years of experience in processing and in a molding environment, process development, qualification, validation of molds, etc.

Job Knowledge :
  • Extensive knowledge and able to train in: processing and process development techniques in scientific molding principles (MM2 skill level)
  • Plastics-Injection Molding; LSR (preferred)
  • Excel, PowerPoint, Word, and general computer skills; SolidWorks (drawing); 3D printing/3D software (preferred)
  • Some knowledge in FDA, QSR, and ISO 13485 medical device regulations and standards.
  • Understanding of statistics, Cp & Cpk studies for process. I.Q., O.Q. and P.Q. requirements
  • Strong understanding of DOE methods and implementation
  • Expert knowledge of cavity pressure technologies and advanced control principles
  • Familiarity with the various engineering grade thermoplastic resins and Mold Flow analysis."

Additional Requirements:
  • Authorized to work in the U.S.
  • Spanish proficiency
  • Ability to travel up to 75% to Viant sites (U.S., Costa Rica, Tijuana, and Vega Baja, PR)

Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this through our depth and breadth of capabilities, end-to-end integration, technical expertise, and relentless focus on our customers and on operational excellence. With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small-company service and attention with big-company resources. For more information, visit viantmedical.com or follow us on LinkedIn.
Viant provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Viant complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.

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