Research Associate III

LonzaHouston, TX
Onsite

About The Position

In this role, you will support the development of innovative cell therapy processes by conducting experiments, analyzing results, and contributing to process development activities.

Requirements

  • Bachelor’s or master’s degree in Bioengineering, Chemical Engineering, or related field with 2–4 years of experience in bioprocessing or cell therapy development
  • Strong hands-on experience with cell therapy manufacturing and process development, including pluripotent stem cells (iPSC), mesenchymal stem cells (MSC), hematopoietic stem cells (HSC), immune cells, and other primary cell types.
  • Demonstrated expertise in closed aseptic processing, including sterile welding, sealing, tubing assemblies, sampling, and contamination control practices.
  • Proficiency in sterile cell culture techniques and routine manipulation of mammalian cell cultures within controlled environments.
  • Experience with GMP documentation, technical writing, strong verbal and written communication skills, and statistical data analysis
  • Ability to manage multiple priorities in a fast-paced environment with strong agility

Nice To Haves

  • Bioreactor experience is a plus
  • Experience operating single-use bioprocessing equipment and unit operations such as perfusion, continuous centrifugation, automated magnetic cell separation, buffer exchange, and volume reduction.
  • Experience designing experiments, performing statistical data analysis, and interpreting process performance data.
  • Strong technical documentation, data reporting, and presentation skills within regulated development or manufacturing environments.
  • Experience working within cGMP environments and collaborating across Manufacturing, Quality, Analytical, and Project Management functions.

Responsibilities

  • Conduct experiments
  • Analyze results
  • Contribute to process development activities
  • Operate single-use bioprocessing equipment and unit operations such as perfusion, continuous centrifugation, automated magnetic cell separation, buffer exchange, and volume reduction.
  • Perform sterile cell culture techniques and routine manipulation of mammalian cell cultures within controlled environments.
  • Design experiments, perform statistical data analysis, and interpret process performance data.
  • Create strong technical documentation, data reporting, and presentation skills within regulated development or manufacturing environments.
  • Work within cGMP environments and collaborate across Manufacturing, Quality, Analytical, and Project Management functions.

Benefits

  • Relocation assistance is available for eligible candidates and their families, if needed.
  • An agile career with opportunities for professional growth
  • A collaborative and inclusive workplace culture
  • Competitive compensation that rewards performance
  • Medical, dental, and vision insurance
  • Generous paid time off and holiday programs
  • Access to learning and development resources
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