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. 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.
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
Requirements
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.
Experience operating single-use bioprocessing equipment and unit operations such as perfusion, continuous centrifugation, automated magnetic cell separation, buffer exchange, and volume reduction.
Proficiency in sterile cell culture techniques and routine manipulation of mammalian cell cultures within controlled environments.
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.
About Lonza
We are committed to fostering an inclusive workplace and providing equal opportunities to all qualified applicants.
Ready to shape the future of life sciences?
Benefits
Dental insuranceVision insurance
Additional Information
Research Associate III
Location: Pearland, TX, USA
Relocation assistance is available for eligible candidates and their families, if needed.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there is no single way of doing things. Our greatest strength is our people working together to develop ideas that help businesses help people. In return, we empower our teams to own their careers and make a meaningful impact on the world.
In this role, you will support the development of innovative cell therapy processes by conducting experiments, analyzing results, and contributing to process development activities.
What you will get
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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