Providing functional, high-purity recombinant proteins—including membrane proteins and nanodiscs—to overcome bottlenecks in drug screening and target validation.
Harness the power of protein degraders for precise protein degradation, expanding druggable targets and enhancing therapeutic effectiveness for cutting-edge drug discovery.
RNA design, synthesis, and manufacturing—covering mRNA, saRNA, circRNA, and RNAi. Fast turnaround, rigorous QC, and seamless transition from research to GMP production.
Balancing accuracy, accessibility, affordability, and rapid detection to safeguard public health and strengthen global response to infectious diseases.
Stable expression over 15 generations with rapid cell line development in just 3 months. Supports adherent and suspension cell lines, offering MCB, WCB, and PCB establishment.
Scalable mRNA production from milligrams to grams, with personalized process design for sequence optimization, cap selection, and nucleotide modifications, all in one service.
Leverage AI to uncover hidden high-potential small molecules, prioritize leads intelligently, and reduce costly trial-and-error in early drug discovery.
Our promise to you: Guaranteed product quality, expert customer support.
24x7 CUSTOMER SERVICE
CONTACT US TO ORDER
Scientist, Cell Therapy/Gene Therapy
Key Responsibilities:
Drive the research into new therapies, such as cell and gene therapy, at the interface of cell engineering into bioprocessing production.
Execute the translation of new biological molecular tools into bioprocessing applications such as CRISPR tools for improved cell performance in combination with microfluidic & automation approaches.
Identify and establish collaborations with world-leading academics and startup companies for cutting-edge technology concepts.
Guide and provide practical support for completion of proof-of-concept experimental evaluations.
Drive and support potential prototype technology design.
Basic Qualifications:
Ph.D. in molecular biology, cellular biology, stem cell biology, biomedical engineering, or closely related fields with experience with biological cellular systems.
Have established both a foundationally theoretical and practical competency in cell or gene therapy that is internationally recognized through publications and presentations.
A practical competency in cell or gene therapy technologies such as viral and non-viral delivery systems.
A practical competency in cell therapy experience such as in vitro stem cell (HSC/iPSC/ESC) culture and/or T-cell differentiation systems, and T-cell culture.
Preferable to have experience in cell engineering using viral or non-viral methods, for gene therapy.
A desire for miniaturization and automation that will lead to the development of next-generation personalized automated workflows.
Ability to prioritize tasks and balance individual technical contribution with coordination of fast-paced research activities across multiple sites, organizations, and disciplines.
Creative Biogene is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status.