The successful candidate will be responsible for the formulation and Drug Product (DP) process development of clinical candidates, design and execution of process characterization/validation studies, leading technical process transfer to internal and external manufacturing sites in support of clinical trials of Catamaran programs. The scientist will be responsible for authoring and reviewing technical reports and sections for regulatory submissions. The scientist will collaborate extensively with research, process and product development, regulatory, CMC and clinical teams.
This position requires BS or MS in bioengineering, chemical engineering, biochemistry, chemical biology, biology, biophysics, pharmaceutical sciences, or equivalent/related disciplines with 2-5 years of relevant experience in cell cryopreservation, cell biology, and/or analytical development in academia or the cell therapy industry.
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