Responsibilities: for the Sr. Research Associate, Process Development include: · Design and Execute process development studies supporting the optimization and standardization of pluripotent stem cell-derived cell therapy manufacturing processes · Utilize expertise in qPCR and Flow Cytometry to assess laboratory assays for scale up and tech transfer · Perform hands-on human pluripotent stem cell/iPSC culture and differentiation activities · Support the development of robust, reproducible, scalable, and GMP-ready processes for future clinical manufacturing. · Execute experiments designed to evaluate and optimize process parameters, culture conditions, raw materials, reagents, and differentiation methods. · Support activities associated with process scale-up, process characterization, and eventual technology transfer to a CDMO. Qualifications: for the Sr. Research Associate, Process Development: A minimum of 3+ years of pharmaceutical research and process development Hands-on experience withs Stem cell/iPSC culture and differentiation 1-3+ years of experience supporting cell therapy process development, scale-up, process characterization, or technology transfer. 1-3+ years of experience working in or supporting processes transitioning from research/preclinical development toward GMP manufacturing. Bachelor's or Master's Degree in in Scientific field Compensation: for the Sr. Research Associate, Process Development include: Salary Range is $85,000 - $105,000 dependent upon experience Comprehensive benefits package
| Location | Cambridge, MA |
| Salary | $85,000–$105,000 Per Year |
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