Associate Director Downstream Process Development
Location: Bedford, MA
The successful candidate will be an integral part of a fast paced and rapidly growing group of scientists and engineers developing purification processes for the manufacture of our proprietary adeno-associated virus (AAV) based gene therapy and gene editing products. Responsibilities will include helping to develop and oversee the development of multiple unit operations with an emphasis on chromatographic separations. Critical to this role is the ability to lead the end to end development of a purification process and to be able to effectively communicate results through high quality technical reports and oral presentations
Education & Experience
BS (9+ years), MS (6+) or PhD (3+) years of directly related experience. Degree emphasis in Chemical Engineering, Biochemistry, Bioengineering, or related discipline preferred.
Homology Medicines, Inc. (HMI) has built foundational intellectual property on gene editing and gene therapy vectors derived from naturally occurring human adeno-associated viruses (AAVs). The Company's technology is precise, on-target and highly efficient for in vivo editing of genetic mutations. This transformative platform technology, combined with an elite leadership team of biopharmaceutical industry veterans, create a significant opportunity for HMI to rapidly advance a diverse pipeline of new medicines that address and potentially cure the underlying cause of genetic diseases.
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