Lexeo Therapeutics

Role SummaryThis Scientist II will independently design execute and analyze research studies and will drive one or more analytical development projects for AAV-based gene therapy programs. The role provides technical leadership in the development optimization qualification validation

Role SummaryThis Scientist II will independently design execute and analyze research studies and will drive one or more analytical development projects for AAV-based gene therapy programs. The role provides technical leadership in the development optimization qualification validation

Role SummaryThe Manager/Senior Manager CMC Quality Control (QC) is responsible for providing strategic and operational oversight of QC activities supporting Lexeos gene therapy programs. This role serves as a QC lead for external contract testing laboratories (CTLs) analytical lifecyc

Role SummaryThe Manager/Senior Manager CMC Quality Control (QC) is responsible for providing strategic and operational oversight of QC activities supporting Lexeos gene therapy programs. This role serves as a QC lead for external contract testing laboratories (CTLs) analytical lifecyc

Role SummaryWe are seeking an experienced Associate DirectorQualitySystems& Compliance to lead strategic oversight and continuous improvement of our Quality Management System (QMS) Document Control for Policies SOPs Work Instruction & forms and GxP as well as some non GxP Training pro

Role SummaryWe are seeking an experienced Associate DirectorQualitySystems& Compliance to lead strategic oversight and continuous improvement of our Quality Management System (QMS) Document Control for Policies SOPs Work Instruction & forms and GxP as well as some non GxP Training pro

Role SummaryWe are seeking an experienced Associate DirectorQualitySystems& Compliance to lead strategic oversight and continuous improvement of our Quality Management System (QMS) Document Control for Policies SOPs Work Instruction & forms and GxP as well as some non GxP Training pro

Role SummaryWe are seeking an experienced Associate DirectorQualitySystems& Compliance to lead strategic oversight and continuous improvement of our Quality Management System (QMS) Document Control for Policies SOPs Work Instruction & forms and GxP as well as some non GxP Training pro

RoleSummaryThe Senior Scientist supports development optimization and scale-up of AAV manufacturing processes using Sf9/baculovirus and HEK-based systems. This role contributes toearly andlate-stage CMC activities including process characterization technology transfer control strategy

RoleSummaryThe Senior Scientist supports development optimization and scale-up of AAV manufacturing processes using Sf9/baculovirus and HEK-based systems. This role contributes toearly andlate-stage CMC activities including process characterization technology transfer control strategy

RoleSummaryThe Senior Scientist I supports development optimization and scale-up of AAV manufacturing processes using Sf9/baculovirus and HEK-based systems. This role contributes to early and late-stage CMC activities including process characterization technology transfer control stra

RoleSummaryThe Senior Scientist I supports development optimization and scale-up of AAV manufacturing processes using Sf9/baculovirus and HEK-based systems. This role contributes to early and late-stage CMC activities including process characterization technology transfer control stra

Role SummaryTheSenior DirectorReal World Evidenceand Health Economics and Outcomesis responsible forprovidingscientific inputduring protocol development study design oversight ofclinical aspects ofstudy conduct and interpretation of study results through the final study report.The can

Role SummaryTheSenior DirectorReal World Evidenceand Health Economics and Outcomesis responsible forprovidingscientific inputduring protocol development study design oversight ofclinical aspects ofstudy conduct and interpretation of study results through the final study report.The can