Full Time

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

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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

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Full Time

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

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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

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Lexeo Therapeutics

Full Time

Role SummaryTheVice PresidentMedical Affairs will provide enterprise-level leadership acrossLexeosgene therapy to the Chief Medical Officer this rolewill set the strategic direction for Medical Affairs overseeing scientific communications congress strategy external expert engagement

Role SummaryTheVice PresidentMedical Affairs will provide enterprise-level leadership acrossLexeosgene therapy to the Chief Medical Officer this rolewill set the strategic direction for Medical Affairs overseeing scientific communications congress strategy external expert engagement

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Full Time

Role SummaryLexeo is seeking an experienced and motivated clinical development leader to advance late-stage development programs as a key member of our development team. This individual will report to the Vice President Clinical Development Cardiology and will provide strategic and ha

Role SummaryLexeo is seeking an experienced and motivated clinical development leader to advance late-stage development programs as a key member of our development team. This individual will report to the Vice President Clinical Development Cardiology and will provide strategic and ha

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