GxP Quality Lead en Lexeo Therapeutics

Lexeo is building the future of cardiac genetic medicine, and we’re looking for a bold, strategic leader to help us get there. As a Senior Director or Vice President, GxP Quality, you will lead the charge in scaling our Quality organization across clinical and commercial manufacturing programs, embedding excellence into every step of our journey from development to commercial launch. You’ll architect a globally compliant, phase-appropriate GxP strategy that empowers innovation while ensuring rigor. You’ll shape systems, guide teams, and drive decisions that keep science at the center and quality at the forefront. This is your opportunity to lead with purpose, influence across functions, and build a culture where accountability, collaboration, and continuous improvement thrive. If you’re energized by challenges, inspired by impact, and ready to help set a new standard in genetic medicine, this is your moment.  Lexeo is seeking an experienced and hands-on senior leader of  GxP Quality to be accountable for both leading and operationalizing strategy to scale our Quality organization across clinical development, manufacturing, translational sciences and clinical biomarkers . This individual will be responsible for developing a phase-appropriate, scalable GxP Quality strategy, ensuring compliance with global regulatory standards (e.g., FDA, EMA, ANVISA, ICH), and embedding a culture of operational excellence across the company.  The ideal candidate will bring deep GMP and GCP expertise, strong leadership and communication skills, and the ability to thrive in a fast-paced, development-stage environment while providing strategic oversight and pragmatic solutions that enable innovation. 



Key Responsibilities

Develop and execute a scalable GxP Quality Assurance strategy aligned with Lexeo’s business goals and regulatory expectations. 

Serve as the senior Quality leader across GMP, GCP, GLP, and GVP functions. 

Advise executive leadership on quality risks, mitigation strategies, and inspection readiness. 

Foster a proactive quality culture rooted in continuous improvement, accountability, and operational excellence. 

Build, mentor, and develop a high-performing Quality team that reflects Lexeo’s values of scientific rigor and collaboration 

Establish and maintain a phase-appropriate Quality Management System (QMS) establishing a document hierarchy including a Quality Manual, policies, SOPs and other documents needed to support a virtual gene therapy organization with early and late stage programs. And, also enabling a QMS that can support a registrational study and commercial launch. 

Ensure quality systems effectively support clinical development, pharmacovigilance, all CMC activities, translational sciences, clinical biomarker development, and external partnerships 

Oversee implementation and maintenance of an electronic QMS (eQMS) to support scalability and compliance 

Lead and/or provide leadership support for GCP, GLP, GMP and GVP quality activities, including internal and external audits, vendor oversight, deviation investigations, and quality agreements, health authority inspections. 

Support clinical trial operations by ensuring all aspects of ICH GCP are followed (e.g., protocol adherence, data integrity, and informed consent compliance) 

Oversee early and late phase manufacturing QA activities, including batch record review, product release, and disposition in collaboration with CMC and Technical Operations 

Drive inspection readiness and represent Lexeo during regulatory inspections and partner audits 

Establish procedures for surveying regulatory intelligence and disseminate throughout Lexeo. 

Oversee and management of a risk-based vendor qualification program including performance of external audits, and ongoing compliance monitoring of CROs, CDMOs, testing laboratories, and other GxP service providers 

Ensure robust Quality Agreements and alignment of standards and expectations across all external partners 

Partner closely with Clinical Development, Regulatory Affairs, Technical Operations, Supply Chain, and Research to ensure quality is embedded throughout the product lifecycle 

Serve as the QA representative on governance bodies and cross-functional development teams, ensuring risk-based decision-making and clear communication of quality principles 

Qualifications

Bachelor’s degree in a relevant scientific discipline (Biology, Chemistry, Engineering, or related field); advanced degree preferred 

12–15+ years of experience in Quality Assurance within the biotech or pharmaceutical industry, with significant exposure to both GMP and GCP environments 

Proven leadership in building and scaling GxP quality systems within a clinical- to commercial-stage setting 

Strong knowledge of FDA, EMA, and ICH regulations and inspection practices 

Experience in regulatory submissions, from IND to BLA, in support of CMC and clinical components 

Experience managing audits, CAPAs, deviations, and regulatory inspections 

Demonstrated success leading external partnerships (CROs, CDMOs) 

Excellent communication, collaboration, and problem-solving skills with the ability to influence across functions and levels 

Strategic thinker who can balance regulatory rigor with Lexeo’s innovative, fast-paced biotech environment 

Preferred Experience

Experience with AAV-based gene therapy or biologics 

Familiarity with global clinical trial operations and pharmacovigilance practices 

Proven ability to lead cross-functional quality teams in a growth-stage organization 

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