Manager/Senior Manager, CMC Quality Control

Role Summary The Manager/Senior Manager, CMC Quality Control (QC) is responsible for providing strategic and operational oversight of QC activities supporting Lexeo's gene therapy programs. This role serves as a QC lead for external contract testing laboratories (CTLs), analytical lifecycle management (i.e., late-phase method validation), stability programs, release testing support, and analytical investigation activities. The individual will work closely with Analytical Development, Technical Operations, Regulatory Affairs, Quality Assurance, and external partners to ensure analytical methods, specifications, and testing programs support clinical development, process validation readiness, and future commercial requirements. This position requires technical expertise in analytical testing, preferably of AAV-based products, as well as demonstrated experience overseeing external laboratories and driving cross-functional CMC initiatives.

Lead QC oversight of external contract testing laboratories supporting release, characterization, validation, comparability, and stability testing activities

Support product specification lifecycle management, including establishment, justification, trending, revision, and regulatory impact assessment

Partner with Analytical Development and Technical Operations to support method qualification, validation, transfer, verification, and continued performance monitoring across testing laboratories

Serve as QC subject matter expert for laboratory investigations, including OOS, OOT, atypical results, assay failures, and method performance events

Support reference standard qualification, lifecycle management, and analytical comparability initiatives

Provide technical oversight for method transfers, comparability assessments, and laboratory readiness

Collaborate with Regulatory Affairs and CMC teams to author and review regulatory submissions, responses to health authority inquiries, technical reports, and analytical sections of INDs, BLAs, and other global filings

Prepare and manage sample submission paperwork for external contract testing labs (CTLs), including quotes, purchase orders, shipping documents

Coordinate shipment of samples, reference standards, and reagents to and from manufacturing sites, external vendors, and CTLs in compliance with storage and shipping requirements

Collaborate with cross-functional CMC teams to align on sample submission and testing needs

Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Biotechnology); advanced degree (MS) a plus

6+ years of experience or 4+ with Master’s (Sr. Manager level: BS with 8+ years or MS with 6+ years experience) in Quality Control, Analytical Development, Manufacturing Sciences, Quality Assurance, or related CMC functions within biotechnology or pharmaceutical organizations

Experience supporting late-stage development, process validation, and/or commercial readiness activities preferred

Experience supporting biologics, cell therapy, gene therapy, or other advanced therapeutics preferred

Strong understanding of cGMP regulations and global regulatory expectations applicable to analytical testing and Quality Control

Experience with analytical method lifecycle management, including qualification, validation, transfer, verification, and continued performance monitoring

Knowledge of analytical techniques commonly used for AAV and biologic products (i.e., ddPCR, cell-based potency, ELISA/immunoassays, residual impurities, compendial safety testing)

Strong understanding of analytical control strategy development and specification management

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