Oversee commercial GMP lentiviral vector manufacturing at the CDMO, including campaign readiness, batch record review, deviations, CAPAs, change controls, and starting materials. Coordinate with internal and CDMO teams to support reliable supply, regulatory compliance, performance improvement, and inspection readiness. Requires a bachelor’s degree in engineering, life sciences, or a related field, with an advanced degree preferred, and at least six years of biopharma manufacturing experience, including three years in a leadership or supervisory role. Candidates should bring GMP manufacturing and quality-system experience, preferably in viral vectors or cell and gene therapy, along with CDMO oversight and strong cross-functional leadership skills.
Genetix Biotherapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
