Duties: The GMP Core Director will assume responsibilities for production of gene therapy vectors intended for use in clinical development. This individual will be responsible for design, implementation, maintenance and continuous improvement of all core operations and components such as facilities, procedures, quality assurance system, and quality controls to ensure compliance with GMP requirements as applicable to early stage clinical development. This individual will direct the day-to-day operations of the core with a primary responsibility to lead manufacturing and quality assurance/quality control teams, communicate with clients, sponsors, and business managers and provide necessary support for investigational drug applications and regulatory submissions. GMP Core director will report directly to the CAROT Center Director.

Qualifications: The minimum of a Master's degree and 5 to 7 years of experience or an equivalent combination of education and experience required. PhD strongly preferred.

Reference Number: 40-30708

Salary Grade: 030

Employment Type: Exempt

Org: OP-Ophthalmology

Special Requirements:

Job Family: B-Executive/Managerial Administration