Description

You will oversee the day-to-day operational performance of key contract development and manufacturing organizations (CDMOs) for Sana's cell and gene therapy programs, acting as the primary liaison between Sana Technical Operations and CDMOs to ensure timely delivery of high-quality preclinical and clinical products. You will manage budgets, support tech transfers, monitor production campaigns, and negotiate contracts.

Requirements

• Bachelor's degree with 5+ years of outsourced clinical/commercial manufacturing experience in biotech/pharma
• Knowledge of regulatory guidelines and cGMP quality systems
• Experience in early-stage clinical to commercial environments
• Strong communication, problem-solving, and relationship-building skills
• Business acumen with ability to anticipate operational issues and propose solutions

Responsibilities

• Act as primary liaison between Sana Technical Operations and CDMOs
• Ensure adherence to project schedules and implement governance structures
• Develop and oversee budgets for projects, including internal budgeting and CDMO financial performance
• Partner with technical departments to ensure successful tech transfer to CDMOs
• Monitor technical transfer and production campaigns, report on CDMO performance