Senior Director, IDMO Site Quality
CellaresNew Jersey, United States • South San Francisco, California, United States
Posted September 29, 2025
90000 - 210000 USD year
Full Time
About the Company
Cellares is an Integrated Development and Manufacturing Organization (IDMO) specializing in Industry 4.0 technologies for cell therapy manufacturing. The company develops the Cell Shuttle, a flexible, high-throughput platform that automates the entire manufacturing process, enabling academic, biotech, and pharma partners to accelerate drug development, reduce costs, and meet global patient demand. Headquartered in South San Francisco with a commercial-scale Smart Factory in Bridgewater, New Jersey, Cellares is backed by over $355 million in financing from world-class investors.
Job Description
Cellares is seeking a highly motivated Senior Director of IDMO Site Quality to lead the Quality organization within a cGMP-compliant facility. The role involves ensuring patient safety and compliance during cell therapy manufacturing. The ideal candidate will have extensive experience in a cGMP environment and will drive collaboration between QA/QC, Operations, and other functional areas. This is a multidisciplinary role requiring strategic leadership and experience with process controls.
Requirements
- Bachelor's degree in science, engineering, or related field
- 10+ years of Quality Management experience within a cGMP environment
- Cell/Gene Therapy and CDMO experience preferred
- US FDA and other regulatory agency experience
Benefits
- Competitive base salaries
- 401k Matching
- Onsite lunches
- Stock options
