Director of Manufacturing in Cell Therapy
Neurogenesis · Posted 2026-10-20
job requirements
Director of Manufacturing in Cell Therapy
Key Responsibilities:
The primary accountability of this role is to enable the manufacturing of cell therapy
products for clinical supply, as a cell therapy technical expert for cGMP manufacturing, through providing hands-on technical leadership and operational oversight for a cell therapy manufacturing facility in Rochester, NY.
We are looking for a candidate with excellent GMP, scientific, technical communication, and leadership skills.
Specifically:
- Provide leadership to establish the operation of a GMP cell therapy manufacturing facility from scratch
- Hire & manage operational staff, including developing staff capabilities through initial and ongoing training and maintaining team compliance
- Provide management oversight of international tech transfer activities
- Manage the production schedule and the daily tasks of the Manufacturing Operators
- Provide oversight and guidance related to training materials, SOPs, batch records, reports, risk assessments, materials management, etc
- Work cross-functionally with process development, quality, and other counterparts for the development of next-generation cGMP cell therapy manufacturing processes
- Works closely with senior management to initiate new projects and assist in developing processes/techniques to meet business objectives
Basic Qualifications:
- Master’s degree in life science or engineering with a minimum of 5 years of industry experience.
- 2 years in managing direct reports or project teams
- 2 years of experience in cell therapy
- Experience in GMP documentation and compliance
- Ability to operate and thrive in a fast-paced, high-growth environment.
- Problem solving and can-do approach
- Excellent communication skills
Preferred Qualifications:
- MSc in cell biology or biotechnology
- Specific experience in cell GMP manufacturing facilities with expertise in cell therapy
- Involvement in delivering a cell therapy-based product into clinical development