Director Engineering Cell Therapy information
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$89.5K - $105.9K
5% of jobs
$105.9K - $122.4K
6% of jobs
$122.4K - $138.8K
9% of jobs
$140.1K is the 25th percentile. Wages below this are outliers.
$138.8K - $155.3K
11% of jobs
$155.3K - $171.7K
7% of jobs
$171.7K - $188.2K
7% of jobs
The median wage is $189.6K / yr.
$188.2K - $204.6K
6% of jobs
$204.6K - $221.1K
3% of jobs
$221.1K - $237.5K
1% of jobs
$243.7K is the 75th percentile. Wages above this are outliers.
$237.5K - $254K
40% of jobs
How much do director engineering cell therapy jobs pay per year?
As of Sep 14, 2026, the average yearly pay for director engineering cell therapy in the United States is $194,709.00, according to ZipRecruiter salary data. Most workers in this role earn between $141,500.00 and $253,000.00 per year, depending on experience, location, and employer.
A Director of Engineering in Cell Therapy oversees the development, optimization, and implementation of processes and technologies used in cell therapy manufacturing and research. They lead engineering teams, ensure regulatory compliance, and collaborate with scientists and other departments to scale up production while maintaining product quality and safety. Their role is critical in bringing innovative cell therapy treatments from the laboratory to clinical and commercial settings.
To thrive as a Director of Engineering in Cell Therapy, you need advanced knowledge of cell therapy manufacturing, leadership experience, and a degree in engineering, biotechnology, or a related field. Familiarity with GMP regulations, bioprocessing equipment, automation systems, and quality management certifications (such as Six Sigma or Lean) is often required. Strategic thinking, strong communication, and the ability to lead multidisciplinary teams are crucial soft skills for this role. These competencies ensure the safe, efficient, and compliant development of innovative cell-based therapies in a highly regulated environment.
A Director of Engineering in Cell Therapy often encounters challenges related to transitioning processes from small-scale laboratory settings to large-scale, compliant manufacturing environments. This includes ensuring product consistency, meeting strict regulatory requirements, and managing cross-functional teams to coordinate technology transfer. Additionally, keeping up with rapid advancements in cell therapy technologies and integrating automated systems while maintaining high quality standards can be demanding. Success in this role requires excellent project management skills and effective collaboration with R&D, quality assurance, and operations teams.
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