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Director Engineering Cell Therapy Jobs (NOW HIRING)

The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is ...

New

... engineering of logic-gated CAR T/eTCR T cell circuits, gene delivery, genetic construct ... Experience mentoring and managing direct reports, including providing scientific and career ...

The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is ...

The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is ...

Biologist

Boston, MA · On-site

$48.69 - $57.28/hr

Design and engineer novel cell lines in iPSCs, tumor cell lines, and other immortalized and primary cell types to support allogeneic cell therapy programs * Generate stable engineered cell lines ...

Biologist

Boston, MA · On-site

$48.69 - $57.28/hr

Design and engineer novel cell lines in iPSCs, tumor cell lines, and other immortalized and primary cell types to support allogeneic cell therapy programs * Generate stable engineered cell lines ...

Biologist

Boston, MA · On-site

$48.69 - $57.28/hr

Design and engineer novel cell lines in iPSCs, tumor cell lines, and other immortalized and primary cell types to support allogeneic cell therapy programs * Generate stable engineered cell lines ...

Biologist

Boston, MA · On-site

$48.69 - $57.28/hr

Design and engineer novel cell lines in iPSCs, tumor cell lines, and other immortalized and primary cell types to support allogeneic cell therapy programs * Generate stable engineered cell lines ...

Biologist

Boston, MA · On-site

$48.69 - $57.28/hr

Design and engineer novel cell lines in iPSCs, tumor cell lines, and other immortalized and primary cell types to support allogeneic cell therapy programs * Generate stable engineered cell lines ...

Biologist

Boston, MA · On-site

$48.69 - $57.28/hr

Design and engineer novel cell lines in iPSCs, tumor cell lines, and other immortalized and primary cell types to support allogeneic cell therapy programs * Generate stable engineered cell lines ...

Biologist

Boston, MA · On-site

$48.69 - $57.28/hr

Design and engineer novel cell lines in iPSCs, tumor cell lines, and other immortalized and primary cell types to support allogeneic cell therapy programs * Generate stable engineered cell lines ...

Biologist

Boston, MA · On-site

$48.69 - $57.28/hr

Design and engineer novel cell lines in iPSCs, tumor cell lines, and other immortalized and primary cell types to support allogeneic cell therapy programs * Generate stable engineered cell lines ...

Showing results 21-40

Director Engineering Cell Therapy information

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$73K

$194.7K

$254K

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.

What does a director engineering cell therapy do?

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.

What are the key skills and qualifications needed to thrive as a director engineering cell therapy?

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.

What are the main challenges a director engineering cell therapy typically faces when scaling up manufacturing processes?

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.

What are popular job titles related to Director Engineering Cell Therapy jobs?

For Director Engineering Cell Therapy jobs, the most frequently searched job titles are:

Technical Operations Manager, GMP Engineering and Cell Manufacturing Facility

Buffalo, NY • On-site

Roswell Park Comprehensive Cancer Center
Hospitals • 1 - 5K employees

$111K - $135K/yr

Full-time

Posted 22 days ago


Roswell Park Comprehensive Cancer Center rating

8.1

Company rating: 8.1 out of 10

Based on 18 frontline employees who took The Breakroom Quiz


Job description

Title:
Technical Operations Manager, GMP Engineering and Cell Manufacturing Facility
Job Type:
RegularCompany:
Health Research, Inc. (HRI) Roswell Park DivisionDepartment:
Center for ImmunotherapyTime Type:
Full timeWeekly Hours:
40
FTE:
1Shift:
First Shift (United States of America)
Summary:
Leads a team of professional associates responsible for the manufacturing of CAR-T and other cell therapies within the GMP Engineering & Cell Manufacturing Facility. Oversees the day-to-day operations of cell therapy programs, including manufacturing and facilities cleaning and maintenance. Coordinates process and analytical development activities, ensuring compliance with cGMP (Good Manufacturing Practice) regulatory standards and safety protocols as well as managing the company's resources effectively. Ensures efficient production processes and effective analytical strategies and methods, coordinating with different departments, and implementing innovative approaches to improve productivity and profitability. Works closely with the team to provide process, material, and equipment knowledge to meet customer requirements and addresses operational and routine challenges as they arise for manufacturing. Participates and assists Technical Operations management with the preparation of budgets, statements of work, and other documents requested by internal and external customers required for reporting purposes, oversight of operations and for publication. The salary range for this position is $111,387 - $135,829 annually which includes a comprehensive benefits package. The actual offer may vary based on qualifications, skills, and experience.
Qualifications:
Required Education and Experience
1. PhD in a health, life science, engineering, or related field and the equivalent of five (5) years of full-time experience in GMP cell therapy, viral vector, gene therapy, biologics, or related advanced therapy manufacturing, process development, analytical development, quality control, or MSAT, including the equivalent of eighteen (18) months of experience in a supervisory, consultative, managerial, or executive capacity; or
2. Master's degree in a health, life science, engineering, or related field and the equivalent of seven (7) years of full-time experience in GMP cell therapy, viral vector, gene therapy, biologics, or related advanced therapy manufacturing, process development, analytical development, quality control, or MSAT, including the equivalent of eighteen (18) months of experience in a supervisory, consultative, managerial, or executive capacity; or
3. Bachelor's degree in a health, life science, engineering, or related field and the equivalent of nine (9) years of full-time experience in GMP cell therapy, viral vector, gene therapy, biologics, or related advanced therapy manufacturing, process development, analytical development, quality control, or MSAT, including the equivalent of eighteen (18) months of experience in a supervisory, consultative, managerial, or executive capacity.
NOTE:
Degrees must be conferred by an accredited school, college, or university, or by an institution recognized by Roswell Park Comprehensive Cancer Center and/or Health Research Incorporated as adhering to acceptable educational standards
Preferred Qualifications:
The preferred candidate will have:
Certified Scrum Master / Agile delivery experience (helpful for systems implementations and cross-functional execution)
Lean Six Sigma Black Belt (or equivalent demonstrated CI leadership)
CDMO experience, including client-facing delivery, tech transfer, and rapid timeline execution
Experience with common quality/systems tools (e.g., TrackWise / MasterControl / similar)
Equal Employment Opportunity Statement
Roswell Park Cancer Institute Corporation (RPCIC) and Health Research Inc. (HRI) Roswell Park Division believe that all persons are entitled to equal employment opportunities, and we do not discriminate against our employees, applicants or job seekers because of their race, color, religion, sex, sexual orientation, gender identity or expression, national origin, creed, age, disability, pregnancy-related condition, military or veteran status, marital or familial status, domestic violence victim status, citizenship status, genetic information, individual's relationship or association with a member of a protected category or any other protected group status as defined by law.
Affirmative Action/Equal Opportunity Employer/Qualified Individuals with Disabilities/Qualified Protected Veterans
Reasonable Accommodation Request
RPCIC and HRI are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email HR-BenefitsandLeaves@roswellpark.org and let us know the nature of your request and your contact information.
Our Core Values
RPCIC and HRI are committed to providing an environment where patients, families, employees and community are treated with courtesy and respect. We support an inclusive environment that nurtures the talents, skills and abilities of each individual to embody and reflect our core values: Innovation, Integrity, Teamwork, Commitment, Compassion and Respect.
Grant Funding
This is a grant-funded position. Compliance with funding requirements such as time and effort reporting, grant deliverables, and contract deliverables is required.
E-Verify Employer
Health Research Inc. (HRI) Roswell Park Division participates in the E-Verify program.

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