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Director Engineering Cell Therapy Jobs (NOW HIRING)

Autolus Therapeutics PLC

Using a broad suite of proprietary and modular T cell programming technologies, the company is ... The Director, Payer Access Cell Therapy will be an integral member of the commercial organization ...

Autolus Therapeutics plc

Director, Payer Access Cell Therapy (PACT) Reports to: VP US Head of Market Access Department ... Using a broad suite of proprietary and modular T cell programming technologies, the company is ...

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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:

Associate Director, T Cell Engineering & Translation

Manhattan, NY • On-site

Weill Cornell Medical College
Health Care and Social Assistance • 501 - 1,000 employees
Learn more about Weill Cornell Medical Collegeexternal

$203K - $236K/yr

Full-time

Posted 5 days ago

Weill Cornell Medicine rating

7.5

Company rating: 7.5 out of 10

Based on 64 frontline employees who took The Breakroom Quiz

Job description

Title: Associate Director, T Cell Engineering & Translation
Location: Upper East Side
Org Unit: MCC Laboratories
Work Days:
Weekly Hours: 35.00
Exemption Status: Exempt
Salary Range: $203,700.00 - $236,500.00
*As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices
Position Summary
Responsible for leading the engineering, process development, and translational advancement of TCR engineered T cell therapies from candidate nomination through clinical readiness. The Associate Director drives vector design, cell engineering, and preclinical development of next-generation TCR-T cell therapies and provides cross-functional scientific leadership across research, manufacturing, quality, and clinical translation activities.
Job Responsibilities
  • Develop effective vivo T cell engineering strategies and delivery vectors.
  • Lead optimization of viral and non-viral vector designs for in vivo and ex vivo generation of armored TCR-T cells.
  • Provide scientific leadership for translational development activities supporting clinical readiness and IND-enabling programs.
  • Collaborate with Vector Production, Quality, and Manufacturing leadership to transition preclinical products into scalable clinical processes.
  • Evaluate TCR constructs for stability, reactivity, safety, and manufacturability.
  • Oversee development and optimization of ex vivo TCR-T manufacturing processes.
  • Conduct and direct IND-enabling studies integrating pharmacology, safety, potency, and mechanism-of-action data.
  • Serve as the scientific liaison between discovery, translational, and manufacturing teams.
  • Drive process improvements and strategic enhancements in cell therapy manufacturing and development.
  • Ensure documentation standards support future regulatory submissions and clinical translation

Education
  • Master's Degree or Ph.D. in an appropriate field. Equivalent work experience will be considered.

Experience
  • 10+ years in T cell engineering, cell therapy, or gene therapy development.
  • Approximately 3+ years of experience leading translational or IND-enabling development programs in academic, biotechnology, or pharmaceutical settings.
  • Demonstrated cross-functional leadership of scientific teams and complex development initiatives.

Knowledge, Skills and Abilities
  • Expert knowledge of TCR-T cell biology, receptor engineering, and gene modification platforms.
  • Knowledge of vector design, optimization, and safety-switch technologies.
  • Understanding of translational development pathways from preclinical research through early-phase clinical trials.
  • Knowledge of regulatory expectations and compliance standards supporting clinical translation.
  • Ability to provide strategic scientific leadership across multidisciplinary teams.

Licenses and Certifications
Working Conditions/Physical Demands
Ability to work flexible hours, evenings and weekends, when requested for special projects.
Cornell welcomes students, faculty, and staff with diverse backgrounds from across the globe to pursue world-class education and career opportunities, to further the founding principle of "any person, any study." No person shall be denied employment on the basis of any legally protected status or subjected to prohibited discrimination involving, but not limited to, such factors as race, ethnic or national origin, citizenship and immigration status, color, sex, pregnancy or pregnancy-related conditions, age, creed, religion, actual or perceived disability (including persons associated with such a person), arrest and/or conviction record, military or veteran status, sexual orientation, gender expression and/or identity, an individual's genetic information, domestic violence victim status, familial status, marital status, or any other characteristic protected by applicable federal, state, or local law.
Cornell University embraces diversity in its workforce and seeks job candidates who will contribute to a climate that supports students, faculty, and staff of all identities and backgrounds. We hire based on merit, and encourage people from historically underrepresented and/or marginalized identities to apply. Consistent with federal law, Cornell engages in affirmative action in employment for qualified protected veterans as defined in the Vietnam Era Veterans' Readjustment Assistance Act (VEVRRA) and qualified individuals with disabilities under Section 503 of the Rehabilitation Act. We also recognize a lawful preference in employment practices for Native Americans living on or near Indian reservations in accordance with applicable law.

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