Home › Companies › Aa067 Sci Rsrch En › Director of Cellular Immunotherapy GMP Manufacturing
Director of Cellular Immunotherapy GMP Manufacturing
Aa067 Sci Rsrch En · United States-California-Duarte · Active · Oracle Taleo Enterprise
Job facts
| Field | Value |
|---|---|
| Company | Aa067 Sci Rsrch En |
| Title | Director of Cellular Immunotherapy GMP Manufacturing |
| Normalized title | - |
| Department / team | Days |
| Location | Duarte, CA, United States |
| Work model | - |
| Employment type | - |
| Salary | - |
| Status | active |
| ATS provider | Oracle Taleo Enterprise |
| Posted / first seen | — / 2026-05-31 |
| Changed / last seen | 2026-06-05 / 2026-06-06 |
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| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Duarte. | Open |
| Department jobs | Active postings in Days. | Open |
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| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Aa067 Sci Rsrch En |
| Source | f78e7b35-939f-4bec-9d27-0fe8f2343d0b |
| ATS provider | Oracle Taleo Enterprise |
Description
Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.
We are looking for a leader to head the Manufacturing of Cellular Immunotherapies in Cell and Gene Therapy Operations. This role reports to the Vice President of Cell and Gene Therapy Operations / Director of the Center for Bioinnovation and Manufacturing.
COH has a mission to transform the future of cancer care. In support of this mission, COH has over 20+ years of experience in GMP production of Cell and Gene Therapies holding >120 active INDs and supported by an 80+ person GMP team. The new Director will oversee a Manufacturing team of >15 people that focuses primarily on autologous production of >60 CAR-T therapies per year in support of early clinical trials. Additional relevant areas of expertise are manufacturing of TILs and CAR-NK.
As a successful candidate you will:
· Lead and manage a high-performing team responsible for cGMP manufacturing of cellular immunotherapy products.
· Ensure execution of manufacturing processes that meet rigorous safety, quality, and compliance standards.
· Oversee GMP manufacturing logistics, including scheduling, resource allocation, and throughput optimization.
· Troubleshoot and resolve issues, identify root causes, and implement process improvements with clear communication to senior leadership and project PIs.
· Develop and monitor KPIs for productivity, efficiency, and compliance.
· Drive continuous improvement initiatives, leveraging advanced technologies and best practices.
· Ensure adequate staffing, facilities, equipment, and documentation to meet evolving priorities and capacity needs.
· Collaborate with internal stakeholders to align manufacturing operations with institutional goals.
· Partner with Project Management to develop budgets for internal and external projects.
· Recruit, train, and mentor team members, fostering professional growth and career development.
· Establish organizational structure, policies, and production schedules to support operational excellence.
· Promote a culture of collaboration, accountability, and innovation
Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.
We are looking for a leader to head the Manufacturing of Cellular Immunotherapies in Cell and Gene Therapy Operations. This role reports to the Vice President of Cell and Gene Therapy Operations / Director of the Center for Bioinnovation and Manufacturing.
COH has a mission to transform the future of cancer care. In support of this mission, COH has over 20+ years of experience in GMP production of Cell and Gene Therapies holding >120 active INDs and supported by an 80+ person GMP team. The new Director will oversee a Manufacturing team of >15 people that focuses primarily on autologous production of >60 CAR-T therapies per year in support of early clinical trials. Additional relevant areas of expertise are manufacturing of TILs and CAR-NK.
As a successful candidate you will:
· Lead and manage a high-performing team responsible for cGMP manufacturing of cellular immunotherapy products.
· Ensure execution of manufacturing processes that meet rigorous safety, quality, and compliance standards.
· Oversee GMP manufacturing logistics, including scheduling, resource allocation, and throughput optimization.
· Troubleshoot and resolve issues, identify root causes, and implement process improvements with clear communication to senior leadership and project PIs.
· Develop and monitor KPIs for productivity, efficiency, and compliance.
· Drive continuous improvement initiatives, leveraging advanced technologies and best practices.
· Ensure adequate staffing, facilities, equipment, and documentation to meet evolving priorities and capacity needs.
· Collaborate with internal stakeholders to align manufacturing operations with institutional goals.
· Partner with Project Management to develop budgets for internal and external projects.
· Recruit, train, and mentor team members, fostering professional growth and career development.
· Establish organizational structure, policies, and production schedules to support operational excellence.
· Promote a culture of collaboration, accountability, and innovation
Your qualifications should include:
· Bachelor’s degree in biological sciences, engineering, or related field (Masters or PhD preferred).
· Minimum of 5 years of experience working with human T-cells, primary human cells, immune systems or similar biological systems.
· Minimum of 2 years of experience in cGMP cell therapy and/or biological product manufacturing, ideally with immunoeffector cell therapy focus.
· Minimum of 2 years supervisory experience and leading teams of greater than 5 people in a highly matrixed and milestone-driven environment.
· Strong understanding of CAR-T biology, including T-cell activation, cytotoxicity, and exhaustion.
· Strong Interpersonal and collaboration skills to interface with external groups.
· In-depth knowledge of cGMP regulations and FDA guidance for biologics and cell therapy.
· Experience in regulatory documentation (e.g., FDA CMC submissions).
City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.
City of Hope is an equal opportunity employer.
To learn more about our Comprehensive Benefits, please CLICK HERE .
Your qualifications should include:
· Bachelor’s degree in biological sciences, engineering, or related field (Masters or PhD preferred).
· Minimum of 5 years of experience working with human T-cells, primary human cells, immune systems or similar biological systems.
· Minimum of 2 years of experience in cGMP cell therapy and/or biological product manufacturing, ideally with immunoeffector cell therapy focus.
· Minimum of 2 years supervisory experience and leading teams of greater than 5 people in a highly matrixed and milestone-driven environment.
· Strong understanding of CAR-T biology, including T-cell activation, cytotoxicity, and exhaustion.
· Strong Interpersonal and collaboration skills to interface with external groups.
· In-depth knowledge of cGMP regulations and FDA guidance for biologics and cell therapy.
· Experience in regulatory documentation (e.g., FDA CMC submissions).
City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.
City of Hope is an equal opportunity employer.
To learn more about our Comprehensive Benefits, please CLICK HERE .
Full job record
| Job ID | b26087291079f754608a9373d8e2610e6a23f8fc |
| Org ID | 23a7cd11-5129-4d0d-8086-8a34956f4b37 |
| Source ID | f78e7b35-939f-4bec-9d27-0fe8f2343d0b |
| Board ID | f78e7b35-939f-4bec-9d27-0fe8f2343d0b |
| Provider | oracle_taleo |
| Provider Job Key | 224385 |
| Title | Director of Cellular Immunotherapy GMP Manufacturing |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | United States-California-Duarte |
| Department | Days |
| Team | — |
| Employment Type | — |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | CA |
| City | Duarte |
| Salary Raw | Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. We are looking for a leader to head the Manufacturing of Cellular Immunotherapies in Cell and Gene Therapy Operations. This role reports to the Vice President of Cell and Gene Therapy Operations / Director of the Center for Bioinnovation and Manufacturing. COH has a mission to transform the future of cancer care. In support of this mission, COH has over 20+ years of experience in GMP production of Cell and Gene Therapies holding >120 active INDs and supported by an 80+ person GMP team. The new Director will oversee a Manufacturing team of >15 people that focuses primarily on autologous production of >60 CAR-T therapies per year in support of early clinical trials. Additional relevant areas of expertise are manufacturing of TILs and CAR-NK. As a successful candidate you will: · Lead and manage a high-performing team responsible for cGMP manufacturing of cellular immunotherapy products. · Ensure execution of manufacturing processes that meet rigorous safety, quality, and compliance standards. · Oversee GMP manufacturing logistics, including scheduling, resource allocation, and throughput optimization. · Troubleshoot and resolve issues, identify root causes, and implement process improvements with clear communication to senior leadership and project PIs. · Develop and monitor KPIs for productivity, efficiency, and compliance. · Drive continuous improvement initiatives, leveraging advanced technologies and best practices. · Ensure adequate staffing, facilities, equipment, and documentation to meet evolving priorities and capacity needs. · Collaborate with internal stakeholders to align manufacturing operations with institutional goals. · Partner with Project Management to develop budgets for internal and external projects. · Recruit, train, and mentor team members, fostering professional growth and career development. · Establish organizational structure, policies, and production schedules to support operational excellence. · Promote a culture of collaboration, accountability, and innovation Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. We are looking for a leader to head the Manufacturing of Cellular Immunotherapies in Cell and Gene Therapy Operations. This role reports to the Vice President of Cell and Gene Therapy Operations / Director of the Center for Bioinnovation and Manufacturing. COH has a mission to transform the future of cancer care. In support of this mission, COH has over 20+ years of experience in GMP production of Cell and Gene Therapies holding >120 active INDs and supported by an 80+ person GMP team. The new Director will oversee a Manufacturing team of >15 people that focuses primarily on autologous production of >60 CAR-T therapies per year in support of early clinical trials. Additional relevant areas of expertise are manufacturing of TILs and CAR-NK. As a successful candidate you will: · Lead and manage a high-performing team responsible for cGMP manufacturing of cellular immunotherapy products. · Ensure execution of manufacturing processes that meet rigorous safety, quality, and compliance standards. · Oversee GMP manufacturing logistics, including scheduling, resource allocation, and throughput optimization. · Troubleshoot and resolve issues, identify root causes, and implement process improvements with clear communication to senior leadership and project PIs. · Develop and monitor KPIs for productivity, efficiency, and compliance. · Drive continuous improvement initiatives, leveraging advanced technologies and best practices. · Ensure adequate staffing, facilities, equipment, and documentation to meet evolving priorities and capacity needs. · Collaborate with internal stakeholders to align manufacturing operations with institutional goals. · Partner with Project Management to develop budgets for internal and external projects. · Recruit, train, and mentor team members, fostering professional growth and career development. · Establish organizational structure, policies, and production schedules to support operational excellence. · Promote a culture of collaboration, accountability, and innovation Your qualifications should include: · Bachelor’s degree in biological sciences, engineering, or related field (Masters or PhD preferred). · Minimum of 5 years of experience working with human T-cells, primary human cells, immune systems or similar biological systems. · Minimum of 2 years of experience in cGMP cell therapy and/or biological product manufacturing, ideally with immunoeffector cell therapy focus. · Minimum of 2 years supervisory experience and leading teams of greater than 5 people in a highly matrixed and milestone-driven environment. · Strong understanding of CAR-T biology, including T-cell activation, cytotoxicity, and exhaustion. · Strong Interpersonal and collaboration skills to interface with external groups. · In-depth knowledge of cGMP regulations and FDA guidance for biologics and cell therapy. · Experience in regulatory documentation (e.g., FDA CMC submissions). City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . Your qualifications should include: · Bachelor’s degree in biological sciences, engineering, or related field (Masters or PhD preferred). · Minimum of 5 years of experience working with human T-cells, primary human cells, immune systems or similar biological systems. · Minimum of 2 years of experience in cGMP cell therapy and/or biological product manufacturing, ideally with immunoeffector cell therapy focus. · Minimum of 2 years supervisory experience and leading teams of greater than 5 people in a highly matrixed and milestone-driven environment. · Strong understanding of CAR-T biology, including T-cell activation, cytotoxicity, and exhaustion. · Strong Interpersonal and collaboration skills to interface with external groups. · In-depth knowledge of cGMP regulations and FDA guidance for biologics and cell therapy. · Experience in regulatory documentation (e.g., FDA CMC submissions). City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://aa067.taleo.net/careersection/sci_rsrch/jobdetail.ftl?job=224385&lang=en |
| Apply URL | https://aa067.taleo.net/careersection/sci_rsrch/jobdetail.ftl?job=224385&lang=en |
| First Seen At | 2026-05-31 18:23:37Z |
| Last Seen At | 2026-06-06 13:45:28Z |
| Last Checked At | 2026-06-06 13:45:28Z |
| Last Changed At | 2026-06-05 03:57:05Z |
| Inactive At | — |
| Source Posted At | — |
| Source Updated At | — |
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