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Associate Director Stem Cell Therapy Jobs (NOW HIRING)

City of Hope

Registered Nurse, Stem Cell

Goodyear, AZ · On-site

Collaborates with physicians and other health care providers to provide direct and indirect care to ... Therapy experience (Stem Cell Transplant and/or Immune Effector Cell), CAR-T * Associate Degree in ...

City of Hope

Registered Nurse, Stem Cell

Goodyear, AZ · On-site

Collaborates with physicians and other health care providers to provide direct and indirect care to ... Therapy experience (Stem Cell Transplant and/or Immune Effector Cell), CAR-T * Associate Degree in ...

Novartis

$138K - $257K/yr

Summary #LI-Remote The Associate Director Cell Therapy Operations Manager is in the Southeast geography. This is a remote& field-based role that covers thefollowing, butnot limited to:Atlanta, GA ...

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Associate Director Stem Cell Therapy information

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$30.5K

$102.7K

$173K

How much do associate director stem cell therapy jobs pay per year?

As of Sep 11, 2026, the average yearly pay for associate director stem cell therapy in the United States is $102,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $141,000.00 per year, depending on experience, location, and employer.

What does an associate director in stem cell therapy do?

An Associate Director of Stem Cell Therapy oversees research, development, and implementation of stem cell-based treatments in clinical or laboratory settings. They are responsible for managing teams, guiding scientific strategy, ensuring regulatory compliance, and collaborating with other departments or external partners. Their role also involves monitoring project progress, securing funding, and staying updated with advances in stem cell science to drive innovation within their organization.

What are the key skills and qualifications needed to thrive as an associate director in stem cell therapy?

To thrive as an Associate Director in Stem Cell Therapy, you need advanced expertise in cell biology, regenerative medicine, and clinical research, typically supported by a PhD or MD and relevant industry experience. Familiarity with laboratory information management systems (LIMS), GMP/GLP compliance, and regulatory documentation is essential, along with certifications such as RAC (Regulatory Affairs Certification) being advantageous. Strong leadership, strategic thinking, and effective communication skills set outstanding candidates apart by enabling successful team management and cross-functional collaboration. These competencies are critical for driving innovative therapies, ensuring regulatory compliance, and leading multidisciplinary teams in a rapidly evolving field.

What are the main challenges an associate director in stem cell therapy might face when leading multidisciplinary teams?

As an Associate Director of Stem Cell Therapy, one significant challenge is effectively coordinating work between scientists, clinicians, regulatory experts, and manufacturing teams. Balancing innovative research with the strict regulatory and compliance requirements of cell therapy can be complex. Additionally, adapting to rapidly evolving scientific advancements while ensuring project timelines and budget goals are met requires strong leadership and communication skills. Successful candidates are able to foster collaboration across diverse teams and drive projects forward despite these challenges.

What is the difference between Associate Director Stem Cell Therapy vs Senior Research Scientist?

AspectAssociate Director Stem Cell TherapySenior Research Scientist
Required CredentialsAdvanced degree (PhD or MD), leadership experience, industry certificationsMaster's or PhD, specialized research experience
Work EnvironmentLeadership role in biotech or pharma companies, overseeing projectsLaboratory research, experimental design, data analysis
Employer & Industry UsageBiotech, regenerative medicine, pharmaceutical companiesResearch institutions, biotech firms, academia

The Associate Director Stem Cell Therapy typically holds a leadership position with strategic responsibilities, overseeing research teams and projects in biotech or pharma settings. In contrast, a Senior Research Scientist focuses on hands-on research and experimental work. Both roles require advanced degrees and specialized knowledge, but the Associate Director emphasizes management and strategic planning, while the Senior Research Scientist concentrates on scientific experimentation and data analysis.

What states have the most Associate Director Stem Cell Therapy jobs?

States with the most job openings for Associate Director Stem Cell Therapy jobs include:

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

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

Infographic showing various Associate Director Stem Cell Therapy job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 68% Full Time, 28% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $102,728 per year, or $49.4 per hour.

Associate Director, Process Development, Cell Therapy

Santa Monica, CA • On-site

AstraZeneca
Pharmaceutical Product Wholesalers • 10K+ employees
Learn more about AstraZenecaexternal

$138K - $207K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday

Key responsibilities

  • Lead the late-stage process development for cell therapies, managing multiple projects.

  • Guide scientists and engineers in delivering technical documentation, performing risk assessments, data analysis, and presenting study outcomes.

  • Support process transfer, lifecycle management activities, and manufacturing support including deviation management and regulatory documentation.

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

Job description

Position Summary
The Associate Director, Late-Stage Cell Therapy Process Development, will provide scientific and technical leadership for the development, characterization, and transfer of manufacturing processes for cell therapy products. This role is responsible for leading a team of scientists and engineers supporting process development activities from clinical development through commercialization, including BLA and global regulatory submissions. The successful candidate will partner cross-functionally with Manufacturing, Quality, Regulatory Affairs, Analytical Development, and CMC teams to ensure robust, compliant, and scalable manufacturing processes.
Key Responsibilities
Technical Leadership
  • Lead the late-stage process development for cell therapies within the Process Engineering function, managing multiple development projects

  • Direct and guide engineers/scientists to deliver high-quality technical documentation for the study design, laboratory execution and report authoring activities

  • Perform risk assessment, data analysis, write technical reports, and present outcome of the studies to cross-functional teams and governance forums

  • Conduct batch record review, deviation assessment, and data trending to ensure robustness of cell therapy manufacturing processes

  • Apply AI-enabled tools and digital analytics to accelerate data review, trend analysis, batch record evaluation, and process understanding

Team Leadership and Management
  • Build, develop, and manage a high-performing team of process development scientists and engineers

  • Establish project priorities, resource allocation, and departmental objectives

  • Foster a collaborative and innovation-driven culture

PPQ & Technology Transfer
  • Support PPQ activities including but not limited to protocol authoring, batch record authoring and planning

  • Support technology transfer of cell therapy processes to internal manufacturing sites including make-a-batch assessments and drafting manufacturing batch records

Lifecycle Management
  • Lead lifecycle management activities for commercial cell therapy products, including process monitoring, continuous improvement, post-approval changes, comparability assessments, and regulatory commitments.

  • Partner with Manufacturing, Quality, Regulatory Affairs, and Technical Operations to implement process improvements, maintain process control, and support ongoing commercial readiness.

Manufacturing Support & Scientific Deviation Management
  • Serve as the Process Development and Engineering SME for manufacturing operations, providing scientific support for deviations, investigations, atypical events, and process-related issues.

  • Lead root cause analyses, impact assessments, and CAPA development using data-driven and risk-based approaches to ensure product quality, compliance, and uninterrupted manufacturing operations.

Regulatory Support
  • Contributes to authoring and reviewing CMC documentation, including cell therapy process descriptions, characterization summaries, PPQ protocols and reports, and control strategy elements.

  • Support preparation of BLA/MAA submissions and responses to regulatory questions related to cell therapy manufacturing.

Cross-Functional Collaboration
  • Work closely with analytical sciences, quality, regulatory, and manufacturing teams to ensure end-to-end process alignment.

  • Represent cell therapy characterization activities in technical meetings, reviews, and governance discussions.

Required Qualifications
  • Ph.D. in Chemical Engineering, Biochemical Engineering, Biological Sciences, Biotechnology, Pharmaceutical Sciences, or related discipline with 6+ years of industry experience; or M.S. with 10+ years of relevant experience; or B.S. with 12+ years of relevant experience.

  • Strong technical expertise in cell therapy process development, GMP operations and late-stage / commercial readiness.

  • Experience with late-stage development, and PPQ for cell therapy processes.

  • Demonstrated proficiency in applying AI tools and digital solutions to data analysis, documentation, and workflow automation.

  • Strong technical writing, data analysis, and problem-solving skills.

Preferred Qualifications
  • Experience with commercial-stage cell therapy or biologics products.

  • Experience supporting PPQ, process validation, and post-approval changes.

  • Familiarity with global regulatory requirements and lifecycle management strategies.

  • Experience designing and executing DOE and multivariate data analysis for cell therapy processes.

Key Competencies
  • Strong team management and talent development experience

  • Excellent cross-functional communication and collaboration.

  • Ability to operate effectively in fast-paced, late-stage development environments.

  • Scientific curiosity, ownership mindset, and willingness to support manufacturing operations.

The annual base pay for this position ranges from $138K to $207K. Our positions offer eligibility for multiple incentives an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
# Hybrid # Cell Therapy
Date Posted
01-Sep-2026
Closing Date
13-Sep-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB

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