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Director Cell Therapy Jobs (NOW HIRING)

... cell therapies. The Marketplace Director operates with an ownership mindset, leads through influence in a matrix environment, and ensures teams are enabled, aligned, and accountable to deliver ...

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Director Cell Therapy information

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$23K

$136.1K

$237.5K

How much do director cell therapy jobs pay per year?

As of Jul 14, 2026, the average yearly pay for director cell therapy in the United States is $136,062.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,500.00 and $181,000.00 per year, depending on experience, location, and employer.

What are Director Cell Therapy roles?

A Director of Cell Therapy is a senior leader responsible for overseeing the development, manufacturing, and clinical application of cell-based therapies, such as CAR-T treatments. They manage teams involved in research, production, quality assurance, and regulatory compliance. This role often involves strategic planning, cross-functional collaboration, and ensuring that therapies meet safety and efficacy standards required for regulatory approvals. Directors may also engage with external partners, stakeholders, and regulatory agencies to advance cell therapy programs from research to commercialization.

What are some common challenges faced by a Director of Cell Therapy when leading cross-functional teams?

A Director of Cell Therapy often manages teams that span research, clinical development, manufacturing, and regulatory affairs. Coordinating communication and aligning objectives across these diverse groups can be challenging, as each team may have different priorities and technical languages. Additionally, the rapid pace of innovation in cell therapy requires the Director to stay current with scientific advances while ensuring compliance with evolving regulations. Successful Directors foster collaboration, provide clear direction, and proactively address potential bottlenecks to keep projects on track.

What are the key skills and qualifications needed to thrive as a Director of Cell Therapy, and why are they important?

To thrive as a Director of Cell Therapy, you need advanced expertise in cellular and molecular biology, clinical research, and regulatory compliance, often supported by a PhD or MD and extensive industry experience. Familiarity with cell processing technologies, GMP manufacturing, and regulatory submission systems is critical. Leadership, strategic vision, and strong communication skills help drive cross-functional teams and collaborations. These skills ensure effective program oversight, regulatory success, and innovation in cell therapy development.
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What states have the most Director Cell Therapy jobs? States with the most job openings for Director Cell Therapy jobs include:
Infographic showing various Director Cell Therapy job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 71% Full Time, 27% Part Time, and 1% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $136,062 per year, or $65.4 per hour.

Director/Associate Director, Cell Therapy CMC & Manufacturing

QLD Biotherapeutics Inc

Boston, MA โ€ข On-site

Full-time

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Director/Associate Director, Cell Therapy CMC & Manufacturing

We are seeking a highly experienced and visionary leader of CMC & Manufacturing to lead our cell therapy development programs. The successful candidate will help lead CMC strategy, manage process development and manufacturing activities, and play a key role in advancing programs into first-in-human clinical trials. This role requires demonstrated success in bringing at least one cell therapy program from preclinical through IND and into clinical trials.

Key Responsibilities

  • Lead/support the development and implementation of CMC strategy for cell therapy programs.
  • Lead process development and optimization for iPSC- or MSC-derived products and drive process development, scale-up, and tech transfer.
  • Contribute to regulatory filings (CMC sections of IND/CTA).
  • Collaborate with CMC, R&D, QC, QA, and clinical teams across China and the U.S. to ensure a seamless transition from preclinical to clinical development.
  • Support resource planning, budgeting, and project management for CMC deliverables.
  • Provide strategic leadership to ensure clinical readiness and robust supply chain for first-in-human studies.

Qualifications

  • PhD (preferred) or MS in Cell Biology, Immunology, Bioengineering, or related field.
  • 8+ years of biotech/pharma experience with at least 5 years in cell therapy CMC leadership.
  • Hands-on experience with iPSC/MSC biology, process development, and GMP compliance.
  • Proven track record of advancing programs into IND/clinical development.
  • Deep knowledge of GMP regulations, regulatory expectations, and cell therapy manufacturing platforms.
  • Excellent leadership, communication, and cross-functional team management skills.
  • Strong interpersonal and communication skills; ability to thrive in a fast-paced, collaborative biotech environment.
  • Strong leadership, project management, and cross-functional communication skills.

We are an equal opportunities employer and welcome applications from all qualified candidates.

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