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Cell Therapy Process Development Jobs in Pennsylvania

Bristol Myers Squibb

... development of the area-level and account-specific plans. For this position the company seeks a ... Clearly communicate updates on CART processes to facility stakeholders to ensure their ...

Legend Biotech US

Scientist

Philadelphia, PA · On-site

... cell line optimization. * Perform media optimization, feeding strategy development, and process ... Experience supporting gene therapy platform development, preferably involving lentiviral vector ...

USWM, LLC

Associate Scientist - MSAT

Philadelphia, PA · On-site

$70K - $110K/yr

Experience in a biotechnology company with emphasis on immunological systems, cell therapy, gene therapy, and large-scale process development and improvement. * Experience in a cGMP or GLP ...

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Cell Therapy Process Development information

What are the key skills and qualifications needed to thrive as a cell therapy process development professional?

To thrive in Cell Therapy Process Development, you need a solid background in cell biology, biotechnology, or a related field, often supported by a relevant degree and experience with cell culture techniques. Familiarity with bioprocessing equipment, Good Manufacturing Practice (GMP) regulations, and analytical tools such as flow cytometry and PCR is typically required. Strong problem-solving skills, attention to detail, and effective teamwork enhance performance in this collaborative and innovative environment. These competencies ensure the safe and efficient development of cell therapies, meeting rigorous quality standards and advancing clinical applications.

What are some typical challenges faced by professionals in cell therapy process development, and how are they addressed?

Professionals in Cell Therapy Process Development often encounter challenges such as scaling up production processes from laboratory to clinical or commercial scale while maintaining product quality and consistency. Additional hurdles include adhering to strict regulatory requirements and managing complex collaborations across cross-functional teams, like quality assurance, regulatory affairs, and manufacturing. These challenges are typically addressed through rigorous process optimization, thorough documentation, and ongoing communication with stakeholders to ensure that all aspects of the process meet industry standards and regulatory expectations.

What is the difference between Cell Therapy Process Development vs Cell Therapy Manufacturing Specialist?

AspectCell Therapy Process DevelopmentCell Therapy Manufacturing Specialist
CredentialsTypically requires a degree in biology, biochemistry, or biomedical engineering; certifications in GMP or cell therapy are commonSimilar credentials; often holds degrees in related fields and GMP certifications
Work EnvironmentResearch labs, development facilities, early-stage process optimizationManufacturing plants, production floors, quality control labs
Industry UsageFocuses on developing and optimizing cell therapy processesInvolved in large-scale production and process execution

Cell Therapy Process Development professionals focus on designing and refining cell therapy procedures, while Cell Therapy Manufacturing Specialists handle the production and quality assurance in manufacturing settings. Both roles require similar educational backgrounds and certifications but differ mainly in their work environment and specific responsibilities.

What is cell therapy process development?

Cell Therapy Process Development refers to the design, optimization, and scaling up of manufacturing processes for cell-based therapies, such as CAR-T cells or stem cell products. Professionals in this field work on translating laboratory research into reproducible, efficient, and safe production methods that meet regulatory standards. This involves working with cell culture techniques, bioreactors, quality control, and process validation to ensure that therapies can be produced consistently for clinical and commercial use. The goal is to develop robust processes that deliver safe and effective cell therapies to patients.
What are popular job titles related to Cell Therapy Process Development jobs in Pennsylvania? For Cell Therapy Process Development jobs in Pennsylvania, the most frequently searched job titles are:
What job categories do people searching Cell Therapy Process Development jobs in Pennsylvania look for? The top searched job categories for Cell Therapy Process Development jobs in Pennsylvania are:
What cities in Pennsylvania are hiring for Cell Therapy Process Development jobs? Cities in Pennsylvania with the most Cell Therapy Process Development job openings:
Cell Therapy Process Development jobs near you
Infographic showing various Cell Therapy Process Development job openings in Pennsylvania as of August 2026, with employment types broken down into 68% Full Time, and 32% Part Time. Highlights an 100% In-person job distribution.

Process & Analytical Development Specialist

Verismo Therapeutics

Philadelphia, PA • On-site

Full-time

Re-posted 2 days ago

Job description

Process & Analytical Development Specialist 


Full-Time position
Level: Specialist
Location: On-site in Philadelphia PA
Start date: Open


Why Join Verismo?

Our team is small but driven, with the single focus of bringing life-changing cell therapies to patients with cancer. With a solid pipeline built around a novel KIR-CAR platform, our technology has found a way to circumvent the barriers in solid cancer where other CAR therapies have limited success. KIR-CARs eliminate the artificial chimeric constructs within T cells and instead use a natural NK-cell derived signaling system. This system is potent against both hematologic and solid tumors, and in preclinical models is superior to current CAR-T in conferring long-term sustained anti-tumor function to overcome the challenges posed in solid cancer. We have a strong team for CMC, clinical product manufacture, and clinical investigators already established and moving fast to bring KIR-CARs to patients in need.

Our company is comprised of individuals who each bring something unique to the table and are valued for their contributions. Our culture is based on the concept of 'love what you do' and the dedication that builds a team where people do their best and support one another. Because we believe our people are our greatest asset, career development is an important aspect of our investment in our team and we encourage work/life balance.

About the Position:

We are seeking a passionate and skilled Process & Analytical Development Specialist to join our growing CMC team. In this role, you will play a pivotal role in advancing Verismo's cell therapy products by supporting process and analytical development activities. Reporting directly to the Senior Manager of Process Development, you will contribute hands-on expertise to scale up processes, analyze data, and support tech transfers to external manufacturing partners.

Essential Duties & Responsibilities:
  • Contribute to the setup and organization of Verismo Therapeutics' process and analytical development capabilities.
  • Execute complex development studies (with multiple experiment sets) related to process development and scale-up, ensuring studies balance time and resources.
  • Apply Quality by Design (QBD) principals to process development, characterization, establish process parameters, and contribute to CMC regulatory filings.
  • Support next generation manufacturing processes and analytics for cell therapy and lentiviral vector
  • Author technical and scientific documents including but not limited to SOPs, Master Batch Records, study protocols and reports.
  • Ensure all documentation and reports are accurate, complete, and suitable for support of development, characterization, and regulatory approval of products.

Preferred Experience & Abilities:
  • Experience in a cGMP manufacturing and/or QC setting or process and/or analytical development laboratory
  • Background in cell processing, scale up and tech transfer
  • Working knowledge of analytical tools commonly utilized in cell therapy manufacturing
  • Familiarity with quality by design (QbD) approaches and design of experiment (DoE) based studies
  • Ability to function in a dynamic environment.
  • Knowledge of GMP regulations as it pertains to best practices in cGMP manufacturing
  • Experience with Good Documentation Practices (GDP)

Qualification Requirements:

Bachelor's degree in a scientific field with at least 2 years of relevant experience.

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