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Full Time Chimeric Therapeutics Jobs (NOW HIRING)

Legend Biotech USA, Inc.

... chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based ... Apply a strong understanding of therapeutic area, disease biology, and clinical endpoints to ...

Legend Biotech USA, Inc.

$83K - $109K/yr

... chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based ... edge therapeutics for patients worldwide.Legend Biotech entered into a global collaboration ...

Legend Biotech USA, Inc.

$146K - $192K/yr

... chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based ... edge therapeutics for patients worldwide.Legend Biotech entered into a global collaboration ...

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All JobsChimeric Therapeutics JobsFull Time Chimeric Therapeutics Jobs

Full Time Chimeric Therapeutics information

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$11K

$133.1K

$245K

How much do full time chimeric therapeutics jobs pay per year?

As of Jul 29, 2026, the average yearly pay for full time chimeric therapeutics in the United States is $133,142.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,000.00 and $228,000.00 per year, depending on experience, location, and employer.

What are some typical challenges faced by employees working full time at Chimeric Therapeutics, and how does the company support their professional development?

Employees at Chimeric Therapeutics often work in a fast-paced, innovative environment focused on advancing cell therapies. Common challenges include keeping up with rapidly evolving scientific research, navigating regulatory requirements, and collaborating across multidisciplinary teams. The company supports professional development by offering ongoing training, access to scientific conferences, and mentorship programs, helping team members stay current and grow within the organization. This collaborative culture fosters both individual and collective success, making it an ideal environment for those passionate about biotechnology and medical innovation.

What is the difference between Full Time Chimeric Therapeutics vs Full Time Cell Therapy Research Associate?

AspectFull Time Chimeric TherapeuticsFull Time Cell Therapy Research Associate
Required CredentialsBachelor's or Master's in biology, immunology, or related field; experience in cell engineeringBachelor's or Master's in biology, biomedical sciences; laboratory experience in cell culture
Work EnvironmentBiotech labs focused on gene editing and immunotherapy developmentResearch labs conducting cell culture, assays, and preclinical studies
Employer & Industry UsageBiotech companies specializing in immunotherapy and gene editingResearch institutions and biotech firms in cell therapy development

Full Time Chimeric Therapeutics roles focus on developing engineered immune cells for therapies, requiring specialized knowledge in gene editing. Full Time Cell Therapy Research Associates support laboratory research in cell culture and assays, with a broader focus on preclinical studies. Both roles are vital in the cell therapy industry but differ in technical focus and responsibilities.

What are the key skills and qualifications needed to thrive in a full-time role at Chimeric Therapeutics, and why are they important?

To excel in a full-time position at Chimeric Therapeutics, you typically need a strong background in biotechnology, life sciences, or a related field, often supported by relevant degrees or research experience. Familiarity with laboratory techniques, cell therapy platforms, and compliance with regulatory systems like GMP is essential. Strong analytical thinking, teamwork, and effective communication are valuable soft skills for this environment. These abilities ensure accurate research, successful project execution, and collaboration in the fast-paced field of cellular therapeutics.

What are Full Time positions at Chimeric Therapeutics?

Full Time positions at Chimeric Therapeutics refer to roles where employees work a standard number of hours, typically 38-40 hours per week, and are dedicated exclusively to the company's operations. These roles can include research scientists, project managers, clinical specialists, and administrative staff focused on developing and advancing cell therapies, particularly CAR-T therapies for cancer. Full Time staff often receive benefits such as health coverage, paid leave, and opportunities for career growth within the biotechnology sector. Working Full Time at Chimeric Therapeutics means being part of a team dedicated to innovative treatments and clinical advancements.
More about Full Time Chimeric Therapeutics jobs
What cities are hiring for Full Time Chimeric Therapeutics jobs? Cities with the most Full Time Chimeric Therapeutics job openings:
What are the most commonly searched types of Chimeric Therapeutics jobs? The most popular types of Chimeric Therapeutics jobs are:
What job categories do people searching Full Time Chimeric Therapeutics jobs look for? The top searched job categories for Full Time Chimeric Therapeutics jobs are:
Full Time Chimeric Therapeutics jobs near you
Infographic showing various Full Time Chimeric Therapeutics job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $133,142 per year, or $64 per hour.
Process & Analytical Development Specialist

Process & Analytical Development Specialist

Verismo Therapeutics

Philadelphia, PA

Full-time

Posted 20 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.

Apply