When it comes to connecting Forge with Ajinomoto’s global initiatives, Masahito Kuroda (Masa) plays a vital role in building bridges that drive innovation. As part of Forge's Client Development team, Masa helps identify new opportunities in Japan’s gene therapy space helping to bring global collaboration to life. Outside of work, you’ll often find Masa exploring the Columbus Zoo with his family, reminiscing about his tropical fish tanks back in Japan, or getting lost in a sci-fi novel like The Three-Body Problem. Learn more about Masa here ➡️ https://hubs.li/Q03PR-mY0
Forge Biologics
Biotechnology Research
Columbus, Ohio 29,242 followers
A member of Ajinomoto Bio-Pharma Services
About us
Forge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table, helping champion teams that are navigating the long road from the lab bench to the bedside. With a patients-first approach, we are forging new models for working together to better accelerate these transformative medicines to reach those who need them most.
- Website
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http://www.forgebiologics.com
External link for Forge Biologics
- Industry
- Biotechnology Research
- Company size
- 201-500 employees
- Headquarters
- Columbus, Ohio
- Type
- Privately Held
- Founded
- 2020
- Specialties
- AAV, Gene Therapy, Biotech, and cGMP
Locations
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Primary
Get directions
Columbus, Ohio, US
Employees at Forge Biologics
Updates
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Our featured AAV case study demonstrates how early assay design turned initial production runs into powerful learning tools. Early developers often ask, “How do I define QTPP and CQAs when I have so little insight into my product or process?” The answer starts with a preliminary QTPP that outlines the intended characteristics of the therapeutic, paired with early CQA targets to guide assay design. By testing early batches with a focused panel of assays, including a phase-appropriate potency assay, teams can begin linking process parameters to potency and consistency, refining CQAs with real data and building a foundation for process control and cGMP readiness. Explore more in our article: Where do I start and will it work? ➡️ https://hubs.li/Q03PJFtc0
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Making more—and testing it better. Forge performs 30+ in-house assays, from rcAAV to mass spectrometry, to enable efficient and accelerated characterization and release. Learn more: https://hubs.li/Q03Pt7xJ0
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Press play on discovery and stay curious! Subscribe to Forge on YouTube for lab life, 23 Questions, and more ➡️ https://hubs.li/Q03PkVyq0
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🔬 Hiring Spotlight: Senior Associate Scientist, Downstream Process Development Are you ready to play a hands-on role in advancing gene therapy manufacturing? We are seeking a Senior Associate Scientist to help develop and refine the downstream processes at Forge. In this role, you’ll be deeply involved in vector purification and process optimization, from culturing and transfection to harvest, lysis, and purification using techniques like FPLC and density gradients. You’ll also help maintain critical equipment and materials, ensuring our labs operate at the highest standards of quality and compliance. Your contributions will directly impact our mission of enabling access to life-changing gene therapies. Learn more & apply here ➡️ https://bit.ly/4nUVilZ
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Step inside our QC lab with Allison Creech as she calibrates the osmometer, a critical tool that helps us verify the safety and quality of every AAV product, all under one roof! #GLRWM #QualityInAction
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We know how important early molecular design decisions are for long-term manufacturing success. That’s why our team created this AAV developer checklist for GOI and rep/cap plasmids. It's a simple tool you can use right away to reduce risk and keep manufacturability in focus. Download your copy: https://bit.ly/496Krk9
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As one of only 30 CDMOs in the room, Forge joined discussions on how the FDA and industry can engage earlier to enable more efficient U.S. manufacturing of biological products. Christopher Shilling and our regulatory team break down important takeaways for AAV developers: a shift from inspection to partnership, decoupling facility readiness from product review timelines, establishing clearer mechanisms for early FDA engagement, and more. 🔗 Read here: https://bit.ly/4q5Zb96
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In honor of Breast Cancer Awareness Month, we were grateful to welcome guests from the Susan G. Komen Foundation to speak with She Forges, our women’s employee resource group. Their stories and insights inspired meaningful conversation around early detection, prevention, and the power of community support in the fight against breast cancer.
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We were honored to welcome Ajinomoto Co., Inc., CEO Shigeo Nakamura to Forge. His visit reflected the deep connection between Forge and Ajinomoto, grounded in a shared purpose to advance health and well-being through innovation. During the Town Hall, Mr. Nakamura shared his journey with Ajinomoto and spoke about how Forge’s work contributes to the Group’s broader mission of contributing to the well-being of all human beings, our society, and our planet. We’re grateful to Mr. Nakamura and Ajinomoto for their continued partnership and vision. Together, we’re strengthening our ability to enable access to life-changing gene therapies and make a lasting impact on global health.
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