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Technician I, GMP Manufacturing - Downstream at Forge Biologics - ApplyBlast

Technician I, GMP Manufacturing - Downstream

Forge Biologics

1 month ago

4.1 on Glassdoor

Columbus, Ohio, United States

Onsite

Full Time

Junior

0 applicants

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About this role

The Technician I, GMP Manufacturing - Downstream plays a vital role in the production and purification of AAV-based gene therapy products in compliance with cGMP regulations. This position involves performing routine downstream manufacturing operations, operating specialized equipment, and executing purification processes to support the development of cutting-edge therapies. The role requires collaboration with cross-functional teams and adherence to strict safety and quality guidelines.

Responsibilities

Perform downstream manufacturing operations including chromatography and filtration
Execute purification processes for AAV-based gene therapy products
Monitor critical process parameters and perform in-process quality control checks

Skills

Qualifications

Bachelor's Degree in BiologyBachelor's Degree in BiochemistryBachelor's Degree in Biomedical Engineering

About Forge Biologics

forgebiologics.com

Headquarters

Columbus, Ohio, United States

Company Size

201-500 employees

Founded

2020

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Forge Biologics is a CDMO focused on accelerating gene therapy manufacturing, specializing in high‑yield adeno‑associated virus (AAV) vector production. The company offers end‑to‑end services including process and analytical development, clinical‑to‑commercial cGMP manufacturing at a world‑class facility, and regulatory and supply‑chain support. Clients partner with Forge for scalable AAV capacity, technical expertise, and seamless program support to move therapies faster toward patients.