Teams at Forge Biologics

Develops, optimizes, validates, and executes protein-based assays supporting AAV gene therapy products. Responsibilities include troubleshooting, data analysis, assay transfer, quality control, regulatory documentation, mentoring junior staff, project planning, and continuous process improvement in laboratory and cGMP environments.

The Senior Associate Scientist leads scientific and technical documentation projects across QC functions, including SOPs, protocols, and reports. Responsibilities include coordinating with subject matter experts, managing cross-functional documentation projects, updating materials for method qualification and change controls, reviewing quality and consistency, identifying documentation gaps, mentoring junior associates, and administering Veeva Vault processes.

Supports downstream process development for AAV purification under supervision. Performs foundational purification activities including buffer preparation, filtration, chromatography, buffer exchange, clarification, equipment sanitization, and monitoring. Documents experiments, analyzes data, prepares reports and presentations, follows safety and cGMP requirements, and collaborates with cross-functional teams in a laboratory environment.