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Manager, Document Control - QA Operations at Forge Biologics - ApplyBlast

Manager, Document Control - QA Operations

Forge Biologics

2 months ago

4.1 on Glassdoor

Columbus, Ohio, United States

Onsite

Full Time

Manager

0 applicants

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About this role

The Manager, Document Control leads the Document Control team in a GMP‑regulated environment, overseeing the issuance, maintenance, and lifecycle of controlled documents using an electronic quality management system. This role ensures compliance, supports manufacturing and quality functions, and drives continuous improvement through cross‑functional collaboration and regulatory readiness.

Responsibilities

Lead and develop the Document Control team
Manage document change controls and lifecycle in the eQMS
Oversee issuance and maintenance of controlled documents for operations

Skills

About Forge Biologics

forgebiologics.com

Headquarters

Columbus, Ohio, United States

Company Size

201-500 employees

Founded

2020

View Profile

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.