Technical Writer I

Job Description

Job Description

Company Overview

At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful : to enable access to life-changing gene therapies and help bring them from idea into reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities — all united by one goal : improving lives. If you're driven by purpose and excited to make a tangible impact, this is where your journey begins.

Our team works out of The Hearth, a state-of-the-art, 200,000-square-foot cGMP facility in Columbus, Ohio. Here, you won't just watch innovation happen — you'll be part of it. Whether you're scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting complex technical projects, you'll play a key role in bringing hope to patients with genetic diseases.

About the Role

As a Technical Writer, you will play a key role in developing clear, accurate, and well-organized documentation to support the Technical Operations teams at our Columbus facility.

In this cross-functional role, you'll partner with subject matter experts and fellow technical writers to create critical procedural documents that are both effective and compliant—ensuring alignment with Good Manufacturing Practices (GMP), regulatory standards (e.g., FDA), and internal quality requirements.

What You'll Do

• Write, edit, and maintain a variety of technical documents, including standard operating procedures (SOPs), work instructions (WIs), and batch records.
• Organize and streamline written procedures and forms to improve usability and comprehension.
• Collaborate with scientists, engineers, and subject matter experts (SMEs) to gather detailed technical information through interviews and hands-on observation.
• Translate complex technical concepts into clear, accessible content tailored to specific audiences and applications.
• Partner with cross-functional teams to gain a comprehensive understanding of the company's manufacturing processes, technologies, and products.
• Review and revise documents for grammatical accuracy, technical precision, regulatory compliance, and consistency with internal quality standards.
• Maintain consistent formatting, structure, terminology, and tone across all document types in accordance with established templates and style guidelines.
• Identify redundancies, content gaps, and inconsistencies in documentation—proposing improvements based on research and SME input.
• Enhance documentation with visual aids, such as photographs, diagrams, process flows, charts, maps, and other illustrations, to clarify complex procedures.
• Track documentation throughout its lifecycle, facilitating collaboration among applicable departments regarding ongoing document projects.
• Study and interpret drawings, specifications, mockups, and product samples to accurately develop procedures for relevant production methods and technologies.
• Extract key information from manufacturer manuals, trade catalogs, and other resources to support operational and maintenance documentation for onsite equipment.
• Communicate with external stakeholders, such as client representatives, vendors, and publishers, to validate and clarify technical content when necessary.

What You'll Bring

Work Environment and Physical Demands

This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing / sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area.

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned.

Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Forge Your Future with Us

What sets Forge apart is our culture of H.O.P.E. We are hardworking , showing up each day with determination and grit. We are open , creating a space where ideas flow freely and every voice is valued. We are purpose-driven , with every task directly tied to changing lives. And we are engaged , energized by the challenges we face and the milestones we achieve together.

At Forge, your growth matters. We're committed to helping you expand your skills, take on new challenges, and develop your career through mentorship, hands-on learning, and opportunities for advancement. Our people are our greatest investment, and we're proud to see team members grow with us.

If you're ready to use your talent to help deliver hope to patients around the world, join us — and be part of something bigger than yourself.

We've Got You Covered

We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly Un FORGE ttable.