Technician I, GMP Manufacturing Support - Buffers (3rd Shift)

Forge Your Future with Us: 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 ideas 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. 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. About The Role: The Technician I, GMP Support – Buffers , performs a wide range of functions crucial to AAV gene therapy production. This position is responsible for contributing to buffer and media formulation. This entry-level position offers an opportunity to gain foundational experience in the multifaceted support activities crucial for the production of AAV gene therapy products. Responsibilities: Assist in media and buffer preparation under supervision, adhering to schedules, and maintaining accurate documentation to ensure compliance with SOPs and cGMP regulations. Maintain real-time and accurate documentation; perform the manufacturing review of logbooks, MPR’s, and associated documents. Assist in troubleshooting and resolving minor equipment or process-related issues under the guidance of senior team members. Collaborate with cross-functional teams, including GMP Manufacturing, Quality Assurance, Quality Control, and Product Development, to support efficient manufacturing operations. Assist in equipment setup, inventory management, and material requests for cleaning and manufacturing activities. Adhere to strict GMP gowning procedures, including the use of sterile coveralls, boots, hair net, face covering, goggles, and gloves to prevent contamination and ensure compliance with regulatory standards for cleanroom environments. Contribute to process improvement initiatives, providing feedback and suggestions to enhance department-related processes and improve efficiency. Follow safety procedures and maintain a clean workspace. Qualifications: High school diploma or equivalent required. Experience following SOPs or other protocols/work instructions. Basic computer skills and the ability to learn and use manufacturing software. Ability to work the hours necessary to support production and/or product transfer activities. Ability to work in loud noise environments and in Personal Protective Equipment (PPE) as needed. Ability to work a 3rd shift: 4 x 10-hour schedule (beginning Sunday night and ending Thursday morning), with the flexibility for occasional overtime as needed. Preferred Skills: Prior experience in a regulated- manufacturing or laboratory environment. Exposure to facility or equipment cleaning and sanitization, media and buffer preparation, or equipment building and setup. This…